BE439230A - - Google Patents

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Publication number

BE439230A

BE439230A BE439230DA BE439230A BE 439230 A BE439230 A BE 439230A BE 439230D A BE439230D A BE 439230DA BE 439230 A BE439230 A BE 439230A

Authority

BE

Belgium

Prior art keywords

weight

parts

solution

ether

hal

Prior art date

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• 239000000047 product Substances 0.000 claims description 16
• VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
• FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 10
• 239000011780 sodium chloride Substances 0.000 claims description 10
• 239000002253 acid Substances 0.000 claims description 8
• 150000001875 compounds Chemical class 0.000 claims description 7
• 230000000875 corresponding Effects 0.000 claims description 6
• 238000000034 method Methods 0.000 claims description 5
• 239000004215 Carbon black (E152) Substances 0.000 claims description 4
• KXDHJXZQYSOELW-UHFFFAOYSA-N carbamate Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 4
• 239000007795 chemical reaction product Substances 0.000 claims description 4
• 239000000706 filtrate Substances 0.000 claims description 4
• 239000007859 condensation product Substances 0.000 claims description 3
• 125000005843 halogen group Chemical group 0.000 claims description 3
• 229910052757 nitrogen Inorganic materials 0.000 claims description 3
• 239000011230 binding agent Substances 0.000 claims description 2
• 125000004432 carbon atoms Chemical group C* 0.000 claims description 2
• 238000001914 filtration Methods 0.000 claims description 2
• 125000005842 heteroatoms Chemical group 0.000 claims description 2
• 229910052739 hydrogen Inorganic materials 0.000 claims description 2
• UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
• 239000001257 hydrogen Substances 0.000 claims description 2
• 125000004433 nitrogen atoms Chemical group N* 0.000 claims description 2
• 230000001034 aminogenic Effects 0.000 claims 1
• 230000003472 neutralizing Effects 0.000 claims 1
• 238000002360 preparation method Methods 0.000 claims 1
• HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
• RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
• YMWUJEATGCHHMB-UHFFFAOYSA-N methylene dichloride Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 22
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
• 239000002904 solvent Substances 0.000 description 10
• -1 salt ethers Chemical class 0.000 description 9
• 235000011121 sodium hydroxide Nutrition 0.000 description 9
• 238000003756 stirring Methods 0.000 description 9
• CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
• CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
• BCUPGIHTCQJCSI-UHFFFAOYSA-N chloromethanol Chemical compound OCCl BCUPGIHTCQJCSI-UHFFFAOYSA-N 0.000 description 7
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
• KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 6
• 238000006243 chemical reaction Methods 0.000 description 6
• 238000004821 distillation Methods 0.000 description 6
• 239000000203 mixture Substances 0.000 description 5
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
• 239000001187 sodium carbonate Substances 0.000 description 4
• 229910000029 sodium carbonate Inorganic materials 0.000 description 4
• 230000001476 alcoholic Effects 0.000 description 3
• 238000001816 cooling Methods 0.000 description 3
• UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
• 229960003237 betaine Drugs 0.000 description 2
• 239000003795 chemical substances by application Substances 0.000 description 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
• 239000006260 foam Substances 0.000 description 2
• CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
• LRZFEBJUJIQVDQ-UHFFFAOYSA-N methyl 2-(dimethylamino)acetate Chemical compound COC(=O)CN(C)C LRZFEBJUJIQVDQ-UHFFFAOYSA-N 0.000 description 2
