CH681542A5 - - Google Patents

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Info

Publication number: CH681542A5
Authority: CH; Switzerland
Prior art keywords: radical; alkyl; mono; phosphonic acid; phosphine
Prior art date: 1990-08-09

Application number

CH2305/91A

Other languages

German (de)

English (en)

Inventor

Bansi Lal Dr Kaul

Angelos-Elie Dr Vougioukas

Original Assignee

Sandoz Ag

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.)

1990-08-09

Filing date

1991-08-02

Publication date

1993-04-15

1991-08-02 Application filed by Sandoz Ag filed Critical Sandoz Ag

1993-04-15 Publication of CH681542A5 publication Critical patent/CH681542A5/de

Links

150000001875 compounds Chemical class 0.000 claims description 44
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 34
-1 phosphonic acid compound Chemical class 0.000 claims description 18
125000003277 amino group Chemical group 0.000 claims description 17
238000000034 method Methods 0.000 claims description 17
229910000073 phosphorus hydride Inorganic materials 0.000 claims description 17
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
229920003023 plastic Polymers 0.000 claims description 15
239000004033 plastic Substances 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 14
239000001257 hydrogen Substances 0.000 claims description 13
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
150000003009 phosphonic acids Chemical class 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 11
150000001412 amines Chemical class 0.000 claims description 8
229910052801 chlorine Inorganic materials 0.000 claims description 8
239000000460 chlorine Substances 0.000 claims description 8
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 8
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 7
125000002252 acyl group Chemical group 0.000 claims description 7
125000004429 atom Chemical group 0.000 claims description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
229910052794 bromium Inorganic materials 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
150000001408 amides Chemical class 0.000 claims description 4
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
230000003647 oxidation Effects 0.000 claims description 4
238000007254 oxidation reaction Methods 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
150000000000 tetracarboxylic acids Chemical class 0.000 claims description 4
150000003628 tricarboxylic acids Chemical class 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 3
229920000642 polymer Polymers 0.000 claims description 3
230000000087 stabilizing effect Effects 0.000 claims description 3
230000015556 catabolic process Effects 0.000 claims description 2
238000006731 degradation reaction Methods 0.000 claims description 2
IIRVGTWONXBBAW-UHFFFAOYSA-M disodium;dioxido(oxo)phosphanium Chemical compound [Na+].[Na+].[O-][P+]([O-])=O IIRVGTWONXBBAW-UHFFFAOYSA-M 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
239000004753 textile Substances 0.000 claims 3
RXXCIBALSKQCAE-UHFFFAOYSA-N 3-methylbutoxymethylbenzene Chemical compound CC(C)CCOCC1=CC=CC=C1 RXXCIBALSKQCAE-UHFFFAOYSA-N 0.000 claims 1
QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical class OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 12
MLCHBQKMVKNBOV-UHFFFAOYSA-N phenylphosphinic acid Chemical compound OP(=O)C1=CC=CC=C1 MLCHBQKMVKNBOV-UHFFFAOYSA-N 0.000 description 12
239000000047 product Substances 0.000 description 10
239000002253 acid Substances 0.000 description 9
239000000203 mixture Substances 0.000 description 9
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
239000004952 Polyamide Substances 0.000 description 6
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
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 6
229920002647 polyamide Polymers 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000007983 Tris buffer Substances 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
238000009833 condensation Methods 0.000 description 5
230000005494 condensation Effects 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
230000000694 effects Effects 0.000 description 5
QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
OAOBMEMWHJWPNA-UHFFFAOYSA-N (4-aminophenyl)phosphonic acid Chemical compound NC1=CC=C(P(O)(O)=O)C=C1 OAOBMEMWHJWPNA-UHFFFAOYSA-N 0.000 description 4
239000004793 Polystyrene Substances 0.000 description 4
CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 4
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
AKDVWPJLYPAZRM-UHFFFAOYSA-N (4-aminophenyl)phosphinic acid Chemical compound NC1=CC=C(P(O)=O)C=C1 AKDVWPJLYPAZRM-UHFFFAOYSA-N 0.000 description 3
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
229920001155 polypropylene Polymers 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000000985 reactive dye Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
238000005406 washing Methods 0.000 description 3
ZLJGDUKDXZMVLA-UHFFFAOYSA-N 1,2-dihydroacenaphthylen-1-ylphosphonic acid Chemical compound C1=CC(C(P(O)(=O)O)C2)=C3C2=CC=CC3=C1 ZLJGDUKDXZMVLA-UHFFFAOYSA-N 0.000 description 2
QEPXACTUQNGGHW-UHFFFAOYSA-N 2,4,6-trichloro-1h-triazine Chemical compound ClN1NC(Cl)=CC(Cl)=N1 QEPXACTUQNGGHW-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
UTTGAQQFXLNCJP-UHFFFAOYSA-N C1(CC2=CC=CC3=CC=CC1=C23)P(O)=O Chemical compound C1(CC2=CC=CC3=CC=CC1=C23)P(O)=O UTTGAQQFXLNCJP-UHFFFAOYSA-N 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
MWGSSMAHEZDRQP-UHFFFAOYSA-N [hydroxy(phenyl)phosphoryl]oxy-phenylphosphinic acid Chemical compound C=1C=CC=CC=1P(=O)(O)OP(O)(=O)C1=CC=CC=C1 MWGSSMAHEZDRQP-UHFFFAOYSA-N 0.000 description 2
CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 2
HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
238000004061 bleaching Methods 0.000 description 2
238000000071 blow moulding Methods 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000004043 dyeing Methods 0.000 description 2
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000000835 fiber Substances 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
238000001746 injection moulding Methods 0.000 description 2
239000000155 melt Substances 0.000 description 2
YNPFMWCWRVTGKJ-UHFFFAOYSA-N mianserin hydrochloride Chemical compound [H+].[Cl-].C1C2=CC=CC=C2N2CCN(C)CC2C2=CC=CC=C21 YNPFMWCWRVTGKJ-UHFFFAOYSA-N 0.000 description 2
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
229920002239 polyacrylonitrile Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920000915 polyvinyl chloride Polymers 0.000 description 2
125000000714 pyrimidinyl group Chemical group 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 description 1
GVBHCMNXRKOJRH-UHFFFAOYSA-N 2,4,5,6-tetrachloropyrimidine Chemical compound ClC1=NC(Cl)=C(Cl)C(Cl)=N1 GVBHCMNXRKOJRH-UHFFFAOYSA-N 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
239000004801 Chlorinated PVC Substances 0.000 description 1
239000004709 Chlorinated polyethylene Substances 0.000 description 1
239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
238000010640 amide synthesis reaction Methods 0.000 description 1
150000004984 aromatic diamines Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 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
150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
230000000254 damaging effect Effects 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002074 melt spinning Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
YOOYVODKUBZAPO-UHFFFAOYSA-N naphthalen-1-ylphosphonic acid Chemical compound C1=CC=C2C(P(O)(=O)O)=CC=CC2=C1 YOOYVODKUBZAPO-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000005445 natural material Substances 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
CDXVUROVRIFQMV-UHFFFAOYSA-N oxo(diphenoxy)phosphanium Chemical compound C=1C=CC=CC=1O[P+](=O)OC1=CC=CC=C1 CDXVUROVRIFQMV-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920006380 polyphenylene oxide Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000979 synthetic dye Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3834—Aromatic acids (P-C aromatic linkage)
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/48—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
- C07F9/4808—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof the acid moiety containing a substituent or structure which is considered as characteristic
- C07F9/4841—Aromatic acids or derivatives (P-C aromatic linkage)
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6521—Six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Hydrogenated Pyridines (AREA)

