CN1120226C - 含中链支化伯烷基聚氧化烯表面活性剂的漂白洗涤剂组合物 - Google Patents

含中链支化伯烷基聚氧化烯表面活性剂的漂白洗涤剂组合物 Download PDF

Info

Publication number: CN1120226C
Authority: CN; China
Prior art keywords: ethoxylate; integer; alkyl; alcohol ethoxylate; methyl
Prior art date: 1996-11-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CN97181417A

Other languages

English (en)

Chinese (zh)

Other versions

CN1244892A (zh

Inventor

T·A·克里佩

D·S·康诺尔

P·K·温森

J·C·T·R·布尔克特-圣劳伦特

K·W·维尔曼

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Procter and Gamble Ltd

Original Assignee

Procter and Gamble Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-11-26

Filing date

1997-11-19

Publication date

2003-09-03

1997-11-19 Application filed by Procter and Gamble Ltd filed Critical Procter and Gamble Ltd

2000-02-16 Publication of CN1244892A publication Critical patent/CN1244892A/zh

2003-09-03 Application granted granted Critical

2003-09-03 Publication of CN1120226C publication Critical patent/CN1120226C/zh

2017-11-19 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000004094 surface-active agent Substances 0.000 title claims abstract description 130
239000000203 mixture Substances 0.000 claims abstract description 453
125000000217 alkyl group Chemical group 0.000 claims abstract description 169
239000003599 detergent Substances 0.000 claims abstract description 157
238000004140 cleaning Methods 0.000 claims abstract description 51
-1 ethoxy, propoxy Chemical group 0.000 claims description 266
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 120
239000003795 chemical substances by application Substances 0.000 claims description 78
102000004190 Enzymes Human genes 0.000 claims description 59
108090000790 Enzymes Proteins 0.000 claims description 59
150000001875 compounds Chemical class 0.000 claims description 57
229910052739 hydrogen Inorganic materials 0.000 claims description 49
239000001257 hydrogen Substances 0.000 claims description 48
238000007046 ethoxylation reaction Methods 0.000 claims description 47
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 43
125000004432 carbon atom Chemical group C* 0.000 claims description 38
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 38
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 37
229960000541 cetyl alcohol Drugs 0.000 claims description 36
239000003945 anionic surfactant Substances 0.000 claims description 22
125000003545 alkoxy group Chemical group 0.000 claims description 19
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 19
239000007844 bleaching agent Substances 0.000 claims description 17
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
239000012190 activator Substances 0.000 claims description 10
239000002689 soil Substances 0.000 claims description 10
239000004615 ingredient Substances 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
150000002431 hydrogen Chemical class 0.000 claims description 8
239000003112 inhibitor Substances 0.000 claims description 6
239000002736 nonionic surfactant Substances 0.000 claims description 6
230000000996 additive effect Effects 0.000 claims description 3
230000007797 corrosion Effects 0.000 claims description 3
238000005260 corrosion Methods 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
229920000620 organic polymer Polymers 0.000 claims description 3
REIUXOLGHVXAEO-UHFFFAOYSA-N pentadecan-1-ol Chemical compound CCCCCCCCCCCCCCCO REIUXOLGHVXAEO-UHFFFAOYSA-N 0.000 claims 7
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 6
CRXZDFBSTYFRIG-UHFFFAOYSA-N 10-methylpentadecan-1-ol Chemical compound CCCCCC(C)CCCCCCCCCO CRXZDFBSTYFRIG-UHFFFAOYSA-N 0.000 claims 2
ZYUUMAFOCZAAJV-UHFFFAOYSA-N 11-methylpentadecan-1-ol Chemical compound CCCCC(C)CCCCCCCCCCO ZYUUMAFOCZAAJV-UHFFFAOYSA-N 0.000 claims 2
CIUGEUVAWSWBTB-UHFFFAOYSA-N 12-methylpentadecan-1-ol Chemical compound CCCC(C)CCCCCCCCCCCO CIUGEUVAWSWBTB-UHFFFAOYSA-N 0.000 claims 2
HZHCYXMBQIANDP-UHFFFAOYSA-N 3-methylpentadecan-1-ol Chemical compound CCCCCCCCCCCCC(C)CCO HZHCYXMBQIANDP-UHFFFAOYSA-N 0.000 claims 2
USCAIUBWMLHYMF-UHFFFAOYSA-N 4-methylpentadecan-1-ol Chemical compound CCCCCCCCCCCC(C)CCCO USCAIUBWMLHYMF-UHFFFAOYSA-N 0.000 claims 2
QLPBYYNKEZROCN-UHFFFAOYSA-N 5-methylpentadecan-1-ol Chemical compound CCCCCCCCCCC(C)CCCCO QLPBYYNKEZROCN-UHFFFAOYSA-N 0.000 claims 2
QITMGEIDLGSWJI-UHFFFAOYSA-N 6-methylpentadecan-1-ol Chemical compound CCCCCCCCCC(C)CCCCCO QITMGEIDLGSWJI-UHFFFAOYSA-N 0.000 claims 2
AATDUADOOPBKAU-UHFFFAOYSA-N 7-methylpentadecan-1-ol Chemical compound CCCCCCCCC(C)CCCCCCO AATDUADOOPBKAU-UHFFFAOYSA-N 0.000 claims 2
OYDBJGVJQMXASR-UHFFFAOYSA-N 8-methylpentadecan-1-ol Chemical compound CCCCCCCC(C)CCCCCCCO OYDBJGVJQMXASR-UHFFFAOYSA-N 0.000 claims 2
OJHUUXKGMSEIAL-UHFFFAOYSA-N 9-methylpentadecan-1-ol Chemical compound CCCCCCC(C)CCCCCCCCO OJHUUXKGMSEIAL-UHFFFAOYSA-N 0.000 claims 2
JWIWHDBXJLJNPH-UHFFFAOYSA-N 13-methylpentadecan-1-ol Chemical compound CCC(C)CCCCCCCCCCCCO JWIWHDBXJLJNPH-UHFFFAOYSA-N 0.000 claims 1
MVYPKRADYPIKKS-UHFFFAOYSA-N 2,10-dimethylpentadecan-1-ol Chemical compound CCCCCC(C)CCCCCCCC(C)CO MVYPKRADYPIKKS-UHFFFAOYSA-N 0.000 claims 1
SUECHUSKTKVWII-UHFFFAOYSA-N 2,11-dimethylpentadecan-1-ol Chemical compound CCCCC(C)CCCCCCCCC(C)CO SUECHUSKTKVWII-UHFFFAOYSA-N 0.000 claims 1
XKCHTVOKIYIWDN-UHFFFAOYSA-N 2,12-dimethylpentadecan-1-ol Chemical compound CCCC(C)CCCCCCCCCC(C)CO XKCHTVOKIYIWDN-UHFFFAOYSA-N 0.000 claims 1
UTJVUJVUBBPPGM-UHFFFAOYSA-N 2,13-dimethylpentadecan-1-ol Chemical compound CCC(C)CCCCCCCCCCC(C)CO UTJVUJVUBBPPGM-UHFFFAOYSA-N 0.000 claims 1
MWNWEQHHASAOEU-UHFFFAOYSA-N 2,3-dimethylpentadecan-1-ol Chemical compound CCCCCCCCCCCCC(C)C(C)CO MWNWEQHHASAOEU-UHFFFAOYSA-N 0.000 claims 1
ZYIFYIQWTWPTEJ-UHFFFAOYSA-N 2,4-dimethylpentadecan-1-ol Chemical compound CCCCCCCCCCCC(C)CC(C)CO ZYIFYIQWTWPTEJ-UHFFFAOYSA-N 0.000 claims 1
SDMUDPFAXZEOLC-UHFFFAOYSA-N 2,5-dimethylpentadecan-1-ol Chemical compound CCCCCCCCCCC(C)CCC(C)CO SDMUDPFAXZEOLC-UHFFFAOYSA-N 0.000 claims 1
BJOQVMRLMCFVMF-UHFFFAOYSA-N 2,6-dimethylpentadecan-1-ol Chemical compound CCCCCCCCCC(C)CCCC(C)CO BJOQVMRLMCFVMF-UHFFFAOYSA-N 0.000 claims 1
YENWQWYLHJTAQB-UHFFFAOYSA-N 2,7-dimethylpentadecan-1-ol Chemical compound CCCCCCCCC(C)CCCCC(C)CO YENWQWYLHJTAQB-UHFFFAOYSA-N 0.000 claims 1
OVFVOONETFEMQT-UHFFFAOYSA-N 2,8-dimethylpentadecan-1-ol Chemical compound CCCCCCCC(C)CCCCCC(C)CO OVFVOONETFEMQT-UHFFFAOYSA-N 0.000 claims 1
KRWVIVSNXFPYJB-UHFFFAOYSA-N 2,9-dimethylpentadecan-1-ol Chemical compound CCCCCCC(C)CCCCCCC(C)CO KRWVIVSNXFPYJB-UHFFFAOYSA-N 0.000 claims 1
COTCQLIJYALEFP-UHFFFAOYSA-N 3-methylhexadecan-1-ol Chemical compound CCCCCCCCCCCCCC(C)CCO COTCQLIJYALEFP-UHFFFAOYSA-N 0.000 claims 1
ODDVOCXSLXTIIU-UHFFFAOYSA-N 4-Methylpentadecane Chemical compound CCCCCCCCCCCC(C)CCC ODDVOCXSLXTIIU-UHFFFAOYSA-N 0.000 claims 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
238000006213 oxygenation reaction Methods 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 87
229910001868 water Inorganic materials 0.000 abstract description 86
239000007788 liquid Substances 0.000 abstract description 75
238000000034 method Methods 0.000 abstract description 65
238000009472 formulation Methods 0.000 abstract description 7
238000005406 washing Methods 0.000 description 181
239000000463 material Substances 0.000 description 96
239000000047 product Substances 0.000 description 86
239000013543 active substance Substances 0.000 description 80
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 72
229910052799 carbon Inorganic materials 0.000 description 71
229940088598 enzyme Drugs 0.000 description 57
238000002360 preparation method Methods 0.000 description 46
150000002500 ions Chemical class 0.000 description 45
150000001721 carbon Chemical group 0.000 description 44
239000002253 acid Substances 0.000 description 43
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 42
239000011734 sodium Substances 0.000 description 42
150000003839 salts Chemical class 0.000 description 41
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 37
229910052757 nitrogen Inorganic materials 0.000 description 37
239000002245 particle Substances 0.000 description 36
229910021653 sulphate ion Inorganic materials 0.000 description 36
230000003287 optical effect Effects 0.000 description 34
150000001336 alkenes Chemical class 0.000 description 32
108010065511 Amylases Proteins 0.000 description 31
102000013142 Amylases Human genes 0.000 description 31
235000019418 amylase Nutrition 0.000 description 31
239000004382 Amylase Substances 0.000 description 30
239000004744 fabric Substances 0.000 description 30
229910052708 sodium Inorganic materials 0.000 description 30
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 29
150000001412 amines Chemical class 0.000 description 29
239000003921 oil Substances 0.000 description 29
235000019198 oils Nutrition 0.000 description 28
239000002585 base Substances 0.000 description 27
108091005804 Peptidases Proteins 0.000 description 26
102000035195 Peptidases Human genes 0.000 description 26
239000000975 dye Substances 0.000 description 26
239000007791 liquid phase Substances 0.000 description 26
239000000126 substance Substances 0.000 description 26
230000002087 whitening effect Effects 0.000 description 26
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
229920001296 polysiloxane Polymers 0.000 description 24
229920003171 Poly (ethylene oxide) Polymers 0.000 description 23
230000000694 effects Effects 0.000 description 23
230000002209 hydrophobic effect Effects 0.000 description 23
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 22
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 22
150000002148 esters Chemical class 0.000 description 22
238000003756 stirring Methods 0.000 description 22
102000004882 Lipase Human genes 0.000 description 21
108090001060 Lipase Proteins 0.000 description 21
239000004367 Lipase Substances 0.000 description 21
229910021536 Zeolite Inorganic materials 0.000 description 21
239000003054 catalyst Substances 0.000 description 21
238000006243 chemical reaction Methods 0.000 description 21
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 21
235000019421 lipase Nutrition 0.000 description 21
229940040461 lipase Drugs 0.000 description 21
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
239000010457 zeolite Substances 0.000 description 21
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 20
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 20
238000009826 distribution Methods 0.000 description 20
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 19
239000004064 cosurfactant Substances 0.000 description 19
239000006260 foam Substances 0.000 description 19
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 19
239000012071 phase Substances 0.000 description 19
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 18
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
125000003342 alkenyl group Chemical group 0.000 description 18
238000004061 bleaching Methods 0.000 description 18
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 18
239000007859 condensation product Substances 0.000 description 18
229940075933 dithionate Drugs 0.000 description 17
PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol Substances OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 17
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 16
239000000243 solution Substances 0.000 description 16
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 16
238000012546 transfer Methods 0.000 description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 15
239000011575 calcium Substances 0.000 description 15
229920000642 polymer Polymers 0.000 description 15
229910052700 potassium Inorganic materials 0.000 description 15
239000000843 powder Substances 0.000 description 15
239000002904 solvent Substances 0.000 description 15
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 14