• REGWVSTWPUXKJS-UHFFFAOYSA-N methyl 2-piperidin-1-ylacetate Chemical compound COC(=O)CN1CCCCC1 REGWVSTWPUXKJS-UHFFFAOYSA-N 0.000 description 2
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
• 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
• 238000007127 saponification reaction Methods 0.000 description 2
• 239000007787 solid Substances 0.000 description 2
• UCKMPCXJQFINFW-UHFFFAOYSA-N sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
• 239000004753 textile Substances 0.000 description 2
• YVSNBDFDMHIXBF-UHFFFAOYSA-N 1-(chloromethylsulfanyl)dodecane Chemical compound CCCCCCCCCCCCSCCl YVSNBDFDMHIXBF-UHFFFAOYSA-N 0.000 description 1
• NMMIRFKUKVHGTQ-UHFFFAOYSA-N 1-butoxydodecane Chemical compound CCCCCCCCCCCCOCCCC NMMIRFKUKVHGTQ-UHFFFAOYSA-N 0.000 description 1
• FVEAPUWITOJHBI-UHFFFAOYSA-N 1-butoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCC FVEAPUWITOJHBI-UHFFFAOYSA-N 0.000 description 1
• CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
• FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 1
• WXZZJKVGEJBSJP-UHFFFAOYSA-M 2-(diethylamino)butanoate Chemical compound CCC(C([O-])=O)N(CC)CC WXZZJKVGEJBSJP-UHFFFAOYSA-M 0.000 description 1
• QCYOIFVBYZNUNW-UHFFFAOYSA-N 2-(dimethylazaniumyl)propanoate Chemical compound CN(C)C(C)C(O)=O QCYOIFVBYZNUNW-UHFFFAOYSA-N 0.000 description 1
• HRQGCQVOJVTVLU-UHFFFAOYSA-N Bis(chloromethyl) ether Chemical class ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
• 210000001736 Capillaries Anatomy 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
• UCFFGYASXIPWPD-UHFFFAOYSA-N Methyl hypochlorite Chemical compound COCl UCFFGYASXIPWPD-UHFFFAOYSA-N 0.000 description 1
• FFDGPVCHZBVARC-UHFFFAOYSA-N N,N-dimethylglycine zwitterion Chemical compound CN(C)CC(O)=O FFDGPVCHZBVARC-UHFFFAOYSA-N 0.000 description 1
• GQRUHVMVWNKUFW-UMQXSMKFSA-N abietadienol Chemical compound OC[C@]1(C)CCC[C@]2(C)[C@@H](CCC(C(C)C)=C3)C3=CCC21 GQRUHVMVWNKUFW-UMQXSMKFSA-N 0.000 description 1
• QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 239000002671 adjuvant Substances 0.000 description 1
• 230000000240 adjuvant Effects 0.000 description 1
• 239000003513 alkali Substances 0.000 description 1
• 150000003863 ammonium salts Chemical class 0.000 description 1
• 238000005282 brightening Methods 0.000 description 1
• OEDMOCYNWLHUDP-UHFFFAOYSA-N bromomethanol Chemical compound OCBr OEDMOCYNWLHUDP-UHFFFAOYSA-N 0.000 description 1
• CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 1
• 239000012459 cleaning agent Substances 0.000 description 1
• 235000014113 dietary fatty acids Nutrition 0.000 description 1
• 239000002270 dispersing agent Substances 0.000 description 1
• 238000004090 dissolution Methods 0.000 description 1
• 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 1
• 230000000694 effects Effects 0.000 description 1
• 150000002170 ethers Chemical class 0.000 description 1
• DJGCAHHIFOEPPU-UHFFFAOYSA-N ethyl 4-(diethylamino)butanoate Chemical compound CCOC(=O)CCCN(CC)CC DJGCAHHIFOEPPU-UHFFFAOYSA-N 0.000 description 1
• 238000001704 evaporation Methods 0.000 description 1
• 239000000194 fatty acid Substances 0.000 description 1
• 150000004665 fatty acids Chemical class 0.000 description 1
• LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
• 125000000623 heterocyclic group Chemical group 0.000 description 1
• 239000003906 humectant Substances 0.000 description 1
• 239000003077 lignite Substances 0.000 description 1
• 239000000395 magnesium oxide Substances 0.000 description 1
• KJSCSZQWNCEXBT-UHFFFAOYSA-N methyl 4-piperidin-1-ylbutanoate Chemical compound COC(=O)CCCN1CCCCC1 KJSCSZQWNCEXBT-UHFFFAOYSA-N 0.000 description 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
• 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 1
• 239000000376 reactant Substances 0.000 description 1
• 239000000344 soap Substances 0.000 description 1
• 150000003568 thioethers Chemical class 0.000 description 1