CH2305/91A 1990-08-09 1991-08-02 CH681542A5 (sk)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE4025228		1990-08-09

Publications (1)

Publication Number	Publication Date
CH681542A5 true CH681542A5 (sk)	1993-04-15

Family

ID=6411916

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH2305/91A CH681542A5 (sk)	1990-08-09	1991-08-02

Country Status (6)

Country	Link
JP (1)	JPH04253988A (sk)
CH (1)	CH681542A5 (sk)
DE (1)	DE4125440A1 (sk)
FR (1)	FR2666091B1 (sk)
GB (1)	GB2247021B (sk)
IT (1)	IT1253878B (sk)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19751857A1 (de) *	1997-11-22	1999-05-27	Kronos Titan Gmbh	Phosphonatosiloxanbehandelte anorganische Partikel
CN111875584A (zh) *	2020-08-07	2020-11-03	宿迁市振兴化工有限公司	一种多功能光稳定剂的制备方法

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* Cited by examiner, † Cited by third party
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BE611920A (sk) *	1960-12-27
GB1312235A (en) *	1969-03-11	1973-04-04	Glaxo Lab Ltd	Phosphonic acid salts
US3684765A (en) *	1970-01-08	1972-08-15	Sankyo Co	Stabilization of synthetic polymers
SE362441B (sk) *	1970-06-19	1973-12-10	Huels Chemische Werke Ag
GB1372528A (en) *	1970-10-22	1974-10-30	Sandoz Ltd	Benzene phosphonous acid compounds their production and use as stabilizers for organic materials
GB1347009A (en) *	1970-12-15	1974-02-13	Scottish Agricultural Ind Ltd	Plant growth modification
CH557693A (de) *	1971-06-23	1975-01-15	Ciba Geigy Ag	Verfahren zum schuetzen von organischen materialien gegen ultraviolettstrahlung.
US3984501A (en) *	1975-02-03	1976-10-05	Nelson Research & Development Company	Phenyl- and benzylphosphonate esters
DE2602673C3 (de) *	1976-01-24	1979-02-15	Hoechst Ag, 6000 Frankfurt	2,2,6,6-Tetramethyl-4-hydroxy-4carbamoylpiperidin, seine Herstellung und Verwendung
US4366150A (en) *	1979-11-29	1982-12-28	Sumitomo Chemical Company, Limited	Soil disinfectants and method of use
US4452790A (en) *	1982-06-23	1984-06-05	E. R. Squibb & Sons, Inc.	Phosphonyl hydroxyacyl amino acid derivatives as antihypertensives
KR890005170B1 (ko) *	1983-02-01	1989-12-16	롱-쁠랑 아그로시미	유기인 유도체의 염의 제조방법