150000008051 alkyl sulfates Chemical class 0.000 description 14
150000002191 fatty alcohols Chemical class 0.000 description 14
229930195733 hydrocarbon Natural products 0.000 description 14
150000002430 hydrocarbons Chemical class 0.000 description 14
239000011591 potassium Substances 0.000 description 14
239000011541 reaction mixture Substances 0.000 description 14
238000003786 synthesis reaction Methods 0.000 description 14
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 13
239000004215 Carbon black (E152) Substances 0.000 description 13
108010059892 Cellulase Proteins 0.000 description 13
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 13
150000001298 alcohols Chemical class 0.000 description 13
150000004996 alkyl benzenes Chemical class 0.000 description 13
230000015572 biosynthetic process Effects 0.000 description 13
229940106157 cellulase Drugs 0.000 description 13
235000014113 dietary fatty acids Nutrition 0.000 description 13
239000006185 dispersion Substances 0.000 description 13
238000005516 engineering process Methods 0.000 description 13
239000000194 fatty acid Substances 0.000 description 13
229930195729 fatty acid Natural products 0.000 description 13
238000005984 hydrogenation reaction Methods 0.000 description 13
239000000344 soap Substances 0.000 description 13
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 12
239000003085 diluting agent Substances 0.000 description 12
239000007787 solid Substances 0.000 description 12
235000013599 spices Nutrition 0.000 description 12
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
244000060011 Cocos nucifera Species 0.000 description 11
235000013162 Cocos nucifera Nutrition 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 11
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 11
230000008859 change Effects 0.000 description 11
239000000460 chlorine Substances 0.000 description 11
229940048961 cholinesterase Drugs 0.000 description 11
239000007789 gas Substances 0.000 description 11
150000002632 lipids Chemical class 0.000 description 11
239000011572 manganese Substances 0.000 description 11
239000000178 monomer Substances 0.000 description 11
238000010926 purge Methods 0.000 description 11
230000003019 stabilising effect Effects 0.000 description 11
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
102000003914 Cholinesterases Human genes 0.000 description 10
108090000322 Cholinesterases Proteins 0.000 description 10
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 10
229920002125 Sokalan® Polymers 0.000 description 10
230000008901 benefit Effects 0.000 description 10
239000003153 chemical reaction reagent Substances 0.000 description 10
229910052801 chlorine Inorganic materials 0.000 description 10
229910052760 oxygen Inorganic materials 0.000 description 10
239000012188 paraffin wax Substances 0.000 description 10
239000011236 particulate material Substances 0.000 description 10
229920001451 polypropylene glycol Polymers 0.000 description 10
239000004575 stone Substances 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
239000000470 constituent Substances 0.000 description 9
238000004851 dishwashing Methods 0.000 description 9
150000004665 fatty acids Chemical class 0.000 description 9
239000001301 oxygen Substances 0.000 description 9
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 9
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 9
230000019635 sulfation Effects 0.000 description 9
238000005670 sulfation reaction Methods 0.000 description 9
WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 8
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 8
102000003992 Peroxidases Human genes 0.000 description 8
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 8
125000001931 aliphatic group Chemical group 0.000 description 8
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
239000004927 clay Substances 0.000 description 8
229910017052 cobalt Inorganic materials 0.000 description 8
239000010941 cobalt Substances 0.000 description 8
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 8
238000009833 condensation Methods 0.000 description 8
230000005494 condensation Effects 0.000 description 8
238000004519 manufacturing process Methods 0.000 description 8
230000035772 mutation Effects 0.000 description 8
229940072417 peroxidase Drugs 0.000 description 8
108040007629 peroxidase activity proteins Proteins 0.000 description 8
230000008569 process Effects 0.000 description 8
239000002516 radical scavenger Substances 0.000 description 8
239000002994 raw material Substances 0.000 description 8
239000003352 sequestering agent Substances 0.000 description 8
239000000377 silicon dioxide Substances 0.000 description 8
229910052938 sodium sulfate Inorganic materials 0.000 description 8
235000011152 sodium sulphate Nutrition 0.000 description 8
230000002194 synthesizing effect Effects 0.000 description 8
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 8
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
239000004698 Polyethylene Substances 0.000 description 7
238000013019 agitation Methods 0.000 description 7
150000003863 ammonium salts Chemical class 0.000 description 7
125000003118 aryl group Chemical group 0.000 description 7
229910052728 basic metal Inorganic materials 0.000 description 7
150000003818 basic metals Chemical class 0.000 description 7
125000002091 cationic group Chemical group 0.000 description 7
238000001816 cooling Methods 0.000 description 7
229920001577 copolymer Polymers 0.000 description 7
239000013078 crystal Substances 0.000 description 7
229960001760 dimethyl sulfoxide Drugs 0.000 description 7
239000008187 granular material Substances 0.000 description 7
125000002768 hydroxyalkyl group Chemical group 0.000 description 7
230000005764 inhibitory process Effects 0.000 description 7
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 7
239000011159 matrix material Substances 0.000 description 7
238000002156 mixing Methods 0.000 description 7
230000001590 oxidative effect Effects 0.000 description 7
238000012545 processing Methods 0.000 description 7
230000009467 reduction Effects 0.000 description 7
238000006722 reduction reaction Methods 0.000 description 7
235000019832 sodium triphosphate Nutrition 0.000 description 7
BVUGCDWHWUYLII-UHFFFAOYSA-N 6-hydroxyhexyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCCCCO)C1=CC=CC=C1 BVUGCDWHWUYLII-UHFFFAOYSA-N 0.000 description 6
JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical group OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
229910004298 SiO 2 Inorganic materials 0.000 description 6
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
125000002252 acyl group Chemical group 0.000 description 6
125000002877 alkyl aryl group Chemical group 0.000 description 6
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 6
230000031709 bromination Effects 0.000 description 6
238000005893 bromination reaction Methods 0.000 description 6
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 6
239000000284 extract Substances 0.000 description 6
239000008103 glucose Substances 0.000 description 6
235000011187 glycerol Nutrition 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
239000011777 magnesium Substances 0.000 description 6
239000002480 mineral oil Substances 0.000 description 6
235000010446 mineral oil Nutrition 0.000 description 6
239000003495 polar organic solvent Substances 0.000 description 6
229920000768 polyamine Polymers 0.000 description 6
229920000728 polyester Polymers 0.000 description 6
125000001453 quaternary ammonium group Chemical group 0.000 description 6
230000002829 reductive effect Effects 0.000 description 6
238000011160 research Methods 0.000 description 6
229960001866 silicon dioxide Drugs 0.000 description 6
239000002002 slurry Substances 0.000 description 6
159000000000 sodium salts Chemical class 0.000 description 6
108010075550 termamyl Proteins 0.000 description 6
238000003828 vacuum filtration Methods 0.000 description 6
239000004711 α-olefin Substances 0.000 description 6
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 5
241000193830 Bacillus <bacterium> Species 0.000 description 5
BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 5
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 5
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 5
150000001299 aldehydes Chemical class 0.000 description 5
239000003513 alkali Substances 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 5
229910052791 calcium Inorganic materials 0.000 description 5
150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
230000004927 fusion Effects 0.000 description 5
239000004519 grease Substances 0.000 description 5
230000006872 improvement Effects 0.000 description 5
229910052500 inorganic mineral Inorganic materials 0.000 description 5
229910052744 lithium Inorganic materials 0.000 description 5
229910052748 manganese Inorganic materials 0.000 description 5
235000010755 mineral Nutrition 0.000 description 5
239000011707 mineral Substances 0.000 description 5
238000007254 oxidation reaction Methods 0.000 description 5
238000012856 packing Methods 0.000 description 5
229920000058 polyacrylate Polymers 0.000 description 5
229920001223 polyethylene glycol Polymers 0.000 description 5
229920001282 polysaccharide Polymers 0.000 description 5
239000005017 polysaccharide Substances 0.000 description 5
229920006395 saturated elastomer Polymers 0.000 description 5
150000003333 secondary alcohols Chemical class 0.000 description 5
235000012239 silicon dioxide Nutrition 0.000 description 5
235000017550 sodium carbonate Nutrition 0.000 description 5
229910000029 sodium carbonate Inorganic materials 0.000 description 5
239000000758 substrate Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 4
YAXXOCZAXKLLCV-UHFFFAOYSA-N 3-dodecyloxolane-2,5-dione Chemical class CCCCCCCCCCCCC1CC(=O)OC1=O YAXXOCZAXKLLCV-UHFFFAOYSA-N 0.000 description 4
YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 4
ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 4
229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
235000008733 Citrus aurantifolia Nutrition 0.000 description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
102220644676 Galectin-related protein_D96L_mutation Human genes 0.000 description 4
239000007818 Grignard reagent Substances 0.000 description 4
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 4
150000001204 N-oxides Chemical class 0.000 description 4
101710194948 Protein phosphatase PhpP Proteins 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
JKOQMXDAZYYFNH-UHFFFAOYSA-N S(=O)(=O)(O)O.C(CCCCCCCCCCCCCCC(C)C)[Na] Chemical compound S(=O)(=O)(O)O.C(CCCCCCCCCCCCCCC(C)C)[Na] JKOQMXDAZYYFNH-UHFFFAOYSA-N 0.000 description 4
241000223258 Thermomyces lanuginosus Species 0.000 description 4
235000011941 Tilia x europaea Nutrition 0.000 description 4
238000005054 agglomeration Methods 0.000 description 4
230000002776 aggregation Effects 0.000 description 4
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
150000001413 amino acids Chemical group 0.000 description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
235000010338 boric acid Nutrition 0.000 description 4
239000004327 boric acid Substances 0.000 description 4
229960002645 boric acid Drugs 0.000 description 4
229910001424 calcium ion Inorganic materials 0.000 description 4
238000006555 catalytic reaction Methods 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
230000018044 dehydration Effects 0.000 description 4
238000006297 dehydration reaction Methods 0.000 description 4
238000000280 densification Methods 0.000 description 4
238000011161 development Methods 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
238000006471 dimerization reaction Methods 0.000 description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
QDPMLKBAQOZXEF-UHFFFAOYSA-N ethanesulfonic acid;sodium Chemical compound [Na].CCS(O)(=O)=O QDPMLKBAQOZXEF-UHFFFAOYSA-N 0.000 description 4
235000019197 fats Nutrition 0.000 description 4
239000000835 fiber Substances 0.000 description 4
238000001914 filtration Methods 0.000 description 4
239000000796 flavoring agent Substances 0.000 description 4
235000019634 flavors Nutrition 0.000 description 4
JPZROSNLRWHSQQ-UHFFFAOYSA-N furan-2,5-dione;prop-2-enoic acid Chemical compound OC(=O)C=C.O=C1OC(=O)C=C1 JPZROSNLRWHSQQ-UHFFFAOYSA-N 0.000 description 4
239000011521 glass Substances 0.000 description 4
125000003147 glycosyl group Chemical group 0.000 description 4
150000004795 grignard reagents Chemical class 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
125000001165 hydrophobic group Chemical group 0.000 description 4
150000002576 ketones Chemical class 0.000 description 4
239000004571 lime Substances 0.000 description 4
239000006210 lotion Substances 0.000 description 4
125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 4
150000004702 methyl esters Chemical class 0.000 description 4
230000003647 oxidation Effects 0.000 description 4
HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 4
239000002304 perfume Substances 0.000 description 4
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 4
229910052697 platinum Inorganic materials 0.000 description 4
239000002798 polar solvent Substances 0.000 description 4
229920000573 polyethylene Polymers 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
239000011347 resin Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
229920002545 silicone oil Polymers 0.000 description 4
239000012312 sodium hydride Substances 0.000 description 4
229910000104 sodium hydride Inorganic materials 0.000 description 4
235000010339 sodium tetraborate Nutrition 0.000 description 4
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 4
239000003760 tallow Substances 0.000 description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 4
230000008719 thickening Effects 0.000 description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
238000005809 transesterification reaction Methods 0.000 description 4
230000017105 transposition Effects 0.000 description 4
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
229960004418 trolamine Drugs 0.000 description 4
VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 3
OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 3
CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 3
FCMCSZXRVWDVAW-UHFFFAOYSA-N 6-bromo-1-hexanol Chemical compound OCCCCCCBr FCMCSZXRVWDVAW-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
229910017090 AlO 2 Inorganic materials 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
241000194108 Bacillus licheniformis Species 0.000 description 3
241000894006 Bacteria Species 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
229910020366 ClO 4 Inorganic materials 0.000 description 3
DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 3
101001001462 Homo sapiens Importin subunit alpha-5 Proteins 0.000 description 3
102000004157 Hydrolases Human genes 0.000 description 3
108090000604 Hydrolases Proteins 0.000 description 3
102100035692 Importin subunit alpha-1 Human genes 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 3
BCXBKOQDEOJNRH-UHFFFAOYSA-N NOP(O)=O Chemical class NOP(O)=O BCXBKOQDEOJNRH-UHFFFAOYSA-N 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
ZUBJEHHGZYTRPH-KTKRTIGZSA-N [(z)-octadec-9-enyl] hydrogen sulfate Chemical compound CCCCCCCC\C=C/CCCCCCCCOS(O)(=O)=O ZUBJEHHGZYTRPH-KTKRTIGZSA-N 0.000 description 3
NZNQMPZXPUKVSQ-UHFFFAOYSA-N [O].C1CO1 Chemical compound [O].C1CO1 NZNQMPZXPUKVSQ-UHFFFAOYSA-N 0.000 description 3
239000003377 acid catalyst Substances 0.000 description 3
238000005882 aldol condensation reaction Methods 0.000 description 3
125000002723 alicyclic group Chemical group 0.000 description 3
125000004183 alkoxy alkyl group Chemical group 0.000 description 3
150000003973 alkyl amines Chemical class 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
108090000637 alpha-Amylases Proteins 0.000 description 3
102000004139 alpha-Amylases Human genes 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
229940077388 benzenesulfonate Drugs 0.000 description 3
229910021538 borax Inorganic materials 0.000 description 3
229910052796 boron Inorganic materials 0.000 description 3
239000000872 buffer Substances 0.000 description 3
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 3
239000001110 calcium chloride Substances 0.000 description 3
229910001628 calcium chloride Inorganic materials 0.000 description 3
235000011148 calcium chloride Nutrition 0.000 description 3
239000001768 carboxy methyl cellulose Substances 0.000 description 3
235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
150000007942 carboxylates Chemical class 0.000 description 3
239000008112 carboxymethyl-cellulose Substances 0.000 description 3
229920002678 cellulose Polymers 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
239000004567 concrete Substances 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 3
230000009849 deactivation Effects 0.000 description 3
238000013461 design Methods 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
239000004205 dimethyl polysiloxane Substances 0.000 description 3
125000004185 ester group Chemical group 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
239000002979 fabric softener Substances 0.000 description 3
239000000945 filler Substances 0.000 description 3
238000005187 foaming Methods 0.000 description 3
230000022244 formylation Effects 0.000 description 3
238000006170 formylation reaction Methods 0.000 description 3
239000000499 gel Substances 0.000 description 3
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
125000001183 hydrocarbyl group Chemical group 0.000 description 3
238000007037 hydroformylation reaction Methods 0.000 description 3
230000007062 hydrolysis Effects 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
230000003165 hydrotropic effect Effects 0.000 description 3
WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 3
230000001965 increasing effect Effects 0.000 description 3
238000005342 ion exchange Methods 0.000 description 3
SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 3
238000004900 laundering Methods 0.000 description 3
238000010412 laundry washing Methods 0.000 description 3
239000012280 lithium aluminium hydride Substances 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
159000000003 magnesium salts Chemical class 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 3
108010020132 microbial serine proteinases Proteins 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
238000006384 oligomerization reaction Methods 0.000 description 3
239000012074 organic phase Substances 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
150000003014 phosphoric acid esters Chemical class 0.000 description 3
XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
239000002243 precursor Substances 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
238000005086 pumping Methods 0.000 description 3
238000001953 recrystallisation Methods 0.000 description 3
238000010992 reflux Methods 0.000 description 3
MSFGZHUJTJBYFA-UHFFFAOYSA-M sodium dichloroisocyanurate Chemical compound [Na+].ClN1C(=O)[N-]C(=O)N(Cl)C1=O MSFGZHUJTJBYFA-UHFFFAOYSA-M 0.000 description 3
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
239000004328 sodium tetraborate Substances 0.000 description 3
239000007790 solid phase Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 3
238000006277 sulfonation reaction Methods 0.000 description 3
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 3
238000010189 synthetic method Methods 0.000 description 3
239000004753 textile Substances 0.000 description 3
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 3
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 3
238000001291 vacuum drying Methods 0.000 description 3
239000000341 volatile oil Substances 0.000 description 3
239000001993 wax Substances 0.000 description 3
150000003751 zinc Chemical class 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
GEWDNTWNSAZUDX-WQMVXFAESA-N (-)-methyl jasmonate Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-WQMVXFAESA-N 0.000 description 2
239000001707 (E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol Substances 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
OQNZFMZDPKAMHH-UHFFFAOYSA-N 1-methoxyethane-1,1,2-tricarboxylic acid Chemical compound COC(C(O)=O)(C(O)=O)CC(O)=O OQNZFMZDPKAMHH-UHFFFAOYSA-N 0.000 description 2
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
SDGKUVSVPIIUCF-UHFFFAOYSA-N 2,6-dimethylpiperidine Chemical compound CC1CCCC(C)N1 SDGKUVSVPIIUCF-UHFFFAOYSA-N 0.000 description 2
MPJQXAIKMSKXBI-UHFFFAOYSA-N 2,7,9,14-tetraoxa-1,8-diazabicyclo[6.6.2]hexadecane-3,6,10,13-tetrone Chemical compound C1CN2OC(=O)CCC(=O)ON1OC(=O)CCC(=O)O2 MPJQXAIKMSKXBI-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
QCYOIFVBYZNUNW-UHFFFAOYSA-N 2-(dimethylazaniumyl)propanoate Chemical compound CN(C)C(C)C(O)=O QCYOIFVBYZNUNW-UHFFFAOYSA-N 0.000 description 2
LUZDYPLAQQGJEA-UHFFFAOYSA-N 2-Methoxynaphthalene Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 description 2
JAONWSWNLZLNFS-UHFFFAOYSA-N 2-[4-(2-phenylethenyl)phenyl]benzo[e]benzotriazole Chemical compound C=1C=C(N2N=C3C4=CC=CC=C4C=CC3=N2)C=CC=1C=CC1=CC=CC=C1 JAONWSWNLZLNFS-UHFFFAOYSA-N 0.000 description 2
XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 2
XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 2
RJWUMFHQJJBBOD-UHFFFAOYSA-N 2-methylheptadecane Chemical compound CCCCCCCCCCCCCCCC(C)C RJWUMFHQJJBBOD-UHFFFAOYSA-N 0.000 description 2
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
BJLRAKFWOUAROE-UHFFFAOYSA-N 2500-83-6 Chemical compound C12C=CCC2C2CC(OC(=O)C)C1C2 BJLRAKFWOUAROE-UHFFFAOYSA-N 0.000 description 2
FAGGUIDTQQXDSJ-UHFFFAOYSA-N 3-benzoylazepan-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCNC1=O FAGGUIDTQQXDSJ-UHFFFAOYSA-N 0.000 description 2
BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical compound NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 description 2
LWYAUHJRUCQFCX-UHFFFAOYSA-N 4-dodecoxy-4-oxobutanoic acid Chemical compound CCCCCCCCCCCCOC(=O)CCC(O)=O LWYAUHJRUCQFCX-UHFFFAOYSA-N 0.000 description 2
LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 2
JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 description 2
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
241000193744 Bacillus amyloliquefaciens Species 0.000 description 2
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
101100148128 Caenorhabditis elegans rsp-4 gene Proteins 0.000 description 2
229910021532 Calcite Inorganic materials 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
241000640882 Condea Species 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
241000282326 Felis catus Species 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
238000003747 Grignard reaction Methods 0.000 description 2
FFVHXGZXDRXFLQ-UHFFFAOYSA-N Hydroxy-cyclopentadecan Natural products OC1CCCCCCCCCCCCCC1 FFVHXGZXDRXFLQ-UHFFFAOYSA-N 0.000 description 2
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 2
244000178870 Lavandula angustifolia Species 0.000 description 2
235000010663 Lavandula angustifolia Nutrition 0.000 description 2
235000015511 Liquidambar orientalis Nutrition 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
BLUHKGOSFDHHGX-UHFFFAOYSA-N Phytol Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)C=CO BLUHKGOSFDHHGX-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
229920000805 Polyaspartic acid Polymers 0.000 description 2
241000589516 Pseudomonas Species 0.000 description 2
OEYQBKYISMRWQB-UHFFFAOYSA-N Santal Chemical compound C=1C(OC)=CC(O)=C(C2=O)C=1OC=C2C1=CC=C(O)C(O)=C1 OEYQBKYISMRWQB-UHFFFAOYSA-N 0.000 description 2