1991
- 1991-08-01 DE DE4125440A patent/DE4125440A1/de not_active Withdrawn
- 1991-08-02 CH CH2305/91A patent/CH681542A5/de not_active IP Right Cessation
- 1991-08-02 IT ITRM910591A patent/IT1253878B/it active IP Right Grant
- 1991-08-05 GB GB9116822A patent/GB2247021B/en not_active Expired - Fee Related
- 1991-08-08 JP JP3199250A patent/JPH04253988A/ja active Pending
- 1991-08-09 FR FR9110260A patent/FR2666091B1/fr not_active Expired - Fee Related

Also Published As

Publication number	Publication date
GB2247021A (en)	1992-02-19
GB2247021B (en)	1994-11-09
JPH04253988A (ja)	1992-09-09
IT1253878B (it)	1995-08-31
DE4125440A1 (de)	1992-02-13
ITRM910591A1 (it)	1993-02-02
ITRM910591A0 (it)	1991-08-02
FR2666091A1 (fr)	1992-02-28
FR2666091B1 (fr)	1994-01-14
GB9116822D0 (en)	1991-09-18

Publication	Publication Date	Title
DE3920029C2 (de)	1999-05-20	Farbstoffe zum Färben von Kunststoffen
DE69617461T2 (de)	2002-06-27	Cinnamamide und deren verwendung als stabilisatoren
EP0045721A2 (de)	1982-02-10	Piperidylderivate von Triazincopolymeren, Verfahren zu deren Herstellung und solche Derivate enthaltende stabilisierte Zusammensetzung
EP0002261B1 (de)	1982-04-07	Alkylierte 2,2'-Biphenylen-phosphonite und mit deren Hilfe stabilisierte Gemische
DE2615394A1 (de)	1976-10-21	Verfahren zum faerben thermoplastischer kunststoffe in der schmelze
DE602004008228T2 (de)	2008-05-15	Salzartige reaktionsprodukte von hals-derivaten und phosphorhaltigen carbonsäuren zur stabilisierung von polymeren materialien
CH681542A5 (sk)	1993-04-15
DE1544723C3 (de)	1974-11-21	Verfahren zum Herstellen von mit Oxazolverbindungen optisch aufgehellten Formkorpern
EP0003121A1 (de)	1979-07-25	Verwendung von wasserunlöslichen Disazomethinverbindungen zum Färben von thermoplastischen Polyestern in der Masse, insbesondere in der Spinnfärbung
DE3901717A1 (de)	1990-07-26	Synthetische polyamide mit verbesserter anfaerbbarkeit
EP0451228B1 (de)	1994-12-28	Aufheller- und lichtstabilisator-salze
US4384060A (en)	1983-05-17	Colored polyester composition
DE2308572B2 (de)	1978-04-13	Schmelzspinnbare Polyestermassen und deren Verwendung zur Herstellung von Fasern
EP0103193B1 (de)	1985-12-11	Quadratsäureamidderivate, ihre Verwendung als Stabilisierungsmittel sowie die mit diesen behandelten Kunststoffe
DE4408500B4 (de)	2008-07-03	Phosporverbindungen enthaltende polyolefinische Zusammensetzungen
DE3932912A1 (de)	1991-04-11	Sterisch gehinderte aminogruppen enthaltende synthetische polyamide
EP0044424B1 (de)	1984-04-25	Flammfeste Polyamidformmassen und entsprechende Formkörper
DE2850900A1 (de)	1980-06-12	Verwendung von wasserunloeslichen disazomethinverbindungen zum faerben von thermoplastischen polymerisaten und polykondensaten in der masse, die so gefaerbten polymerisate und polykondensate und verfahren zum spinnfaerben
EP1293538B1 (de)	2006-03-29	Verfahren zur Herstellung von Styrylfarbstoffen
WO2024110325A1 (de)	2024-05-30	Gelbe methinfarbstoffe und deren verwendung zum färben von kunststoffen
DE3901716A1 (de)	1990-07-26	Synthetische polyamide mit verbesserter anfaerbbarkeit sowie in der masse gefaerbte synthetische polyamide
DE3930089A1 (de)	1991-03-21	Modifizierte synthetische polyamide
WO2024110327A2 (de)	2024-05-30	Thermostabile methinfarbstoffe
EP1130052A2 (de)	2001-09-05	Verfahren zum Massefärben von Kunststoffen
CH577011A5 (sk)	1976-06-30

Legal Events

Date	Code	Title	Description
1996-04-15	PL	Patent ceased