239000004902 Softening Agent Substances 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
239000004870 Styrax Substances 0.000 description 2
244000028419 Styrax benzoin Species 0.000 description 2
235000000126 Styrax benzoin Nutrition 0.000 description 2
108010056079 Subtilisins Proteins 0.000 description 2
102000005158 Subtilisins Human genes 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
HNZBNQYXWOLKBA-UHFFFAOYSA-N Tetrahydrofarnesol Natural products CC(C)CCCC(C)CCCC(C)=CCO HNZBNQYXWOLKBA-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
239000004473 Threonine Substances 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
AKAARPDHDDFMLL-UHFFFAOYSA-N [Ca].[K].[C] Chemical compound [Ca].[K].[C] AKAARPDHDDFMLL-UHFFFAOYSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
230000009471 action Effects 0.000 description 2
125000003158 alcohol group Chemical group 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000008052 alkyl sulfonates Chemical class 0.000 description 2
125000005466 alkylenyl group Chemical group 0.000 description 2
BOTWFXYSPFMFNR-OALUTQOASA-N all-rac-phytol Natural products CC(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)=CCO BOTWFXYSPFMFNR-OALUTQOASA-N 0.000 description 2
229940024171 alpha-amylase Drugs 0.000 description 2
GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 2
GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 2
239000004411 aluminium Substances 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
229940024606 amino acid Drugs 0.000 description 2
235000001014 amino acid Nutrition 0.000 description 2
239000003429 antifungal agent Substances 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
230000003078 antioxidant effect Effects 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
239000011324 bead Substances 0.000 description 2
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
230000001851 biosynthetic effect Effects 0.000 description 2
235000014121 butter Nutrition 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
239000000920 calcium hydroxide Substances 0.000 description 2
229910001861 calcium hydroxide Inorganic materials 0.000 description 2
159000000007 calcium salts Chemical class 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
229910052663 cancrinite Inorganic materials 0.000 description 2
SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 description 2
239000002738 chelating agent Substances 0.000 description 2
HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
239000002131 composite material Substances 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 description 2
230000008021 deposition Effects 0.000 description 2
AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 2
230000002478 diastatic effect Effects 0.000 description 2
GSPKZYJPUDYKPI-UHFFFAOYSA-N diethoxy sulfate Chemical compound CCOOS(=O)(=O)OOCC GSPKZYJPUDYKPI-UHFFFAOYSA-N 0.000 description 2
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 2
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
229960001484 edetic acid Drugs 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
235000019439 ethyl acetate Nutrition 0.000 description 2
229940071087 ethylenediamine disuccinate Drugs 0.000 description 2
239000012530 fluid Substances 0.000 description 2
239000002803 fossil fuel Substances 0.000 description 2
239000012634 fragment Substances 0.000 description 2
150000002240 furans Chemical class 0.000 description 2
IFYYFLINQYPWGJ-UHFFFAOYSA-N gamma-decalactone Chemical compound CCCCCCC1CCC(=O)O1 IFYYFLINQYPWGJ-UHFFFAOYSA-N 0.000 description 2
238000007429 general method Methods 0.000 description 2
229930182478 glucoside Natural products 0.000 description 2
150000008131 glucosides Chemical class 0.000 description 2
150000004676 glycans Chemical class 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
229930182470 glycoside Natural products 0.000 description 2
150000002338 glycosides Chemical class 0.000 description 2
229920000578 graft copolymer Polymers 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
230000036571 hydration Effects 0.000 description 2
238000006703 hydration reaction Methods 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
150000002475 indoles Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
238000006317 isomerization reaction Methods 0.000 description 2
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
238000005304 joining Methods 0.000 description 2
239000001102 lavandula vera Substances 0.000 description 2
235000018219 lavender Nutrition 0.000 description 2
235000012204 lemonade/lime carbonate Nutrition 0.000 description 2
CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
238000004811 liquid chromatography Methods 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
229910001425 magnesium ion Inorganic materials 0.000 description 2
238000012423 maintenance Methods 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 2
150000001457 metallic cations Chemical class 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
GEWDNTWNSAZUDX-UHFFFAOYSA-N methyl 7-epi-jasmonate Natural products CCC=CCC1C(CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-UHFFFAOYSA-N 0.000 description 2
UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 2
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 2
CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 2
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
YPJKMVATUPSWOH-UHFFFAOYSA-N nitrooxidanyl Chemical compound [O][N+]([O-])=O YPJKMVATUPSWOH-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000000123 paper Substances 0.000 description 2
DMCJFWXGXUEHFD-UHFFFAOYSA-N pentatriacontan-18-one Chemical compound CCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCC DMCJFWXGXUEHFD-UHFFFAOYSA-N 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical group CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
150000003016 phosphoric acids Chemical class 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
230000002186 photoactivation Effects 0.000 description 2
BOTWFXYSPFMFNR-PYDDKJGSSA-N phytol Chemical compound CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C\CO BOTWFXYSPFMFNR-PYDDKJGSSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
108010064470 polyaspartate Proteins 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000001205 polyphosphate Substances 0.000 description 2
235000011176 polyphosphates Nutrition 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
235000019260 propionic acid Nutrition 0.000 description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
235000018102 proteins Nutrition 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
150000003233 pyrroles Chemical class 0.000 description 2
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
230000000452 restraining effect Effects 0.000 description 2
229920002050 silicone resin Polymers 0.000 description 2
238000002741 site-directed mutagenesis Methods 0.000 description 2
239000001488 sodium phosphate Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
239000008107 starch Substances 0.000 description 2
235000019698 starch Nutrition 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
239000000271 synthetic detergent Substances 0.000 description 2
229920001897 terpolymer Polymers 0.000 description 2
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 2
239000010936 titanium Substances 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
150000003624 transition metals Chemical class 0.000 description 2
REZQBEBOWJAQKS-UHFFFAOYSA-N triacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO REZQBEBOWJAQKS-UHFFFAOYSA-N 0.000 description 2
QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 2
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 2
UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 2
235000019801 trisodium phosphate Nutrition 0.000 description 2
229910000406 trisodium phosphate Inorganic materials 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
229920001567 vinyl ester resin Polymers 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
PLVCYMZAEQRYHJ-UHFFFAOYSA-N (2-bromophenyl)boronic acid Chemical compound OB(O)C1=CC=CC=C1Br PLVCYMZAEQRYHJ-UHFFFAOYSA-N 0.000 description 1
CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 description 1
XINQFOMFQFGGCQ-UHFFFAOYSA-L (2-dodecoxy-2-oxoethyl)-[6-[(2-dodecoxy-2-oxoethyl)-dimethylazaniumyl]hexyl]-dimethylazanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCCOC(=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCC XINQFOMFQFGGCQ-UHFFFAOYSA-L 0.000 description 1
239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
YPZUZOLGGMJZJO-XRGAULLZSA-N (3as,5as,9as,9br)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1h-benzo[e][1]benzofuran Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@@]2(C)OCC1 YPZUZOLGGMJZJO-XRGAULLZSA-N 0.000 description 1
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
JRJBVWJSTHECJK-LUAWRHEFSA-N (z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC(=O)C(\C)=C/C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-LUAWRHEFSA-N 0.000 description 1
LRGXCBHOBRUTJN-UHFFFAOYSA-N 1,1'-biphenyl;sodium Chemical compound [Na].[Na].C1=CC=CC=C1C1=CC=CC=C1 LRGXCBHOBRUTJN-UHFFFAOYSA-N 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
150000000183 1,3-benzoxazoles Chemical class 0.000 description 1
229940058015 1,3-butylene glycol Drugs 0.000 description 1
VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
OVXWHHYDMKASOR-UHFFFAOYSA-N 1-methylcyclohexa-2,4-diene-1-sulfonic acid Chemical compound OS(=O)(=O)C1(C)CC=CC=C1 OVXWHHYDMKASOR-UHFFFAOYSA-N 0.000 description 1
CBJPRTGKMYOVJO-UHFFFAOYSA-N 1-phenyl-2-(2-phenylethenyl)benzene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1C1=CC=CC=C1 CBJPRTGKMYOVJO-UHFFFAOYSA-N 0.000 description 1
OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
HTAKISAXTQLJGM-UHFFFAOYSA-N 2,10-dimethyltetradecan-1-ol Chemical compound CCCCC(C)CCCCCCCC(C)CO HTAKISAXTQLJGM-UHFFFAOYSA-N 0.000 description 1
LOZWNEWHBUXBCA-UHFFFAOYSA-N 2,11-dimethyltetradecan-1-ol Chemical compound CCCC(C)CCCCCCCCC(C)CO LOZWNEWHBUXBCA-UHFFFAOYSA-N 0.000 description 1
RGYRYZQXUBINQA-UHFFFAOYSA-N 2,12-dimethyltetradecan-1-ol Chemical compound CCC(C)CCCCCCCCCC(C)CO RGYRYZQXUBINQA-UHFFFAOYSA-N 0.000 description 1
PEHXXCUSMPZMKS-UHFFFAOYSA-N 2,3-dimethyltetradecan-1-ol Chemical compound CCCCCCCCCCCC(C)C(C)CO PEHXXCUSMPZMKS-UHFFFAOYSA-N 0.000 description 1
VJSWLXWONORKLD-UHFFFAOYSA-N 2,4,6-trihydroxybenzene-1,3,5-trisulfonic acid Chemical compound OC1=C(S(O)(=O)=O)C(O)=C(S(O)(=O)=O)C(O)=C1S(O)(=O)=O VJSWLXWONORKLD-UHFFFAOYSA-N 0.000 description 1
AVJVDWDELKUAKE-UHFFFAOYSA-N 2,4-dimethyltetradecan-1-ol Chemical compound CCCCCCCCCCC(C)CC(C)CO AVJVDWDELKUAKE-UHFFFAOYSA-N 0.000 description 1
FKFSERQPKIYIDW-UHFFFAOYSA-N 2,5-dimethyltetradecan-1-ol Chemical compound CCCCCCCCCC(C)CCC(C)CO FKFSERQPKIYIDW-UHFFFAOYSA-N 0.000 description 1
DRDVHCSNTGTEOH-UHFFFAOYSA-N 2,6-dimethyltetradecan-1-ol Chemical compound CCCCCCCCC(C)CCCC(C)CO DRDVHCSNTGTEOH-UHFFFAOYSA-N 0.000 description 1
DLQBSLQQCAVWDT-UHFFFAOYSA-N 2,7-dimethyltetradecan-1-ol Chemical compound CCCCCCCC(C)CCCCC(C)CO DLQBSLQQCAVWDT-UHFFFAOYSA-N 0.000 description 1
GUTMCTKABIVFAX-UHFFFAOYSA-N 2,8-dimethyltetradecan-1-ol Chemical compound CCCCCCC(C)CCCCCC(C)CO GUTMCTKABIVFAX-UHFFFAOYSA-N 0.000 description 1
HRARMCULBGOAPD-UHFFFAOYSA-N 2,9-dimethyltetradecan-1-ol Chemical compound CCCCCC(C)CCCCCCC(C)CO HRARMCULBGOAPD-UHFFFAOYSA-N 0.000 description 1
XQUNLIWIQNBLOZ-UHFFFAOYSA-N 2-(2-phenylethenyl)benzo[e][1,3]benzoxazole Chemical compound N=1C(C2=CC=CC=C2C=C2)=C2OC=1C=CC1=CC=CC=C1 XQUNLIWIQNBLOZ-UHFFFAOYSA-N 0.000 description 1
AKXGAGZTEMGMHW-UHFFFAOYSA-N 2-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-6-[2-(2-sulfophenyl)ethenyl]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=CC1=CC=CC(NC=2N=C(N=C(NC=3C=CC=CC=3)N=2)N2CCOCC2)=C1S(O)(=O)=O AKXGAGZTEMGMHW-UHFFFAOYSA-N 0.000 description 1
WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 1
UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
GLVYLTSKTCWWJR-UHFFFAOYSA-N 2-carbonoperoxoylbenzoic acid Chemical class OOC(=O)C1=CC=CC=C1C(O)=O GLVYLTSKTCWWJR-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
JJJOZVFVARQUJV-UHFFFAOYSA-N 2-ethylhexylphosphonic acid Chemical compound CCCCC(CC)CP(O)(O)=O JJJOZVFVARQUJV-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 description 1
CJAZCKUGLFWINJ-UHFFFAOYSA-N 3,4-dihydroxybenzene-1,2-disulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C(S(O)(=O)=O)=C1O CJAZCKUGLFWINJ-UHFFFAOYSA-N 0.000 description 1
KWYJDIUEHHCHCZ-UHFFFAOYSA-N 3-[2-[bis(2-carboxyethyl)amino]ethyl-(2-carboxyethyl)amino]propanoic acid Chemical class OC(=O)CCN(CCC(O)=O)CCN(CCC(O)=O)CCC(O)=O KWYJDIUEHHCHCZ-UHFFFAOYSA-N 0.000 description 1
QWZHDKGQKYEBKK-UHFFFAOYSA-N 3-aminochromen-2-one Chemical compound C1=CC=C2OC(=O)C(N)=CC2=C1 QWZHDKGQKYEBKK-UHFFFAOYSA-N 0.000 description 1
CDWQJRGVYJQAIT-UHFFFAOYSA-N 3-benzoylpiperidin-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCNC1=O CDWQJRGVYJQAIT-UHFFFAOYSA-N 0.000 description 1
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
VFIUQNHHBQTNNM-UHFFFAOYSA-N 3-decanoylazepan-2-one Chemical compound CCCCCCCCCC(=O)C1CCCCNC1=O VFIUQNHHBQTNNM-UHFFFAOYSA-N 0.000 description 1
OLDXODLIOAKDPY-UHFFFAOYSA-N 3-decanoylpiperidin-2-one Chemical compound CCCCCCCCCC(=O)C1CCCNC1=O OLDXODLIOAKDPY-UHFFFAOYSA-N 0.000 description 1
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
CLSGAPMZXLVENM-UHFFFAOYSA-N 3-nonanoylazepan-2-one Chemical compound CCCCCCCCC(=O)C1CCCCNC1=O CLSGAPMZXLVENM-UHFFFAOYSA-N 0.000 description 1
WVILLSKUJNGUKA-UHFFFAOYSA-N 3-nonanoylpiperidin-2-one Chemical compound CCCCCCCCC(=O)C1CCCNC1=O WVILLSKUJNGUKA-UHFFFAOYSA-N 0.000 description 1
PUEBLFAPKBDUKE-UHFFFAOYSA-N 3-octanoylazepan-2-one Chemical compound CCCCCCCC(=O)C1CCCCNC1=O PUEBLFAPKBDUKE-UHFFFAOYSA-N 0.000 description 1
YILDPURCUKWQHU-UHFFFAOYSA-N 3-octanoylpiperidin-2-one Chemical compound CCCCCCCC(=O)C1CCCNC1=O YILDPURCUKWQHU-UHFFFAOYSA-N 0.000 description 1
JGKJMBOJWVAMIJ-UHFFFAOYSA-N 4-(2-hydroxypropan-2-yl)-1-methylcyclohexan-1-ol;hydrate Chemical compound O.CC(C)(O)C1CCC(C)(O)CC1 JGKJMBOJWVAMIJ-UHFFFAOYSA-N 0.000 description 1
XGIPGWJHNHEEAL-UHFFFAOYSA-N 4-hexadecoxy-4-oxobutanoic acid Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCC(O)=O XGIPGWJHNHEEAL-UHFFFAOYSA-N 0.000 description 1
CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 1
LSWKXNPXIJXDHU-UHFFFAOYSA-N 4-oxo-4-tetradecoxybutanoic acid Chemical compound CCCCCCCCCCCCCCOC(=O)CCC(O)=O LSWKXNPXIJXDHU-UHFFFAOYSA-N 0.000 description 1
ANJLMAHUPYCFQY-UHFFFAOYSA-N 4-phenyl-1h-benzimidazole-2-sulfonic acid Chemical class C=12NC(S(=O)(=O)O)=NC2=CC=CC=1C1=CC=CC=C1 ANJLMAHUPYCFQY-UHFFFAOYSA-N 0.000 description 1
OTSUEMWVJBSWIQ-UHFFFAOYSA-N 7-methylheptadecan-1-ol Chemical compound CCCCCCCCCCC(C)CCCCCCO OTSUEMWVJBSWIQ-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
235000007173 Abies balsamea Nutrition 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
241000607534 Aeromonas Species 0.000 description 1
102000007698 Alcohol dehydrogenase Human genes 0.000 description 1
108010021809 Alcohol dehydrogenase Proteins 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
240000006439 Aspergillus oryzae Species 0.000 description 1
235000002247 Aspergillus oryzae Nutrition 0.000 description 1
241000750142 Auricula Species 0.000 description 1
244000063299 Bacillus subtilis Species 0.000 description 1
239000004857 Balsam Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
235000003717 Boswellia sacra Nutrition 0.000 description 1
240000007551 Boswellia serrata Species 0.000 description 1
235000012035 Boswellia serrata Nutrition 0.000 description 1
108010073997 Bromide peroxidase Proteins 0.000 description 1
QDWXBVYRECADHW-UHFFFAOYSA-N CNCC(=O)O.C(C(=O)O)(=O)O Chemical compound CNCC(=O)O.C(C(=O)O)(=O)O QDWXBVYRECADHW-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
101100201832 Caenorhabditis elegans rsp-5 gene Proteins 0.000 description 1
101100201838 Caenorhabditis elegans rsp-6 gene Proteins 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
229930192694 Caryophyllenol Natural products 0.000 description 1
108010035722 Chloride peroxidase Proteins 0.000 description 1
RKWGIWYCVPQPMF-UHFFFAOYSA-N Chloropropamide Chemical compound CCCNC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 RKWGIWYCVPQPMF-UHFFFAOYSA-N 0.000 description 1
XXAXVMUWHZHZMJ-UHFFFAOYSA-N Chymopapain Chemical compound OC1=CC(S(O)(=O)=O)=CC(S(O)(=O)=O)=C1O XXAXVMUWHZHZMJ-UHFFFAOYSA-N 0.000 description 1
244000018436 Coriandrum sativum Species 0.000 description 1
235000002787 Coriandrum sativum Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
235000014493 Crataegus Nutrition 0.000 description 1
241001092040 Crataegus Species 0.000 description 1
QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
241001459693 Dipterocarpus zeylanicus Species 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
241000237379 Dolabella Species 0.000 description 1
101000925662 Enterobacteria phage PRD1 Endolysin Proteins 0.000 description 1
239000004863 Frankincense Substances 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
230000005526 G1 to G0 transition Effects 0.000 description 1
240000004859 Gamochaeta purpurea Species 0.000 description 1
239000005792 Geraniol Substances 0.000 description 1
241000245654 Gladiolus Species 0.000 description 1
XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
244000153234 Hibiscus abelmoschus Species 0.000 description 1
108010001336 Horseradish Peroxidase Proteins 0.000 description 1
241001480714 Humicola insolens Species 0.000 description 1
244000018716 Impatiens biflora Species 0.000 description 1
QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
235000019501 Lemon oil Nutrition 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
229920003091 Methocel™ Polymers 0.000 description 1
RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
241000237852 Mollusca Species 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
IFVNATVJZVXOFC-UHFFFAOYSA-N OC(CCC(O)=O)=O.OC(CCC(O)=O)=O.O.O Chemical compound OC(CCC(O)=O)=O.OC(CCC(O)=O)=O.O.O IFVNATVJZVXOFC-UHFFFAOYSA-N 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000019502 Orange oil Nutrition 0.000 description 1
239000004435 Oxo alcohol Substances 0.000 description 1
229910020667 PBr3 Inorganic materials 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
235000003283 Pachira macrocarpa Nutrition 0.000 description 1
240000002834 Paulownia tomentosa Species 0.000 description 1
235000010678 Paulownia tomentosa Nutrition 0.000 description 1
240000002505 Pogostemon cablin Species 0.000 description 1
235000011751 Pogostemon cablin Nutrition 0.000 description 1
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
229920002556 Polyethylene Glycol 300 Polymers 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
108010020346 Polyglutamic Acid Proteins 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
235000006894 Primula auricula Nutrition 0.000 description 1
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical class CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
101710180012 Protease 7 Proteins 0.000 description 1
101000968491 Pseudomonas sp. (strain 109) Triacylglycerol lipase Proteins 0.000 description 1
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
241000220317 Rosa Species 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical group [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 1
229920002359 Tetronic® Polymers 0.000 description 1
240000001085 Trapa natans Species 0.000 description 1
235000014364 Trapa natans Nutrition 0.000 description 1
241001625808 Trona Species 0.000 description 1
238000002441 X-ray diffraction Methods 0.000 description 1
GWBWGPRZOYDADH-UHFFFAOYSA-N [C].[Na] Chemical compound [C].[Na] GWBWGPRZOYDADH-UHFFFAOYSA-N 0.000 description 1
NIPHSGLPJXBULI-UHFFFAOYSA-N [Ca].[Mn].[B].[C] Chemical compound [Ca].[Mn].[B].[C] NIPHSGLPJXBULI-UHFFFAOYSA-N 0.000 description 1
ISWNJSHGUJYCFP-UHFFFAOYSA-N [Ce].[Sr] Chemical compound [Ce].[Sr] ISWNJSHGUJYCFP-UHFFFAOYSA-N 0.000 description 1
YCBJTJZWBGIEQA-UHFFFAOYSA-N [Mn].[Ca].[C].[S] Chemical compound [Mn].[Ca].[C].[S] YCBJTJZWBGIEQA-UHFFFAOYSA-N 0.000 description 1
IPZLLSGGQARVMU-UHFFFAOYSA-N [Na].[Na].C=1(C(=CC=CC1)S(=O)(=O)O)C=CC=1C(=CC=CC1)S(=O)(=O)O Chemical compound [Na].[Na].C=1(C(=CC=CC1)S(=O)(=O)O)C=CC=1C(=CC=CC1)S(=O)(=O)O IPZLLSGGQARVMU-UHFFFAOYSA-N 0.000 description 1
RLLKTVWPIIFQLC-UHFFFAOYSA-N [Sr].[Y].[C] Chemical compound [Sr].[Y].[C] RLLKTVWPIIFQLC-UHFFFAOYSA-N 0.000 description 1
OMAKFDRQPDXBEP-UHFFFAOYSA-N [Y].[Ba].[C] Chemical compound [Y].[Ba].[C] OMAKFDRQPDXBEP-UHFFFAOYSA-N 0.000 description 1
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
QTONSPKDOKVNBJ-UHFFFAOYSA-N acetic acid;n'-(2-aminoethyl)ethane-1,2-diamine Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCNCCN QTONSPKDOKVNBJ-UHFFFAOYSA-N 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229920006243 acrylic copolymer Polymers 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000011149 active material Substances 0.000 description 1
210000000577 adipose tissue Anatomy 0.000 description 1
229960003767 alanine Drugs 0.000 description 1
150000001334 alicyclic compounds Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
125000005599 alkyl carboxylate group Chemical group 0.000 description 1
229920013820 alkyl cellulose Polymers 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
125000005227 alkyl sulfonate group Chemical group 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
125000001118 alkylidene group Chemical group 0.000 description 1
HMKKIXGYKWDQSV-KAMYIIQDSA-N alpha-Amylcinnamaldehyde Chemical compound CCCCC\C(C=O)=C\C1=CC=CC=C1 HMKKIXGYKWDQSV-KAMYIIQDSA-N 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 description 1
125000000539 amino acid group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
229940025131 amylases Drugs 0.000 description 1
230000003625 amylolytic effect Effects 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000003125 aqueous solvent Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
230000003796 beauty Effects 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
150000005130 benzoxazines Chemical class 0.000 description 1
229910052790 beryllium Inorganic materials 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
210000000081 body of the sternum Anatomy 0.000 description 1
238000009835 boiling Methods 0.000 description 1
ZWHAKCCXSBUXPA-UHFFFAOYSA-N boric acid butane Chemical compound B(O)(O)O.CCCC ZWHAKCCXSBUXPA-UHFFFAOYSA-N 0.000 description 1
150000001638 boron Chemical class 0.000 description 1
ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
238000005282 brightening Methods 0.000 description 1
230000003139 buffering effect Effects 0.000 description 1
VABKUVUDFCFASQ-UHFFFAOYSA-N butan-2-one;phenol Chemical compound CCC(C)=O.OC1=CC=CC=C1 VABKUVUDFCFASQ-UHFFFAOYSA-N 0.000 description 1
235000019437 butane-1,3-diol Nutrition 0.000 description 1
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
OLOZVPHKXALCRI-UHFFFAOYSA-L calcium malate Chemical compound [Ca+2].[O-]C(=O)C(O)CC([O-])=O OLOZVPHKXALCRI-UHFFFAOYSA-L 0.000 description 1
239000001362 calcium malate Substances 0.000 description 1
229940016114 calcium malate Drugs 0.000 description 1
235000011038 calcium malates Nutrition 0.000 description 1
HDRTWMBOUSPQON-ODZAUARKSA-L calcium;(z)-but-2-enedioate Chemical compound [Ca+2].[O-]C(=O)\C=C/C([O-])=O HDRTWMBOUSPQON-ODZAUARKSA-L 0.000 description 1
JOSBBXXRYZZWLI-UHFFFAOYSA-L calcium;potassium;carbonate Chemical compound [K+].[Ca+2].[O-]C([O-])=O JOSBBXXRYZZWLI-UHFFFAOYSA-L 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
230000006315 carbonylation Effects 0.000 description 1
238000005810 carbonylation reaction Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001733 carboxylic acid esters Chemical group 0.000 description 1
239000011111 cardboard Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
229920006317 cationic polymer Polymers 0.000 description 1
239000002752 cationic softener Substances 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
239000003518 caustics Substances 0.000 description 1
YZQOWXDLAGPZOW-UHFFFAOYSA-N cerium sodium Chemical compound [Na].[Ce] YZQOWXDLAGPZOW-UHFFFAOYSA-N 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
238000001311 chemical methods and process Methods 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
230000000718 cholinopositive effect Effects 0.000 description 1
ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
229940018557 citraconic acid Drugs 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
229910001603 clinoptilolite Inorganic materials 0.000 description 1
239000003245 coal Substances 0.000 description 1
238000004581 coalescence Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000009508 confectionery Nutrition 0.000 description 1
238000010276 construction Methods 0.000 description 1
AFYCEAFSNDLKSX-UHFFFAOYSA-N coumarin 460 Chemical compound CC1=CC(=O)OC2=CC(N(CC)CC)=CC=C21 AFYCEAFSNDLKSX-UHFFFAOYSA-N 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
GCFAUZGWPDYAJN-UHFFFAOYSA-N cyclohexyl 3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1C=CC(=O)OC1CCCCC1 GCFAUZGWPDYAJN-UHFFFAOYSA-N 0.000 description 1
229960002887 deanol Drugs 0.000 description 1
238000005202 decontamination Methods 0.000 description 1
230000003588 decontaminative effect Effects 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000006356 dehydrogenation reaction Methods 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
IKJFYINYNJYDTA-UHFFFAOYSA-N dibenzothiophene sulfone Chemical compound C1=CC=C2S(=O)(=O)C3=CC=CC=C3C2=C1 IKJFYINYNJYDTA-UHFFFAOYSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
150000004683 dihydrates Chemical class 0.000 description 1
FSBVERYRVPGNGG-UHFFFAOYSA-N dimagnesium dioxido-bis[[oxido(oxo)silyl]oxy]silane hydrate Chemical compound O.[Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O FSBVERYRVPGNGG-UHFFFAOYSA-N 0.000 description 1
XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical class [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
229940042399 direct acting antivirals protease inhibitors Drugs 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
UECLGBSKMMIIPM-UHFFFAOYSA-L disodium 2-[[4-anilino-6-[2-hydroxyethyl(methyl)amino]-1,3,5-triazin-2-yl]amino]-6-[2-(2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].N(C1=CC=CC=C1)C1=NC(=NC(=N1)N(C)CCO)NC1=C(C(=CC=C1)C=CC=1C(=CC=CC=1)S(=O)(=O)[O-])S(=O)(=O)[O-] UECLGBSKMMIIPM-UHFFFAOYSA-L 0.000 description 1
PMPJQLCPEQFEJW-GNTLFSRWSA-L disodium;2-[(z)-2-[4-[4-[(z)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1\C=C/C1=CC=C(C=2C=CC(\C=C/C=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-GNTLFSRWSA-L 0.000 description 1
JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 description 1
YJHDFAAFYNRKQE-YHPRVSEPSA-L disodium;5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S([O-])(=O)=O)=CC=2)S([O-])(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 YJHDFAAFYNRKQE-YHPRVSEPSA-L 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
JHUXOSATQXGREM-UHFFFAOYSA-N dodecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCC(=O)OO JHUXOSATQXGREM-UHFFFAOYSA-N 0.000 description 1
DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 1
229940009662 edetate Drugs 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
HCPOCMMGKBZWSJ-UHFFFAOYSA-N ethyl 3-hydrazinyl-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)NN HCPOCMMGKBZWSJ-UHFFFAOYSA-N 0.000 description 1
CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 1
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
229940043259 farnesol Drugs 0.000 description 1
229930002886 farnesol Natural products 0.000 description 1
238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 1
125000000373 fatty alcohol group Chemical group 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
125000001924 fatty-acyl group Chemical group 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
125000002519 galactosyl group Chemical group C1([C@H](O)[C@@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 description 1
150000008195 galaktosides Chemical class 0.000 description 1
IFYYFLINQYPWGJ-VIFPVBQESA-N gamma-Decalactone Natural products CCCCCC[C@H]1CCC(=O)O1 IFYYFLINQYPWGJ-VIFPVBQESA-N 0.000 description 1
238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
230000009036 growth inhibition Effects 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
210000000514 hepatopancreas Anatomy 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
FDVKPDVESAUTEE-UHFFFAOYSA-N hexane-1,6-diol;2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O.OCCCCCCO FDVKPDVESAUTEE-UHFFFAOYSA-N 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
JISVIRFOSOKJIU-UHFFFAOYSA-N hexylidene Chemical group [CH2+]CCCC[CH-] JISVIRFOSOKJIU-UHFFFAOYSA-N 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000009776 industrial production Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
229910017053 inorganic salt Inorganic materials 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
238000001038 ionspray mass spectrometry Methods 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
108010011519 keratan-sulfate endo-1,4-beta-galactosidase Proteins 0.000 description 1
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical class CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
238000003475 lamination Methods 0.000 description 1
125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010501 lemon oil Substances 0.000 description 1
239000003446 ligand Substances 0.000 description 1
229930007744 linalool Natural products 0.000 description 1
230000002366 lipolytic effect Effects 0.000 description 1
229910003002 lithium salt Inorganic materials 0.000 description 1
159000000002 lithium salts Chemical class 0.000 description 1
229920001427 mPEG Polymers 0.000 description 1
229910001629 magnesium chloride Inorganic materials 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
FBDWCTWJJMORIU-UHFFFAOYSA-N magnesium;hexahydrate Chemical compound O.O.O.O.O.O.[Mg] FBDWCTWJJMORIU-UHFFFAOYSA-N 0.000 description 1
229940049920 malate Drugs 0.000 description 1
BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
238000013507 mapping Methods 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
108010003855 mesentericopeptidase Proteins 0.000 description 1
LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
229940017219 methyl propionate Drugs 0.000 description 1
HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000000479 mixture part Substances 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
125000001419 myristoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
ONLRKTIYOMZEJM-UHFFFAOYSA-N n-methylmethanamine oxide Chemical compound C[NH+](C)[O-] ONLRKTIYOMZEJM-UHFFFAOYSA-N 0.000 description 1
239000003345 natural gas Substances 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
YUPOCHDBBHTUBJ-UHFFFAOYSA-N nonadecan-10-one Chemical compound CCCCCCCCCC(=O)CCCCCCCCC YUPOCHDBBHTUBJ-UHFFFAOYSA-N 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004533 oil dispersion Substances 0.000 description 1
239000002674 ointment Substances 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
239000011368 organic material Substances 0.000 description 1
JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 1
239000006174 pH buffer Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
229960003330 pentetic acid Drugs 0.000 description 1
239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
238000001935 peptisation Methods 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000012169 petroleum derived wax Substances 0.000 description 1
235000019381 petroleum wax Nutrition 0.000 description 1
229960003742 phenol Drugs 0.000 description 1
229940044652 phenolsulfonate Drugs 0.000 description 1
229940100595 phenylacetaldehyde Drugs 0.000 description 1
HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 1
229940067107 phenylethyl alcohol Drugs 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
IPNPIHIZVLFAFP-UHFFFAOYSA-N phosphorus tribromide Chemical compound BrP(Br)Br IPNPIHIZVLFAFP-UHFFFAOYSA-N 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000011297 pine tar Substances 0.000 description 1
229940068124 pine tar Drugs 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920002643 polyglutamic acid Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001444 polymaleic acid Polymers 0.000 description 1
229940045916 polymetaphosphate Drugs 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
239000011164 primary particle Substances 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical class CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
CIBMHJPPKCXONB-UHFFFAOYSA-N propane-2,2-diol Chemical compound CC(C)(O)O CIBMHJPPKCXONB-UHFFFAOYSA-N 0.000 description 1
DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
238000012797 qualification Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000006268 reductive amination reaction Methods 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
235000009165 saligot Nutrition 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
238000007789 sealing Methods 0.000 description 1
150000003335 secondary amines Chemical group 0.000 description 1
210000000582 semen Anatomy 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229940071207 sesquicarbonate Drugs 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
229910001415 sodium ion Chemical group 0.000 description 1
229940001584 sodium metabisulfite Drugs 0.000 description 1
235000010262 sodium metabisulphite Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
239000012418 sodium perborate tetrahydrate Substances 0.000 description 1
PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
229940048842 sodium xylenesulfonate Drugs 0.000 description 1
QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 1
KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
239000011343 solid material Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
235000013555 soy sauce Nutrition 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
YZMCKZRAOLZXAZ-UHFFFAOYSA-N sulfisomidine Chemical compound CC1=NC(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 YZMCKZRAOLZXAZ-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920005613 synthetic organic polymer Polymers 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
238000004885 tandem mass spectrometry Methods 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
150000000000 tetracarboxylic acids Chemical class 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
230000001052 transient effect Effects 0.000 description 1
QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
OHOTVSOGTVKXEL-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]propanoate Chemical class [Na+].[Na+].[Na+].[O-]C(=O)C(C)N(CC([O-])=O)CC([O-])=O OHOTVSOGTVKXEL-UHFFFAOYSA-K 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
210000001364 upper extremity Anatomy 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
235000012141 vanillin Nutrition 0.000 description 1
WXETUDXXEZHSCS-MAVITOTKSA-N vertofix coeur Chemical compound C[C@@H]1CC[C@@]2(C(/CC3)=C\C(C)=O)[C@@H]3C(C)(C)[C@@H]1C2 WXETUDXXEZHSCS-MAVITOTKSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000003232 water-soluble binding agent Substances 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000004804 winding Methods 0.000 description 1
229940032912 zephiran Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

CN97181417A 1996-11-26 1997-11-19 含中链支化伯烷基聚氧化烯表面活性剂的漂白洗涤剂组合物 Expired - Fee Related CN1120226C (zh)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US3191796P	1996-11-26	1996-11-26
US60/031,917		1996-11-26

Related Child Applications (1)

Application Number	Title	Priority Date	Filing Date
CNB021475083A Division CN100457880C (zh)	1996-11-26	1997-11-19	聚氧化烯表面活性剂

Publications (2)

Publication Number	Publication Date
CN1244892A CN1244892A (zh)	2000-02-16
CN1120226C true CN1120226C (zh)	2003-09-03

Family

ID=21862096

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CN97181417A Expired - Fee Related CN1120226C (zh)	1996-11-26	1997-11-19	含中链支化伯烷基聚氧化烯表面活性剂的漂白洗涤剂组合物
CNB021475083A Expired - Fee Related CN100457880C (zh)	1996-11-26	1997-11-19	聚氧化烯表面活性剂

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CNB021475083A Expired - Fee Related CN100457880C (zh)	1996-11-26	1997-11-19	聚氧化烯表面活性剂

Country Status (11)

Country	Link
EP (1)	EP0944699A2 (pt)
JP (2)	JP4364308B2 (pt)
CN (2)	CN1120226C (pt)
AR (1)	AR011769A1 (pt)
BR (1)	BR9713301A (pt)
CA (1)	CA2272139C (pt)
CZ (1)	CZ302716B6 (pt)
HU (1)	HUP0001842A3 (pt)
MA (1)	MA24408A1 (pt)
TR (1)	TR199901159T2 (pt)
WO (1)	WO1998023712A2 (pt)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
MA24136A1 (fr) *	1996-04-16	1997-12-31	Procter & Gamble	Fabrication d'agents de surface .
BR9710430A (pt) *	1996-04-16	1999-08-17	Procter & Gamble	Composi-{es l¡quidas para limpeza contendo tensoativos ramificados selecionados de cadeia m-dia
EG21174A (en) *	1996-04-16	2000-12-31	Procter & Gamble	Surfactant manufacture
PH11997056158B1 (en) *	1996-04-16	2001-10-15	Procter & Gamble	Mid-chain branched primary alkyl sulphates as surfactants
EG22088A (en) *	1996-04-16	2002-07-31	Procter & Gamble	Alkoxylated sulfates
US6093856A (en) *	1996-11-26	2000-07-25	The Procter & Gamble Company	Polyoxyalkylene surfactants
ZA989155B (en)	1997-10-10	1999-04-12	Procter & Gamble	Mixed surfactant system
TR200001729T2 (tr)	1997-10-14	2000-11-21	The Procter & Gamble Company	Zincir ortasından dallanmış yüzeyaktif maddeler içeren granül halinde deterjan terkipleri.
CZ20001350A3 (cs) *	1997-10-14	2001-08-15	The Procter & Gamble Company	Nevodné kapalné detergentní kompozice obsahující rozvětvené povrchově aktivní látky se středními řetězci
ATE288955T1 (de)	1997-10-14	2005-02-15	Procter & Gamble	Flüssige oder gelförmige spülmittelzusammensetzungen enthaltend in der mitte der kette verzweigte tenside
WO1999018928A1 (en)	1997-10-14	1999-04-22	The Procter & Gamble Company	Personal cleansing compositions comprising mid-chain branched surfactants
WO1999064552A1 (en) *	1998-06-10	1999-12-16	The Procter & Gamble Company	Detergent compositions comprising a mannanase and a mid-branched anionic surfactant
US7202205B1 (en)	1999-09-01	2007-04-10	Daniel Stedman Connor	Processes for making surfactants via adsorptive separation and products thereof
EP1241112A3 (en)	2001-03-15	2003-02-26	The Procter & Gamble Company	Flexible multiple compartment pouch
GB0123382D0 (en) *	2001-09-28	2001-11-21	Unilever Plc	Water soluble package and liquid contents thereof
CA2425618C (en) *	2002-04-17	2007-10-23	Nippon Shokubai Co., Ltd.	Specific polymer-compounded detergent composition
DE10326147A1 (de) *	2003-06-06	2005-03-03	Byk-Chemie Gmbh	Epoxid-Addukte und deren Salze als Dispergiermittel
DE102004053969A1 (de) *	2004-11-09	2005-09-15	Clariant Gmbh	Flüssigwaschmittel enthaltend sekundäres Alkansulfonat und kationische Tenside
DE102005040274B3 (de) *	2005-08-24	2007-04-12	Henkel Kgaa	Schaumregulatorgranulat
AU2007269169A1 (en) *	2006-07-03	2008-01-10	Novozymes Biologicals, Inc.	Cleaning composition
JP5334384B2 (ja) *	2007-07-06	2013-11-06	大日本除蟲菊株式会社	アフタードローを抑えたエアゾール用発泡性洗剤組成物
US7994369B2 (en) *	2008-09-22	2011-08-09	The Procter & Gamble Company	Specific polybranched polyaldehydes, polyalcohols, and surfactants, and consumer products based thereon
JP5548390B2 (ja)	2009-05-29	2014-07-16	花王株式会社	液体洗浄剤組成物
ES2643613T3 (es)	2010-08-17	2017-11-23	The Procter & Gamble Company	Detergentes para el lavado de vajillas a mano sostenibles y estables
CN102995468B (zh) *	2012-11-26	2015-04-15	浙江安诺其助剂有限公司	一种涤纶织物染色除油剂及其制备方法
JP6052777B2 (ja) *	2012-12-26	2016-12-27	花王株式会社	液体洗浄剤組成物
JP6207084B2 (ja) *	2014-06-25	2017-10-04	ライオン株式会社	食器洗い用液体洗浄剤
CN107001984B (zh) *	2014-09-08	2019-11-12	宝洁公司	包含支化表面活性剂的洗涤剂组合物
US10017714B2 (en) *	2015-05-19	2018-07-10	Ecolab Usa Inc.	Efficient surfactant system on plastic and all types of ware
US11292002B2 (en)	2016-04-08	2022-04-05	The Governing Council Of The University Of Toronto	Surfactant additives for digital microfluidic devices for high protein content droplets transport
EP3827069A1 (en)	2018-07-25	2021-06-02	Ecolab USA Inc.	Rinse aid formulation for cleaning automotive parts
JP7515518B2 (ja) *	2019-05-10	2024-07-12	ダウグローバルテクノロジーズエルエルシー	界面活性剤ブレンド組成物
CN110452369B (zh) *	2019-07-04	2022-10-28	联泓(江苏)新材料研究院有限公司	一种除油乳化性能优异的异构醇嵌段聚醚及其制备方法和应用
EP3919594A1 (en) *	2020-06-05	2021-12-08	The Procter & Gamble Company	Liquid hand dishwashing detergent composition
EP4426262A1 (en)	2021-11-04	2024-09-11	Coty Inc.	Ethanol-free fragrance chassis
NL2035477B1 (en)	2023-02-20	2024-09-03	Coty Inc	Eye cream formulation
FR3146280A1 (fr)	2023-03-03	2024-09-06	Coty Inc.	Formulations cosmétiques et leurs utilisations
US20240309142A1 (en) *	2023-03-17	2024-09-19	Ecolab Usa Inc.	Capped block copolymers, their synthesis, manufacture, and methods of use
NL2034750B1 (en)	2023-05-02	2024-11-14	Coty Inc	Ethanol-free fragrance chassis

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3887624A (en) *	1972-06-07	1975-06-03	Jefferson Chem Co Inc	Vinylidene alcohol compositions
US4348305A (en) *	1978-04-24	1982-09-07	Henkel Kommanditgesellschaft Auf Aktien	Liquid detergent compositions comprising mixtures of alkyl polyglycol ethers and quaternary ammonium fabric softening agents
WO1994011488A1 (en) *	1992-11-16	1994-05-26	Unilever Plc	Detergent compositions

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2213007A1 (de) *	1972-03-17	1973-09-20	Henkel & Cie Gmbh	Klarspuelmittel fuer die maschinelle geschirreinigung
CA1049046A (en) *	1972-06-07	1979-02-20	Texaco Development Corporation	Vinylidene alcohol compositions
DE2243307C2 (de) *	1972-09-02	1982-04-15	Henkel KGaA, 4000 Düsseldorf	Feste Wasch- und Waschhilfsmittel mit einem Gehalt an vergrauungsverhütenden Zusätzen
CA1059865A (en) *	1974-03-21	1979-08-07	The Procter And Gamble Company	Detergent compositions
GB1495146A (en) *	1974-04-11	1977-12-14	Procter & Gamble	Controlled sudsing detergent compositions
GB1495145A (en) *	1974-04-11	1977-12-14	Procter & Gamble	Controlled sudsing detergent compositions
EP0294574A3 (de) *	1987-06-06	1989-04-26	Degussa Aktiengesellschaft	Wässrige stabile Suspension wasserunlöslicher zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln
TW291496B (pt) *	1991-02-01	1996-11-21	Hoechst Ag
JPH0873890A (ja) *	1994-09-05	1996-03-19	Lion Corp	液体硬表面洗浄剤組成物
CA2207542A1 (en) *	1994-12-16	1996-06-20	Daniel Stedman Connor	Hard surface cleaners comprising highly ethoxylated guerbet alcohols
BR9710430A (pt) *	1996-04-16	1999-08-17	Procter & Gamble	Composi-{es l¡quidas para limpeza contendo tensoativos ramificados selecionados de cadeia m-dia

1997
- 1997-11-19 TR TR1999/01159T patent/TR199901159T2/xx unknown
- 1997-11-19 HU HU0001842A patent/HUP0001842A3/hu unknown
- 1997-11-19 BR BR9713301A patent/BR9713301A/pt not_active IP Right Cessation
- 1997-11-19 CN CN97181417A patent/CN1120226C/zh not_active Expired - Fee Related
- 1997-11-19 CA CA002272139A patent/CA2272139C/en not_active Expired - Fee Related
- 1997-11-19 CN CNB021475083A patent/CN100457880C/zh not_active Expired - Fee Related
- 1997-11-19 EP EP97948391A patent/EP0944699A2/en not_active Withdrawn
- 1997-11-19 JP JP52472898A patent/JP4364308B2/ja not_active Expired - Fee Related
- 1997-11-19 CZ CZ0186899A patent/CZ302716B6/cs not_active IP Right Cessation
- 1997-11-19 WO PCT/US1997/021160 patent/WO1998023712A2/en not_active Application Discontinuation
- 1997-11-25 MA MA24875A patent/MA24408A1/fr unknown
- 1997-11-26 AR ARP970105555A patent/AR011769A1/es unknown
2006
- 2006-09-07 JP JP2006243135A patent/JP2007016246A/ja active Pending

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3887624A (en) *	1972-06-07	1975-06-03	Jefferson Chem Co Inc	Vinylidene alcohol compositions
US4348305A (en) *	1978-04-24	1982-09-07	Henkel Kommanditgesellschaft Auf Aktien	Liquid detergent compositions comprising mixtures of alkyl polyglycol ethers and quaternary ammonium fabric softening agents
WO1994011488A1 (en) *	1992-11-16	1994-05-26	Unilever Plc	Detergent compositions

Also Published As

Publication number	Publication date
CA2272139A1 (en)	1998-06-04
JP4364308B2 (ja)	2009-11-18
CA2272139C (en)	2002-12-17
JP2007016246A (ja)	2007-01-25
CN1244892A (zh)	2000-02-16
EP0944699A2 (en)	1999-09-29
MA24408A1 (fr)	1998-07-01
JP2001506679A (ja)	2001-05-22
AR011769A1 (es)	2000-09-13
WO1998023712A3 (en)	1998-07-23
CZ302716B6 (cs)	2011-09-21
HUP0001842A2 (hu)	2000-09-28
TR199901159T2 (xx)	1999-08-23
WO1998023712A2 (en)	1998-06-04
BR9713301A (pt)	2000-03-21
CN1441042A (zh)	2003-09-10
CZ186899A3 (cs)	2000-04-12
HUP0001842A3 (en)	2001-02-28
CN100457880C (zh)	2009-02-04

Publication	Publication Date	Title
CN1120226C (zh)	2003-09-03	含中链支化伯烷基聚氧化烯表面活性剂的漂白洗涤剂组合物
CN1089367C (zh)	2002-08-21	含中链支化伯烷基硫酸盐的表面活性剂组合物
CN1097089C (zh)	2002-12-25	含中链支化伯烷基烷氧基化硫酸盐的表面活性剂组合物
CN1101461C (zh)	2003-02-12	含中链支化的表面活性剂的洗涤剂组合物
CN1087341C (zh)	2002-07-10	含有选择的中链支化的表面活性剂的洗涤剂组合物
CN1165604C (zh)	2004-09-08	混合表面活性剂体系
CN1281499A (zh)	2001-01-24	含有中链支链表面活性剂的颗粒洗涤剂组合物
CN1168812C (zh)	2004-09-29	洗涤剂组合物
CN1225681A (zh)	1999-08-11	洗涤剂组合物
CN1270620A (zh)	2000-10-18	含有破坏结晶度的表面活性剂混合物的洗涤剂组合物
CN1270622A (zh)	2000-10-18	改良的烷基芳基磺酸盐表面活性剂
JP3308548B2 (ja)	2002-07-29	セルロース誘導体を含む中鎖分岐界面活性剤
CN1281502A (zh)	2001-01-24	含有中链支链表面活性剂的非水液体洗涤剂组合物
CN1276004A (zh)	2000-12-06	中链支化的表面活性剂与纤维素衍生物
CN1239986A (zh)	1999-12-29	含有异肽酶的洗涤剂组合物
CN1228806A (zh)	1999-09-15	含有选择的二阴离子或烷氧基化二阴离子表面活性剂的漂白洗涤剂组合物
CN1276822A (zh)	2000-12-13	中链支化的表面活性剂与钾离子
CN1225122A (zh)	1999-08-04	洗涤剂组合物
CN1225121A (zh)	1999-08-04	洗涤剂组合物
MXPA99003608A (en)	1999-10-14	Detergent compositions containing isopeptidase
CN1225116A (zh)	1999-08-04	洗涤剂组合物

Legal Events

Date	Code	Title	Description
2000-02-16	C06	Publication
2000-02-16	PB01	Publication
2000-02-23	C10	Entry into substantive examination
2000-02-23	SE01	Entry into force of request for substantive examination
2003-07-23	C56	Change in the name or address of the patentee	Owner name: P&G COMPANY Free format text: FORMER NAME OR ADDRESS: THE PROCTER + GAMBLE CO.
2003-07-23	CP01	Change in the name or title of a patent holder	Patentee after: Procter & Gamble Ltd. Patentee before: Procter & Gamble Corp.
2003-09-03	C14	Grant of patent or utility model
2003-09-03	GR01	Patent grant
2014-01-08	C17	Cessation of patent right
2014-01-08	CF01	Termination of patent right due to non-payment of annual fee	Granted publication date: 20030903 Termination date: 20121119