CH684797A5 - Schaumarme Gemische oxalkylierter Amine. - Google Patents

Schaumarme Gemische oxalkylierter Amine. Download PDF

Info

Publication number: CH684797A5
Authority: CH; Switzerland
Prior art keywords: radical; formula; compounds; mixtures; acid
Prior art date: 1992-02-17

Application number

CH450/93A

Other languages

German (de)

English (en)

Inventor

Hans-Peter Dr Baumann

Rene Dr Fricker

Karl-Heinz Weible

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.)

1992-02-17

Filing date

1993-02-15

Publication date

1994-12-30

1993-02-15 Application filed by Sandoz Ag filed Critical Sandoz Ag

1994-12-30 Publication of CH684797A5 publication Critical patent/CH684797A5/de

Links

239000000203 mixture Substances 0.000 title claims description 34
239000006260 foam Substances 0.000 title claims description 30
150000001412 amines Chemical class 0.000 title description 12
238000002360 preparation method Methods 0.000 claims description 46
238000000034 method Methods 0.000 claims description 40
150000001875 compounds Chemical class 0.000 claims description 24
239000003795 chemical substances by application Substances 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 12
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
239000005977 Ethylene Substances 0.000 claims description 10
238000005956 quaternization reaction Methods 0.000 claims description 9
229920001296 polysiloxane Polymers 0.000 claims description 8
239000000654 additive Substances 0.000 claims description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
125000000129 anionic group Chemical group 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
230000005588 protonation Effects 0.000 claims description 6
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 5
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
239000002904 solvent Substances 0.000 claims description 5
125000004122 cyclic group Chemical group 0.000 claims description 4
230000002401 inhibitory effect Effects 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
230000000996 additive effect Effects 0.000 claims description 2
125000002091 cationic group Chemical group 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims 1
239000000047 product Substances 0.000 description 34
238000004043 dyeing Methods 0.000 description 22
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 20
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238000006243 chemical reaction Methods 0.000 description 17
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-1 cerotyi Chemical group 0.000 description 16
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 15
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238000007792 addition Methods 0.000 description 13
230000015572 biosynthetic process Effects 0.000 description 12
230000000694 effects Effects 0.000 description 12
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 11
235000014113 dietary fatty acids Nutrition 0.000 description 11
239000000975 dye Substances 0.000 description 11
239000000194 fatty acid Substances 0.000 description 11
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OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 10
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 10
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238000005187 foaming Methods 0.000 description 9
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239000002253 acid Substances 0.000 description 7
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239000003760 tallow Substances 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
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WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
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ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
239000004952 Polyamide Substances 0.000 description 5
239000004202 carbamide Substances 0.000 description 5
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
239000000463 material Substances 0.000 description 5
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
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239000004094 surface-active agent Substances 0.000 description 5
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239000002585 base Substances 0.000 description 4
125000002511 behenyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
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 4
DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 4
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
150000008044 alkali metal hydroxides Chemical class 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000004040 coloring Methods 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000004744 fabric Substances 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
239000002657 fibrous material Substances 0.000 description 3
229940055577 oleyl alcohol Drugs 0.000 description 3
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 3
125000001117 oleyl 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])=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 3
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 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 3
KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 2
ZZQCGJSFWKIOBB-UHFFFAOYSA-N 2,3,3-trimethyldecan-2-ol Chemical compound CCCCCCCC(C)(C)C(C)(C)O ZZQCGJSFWKIOBB-UHFFFAOYSA-N 0.000 description 2
SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
235000013162 Cocos nucifera Nutrition 0.000 description 2
244000060011 Cocos nucifera Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
229920002292 Nylon 6 Polymers 0.000 description 2
229920002302 Nylon 6,6 Polymers 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-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
235000011054 acetic acid Nutrition 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
229910052921 ammonium sulfate Inorganic materials 0.000 description 2
235000011130 ammonium sulphate Nutrition 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
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239000007859 condensation product Substances 0.000 description 2
239000000835 fiber Substances 0.000 description 2
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125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000011068 loading method Methods 0.000 description 2
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FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
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125000003118 aryl group Chemical group 0.000 description 1
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229910052799 carbon Inorganic materials 0.000 description 1
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150000001768 cations Chemical class 0.000 description 1
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239000007795 chemical reaction product Substances 0.000 description 1
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VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
VVIVVAIHOWVTHB-UHFFFAOYSA-L disodium;3-[[4-amino-9,10-dioxo-3-[2-sulfonato-4-(2,4,4-trimethylpentan-2-yl)phenoxy]anthracen-1-yl]amino]-2,4,6-trimethylbenzenesulfonate Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1NC1=CC(OC=2C(=CC(=CC=2)C(C)(C)CC(C)(C)C)S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O VVIVVAIHOWVTHB-UHFFFAOYSA-L 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
VPNOHCYAOXWMAR-UHFFFAOYSA-N docosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCN VPNOHCYAOXWMAR-UHFFFAOYSA-N 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
238000001035 drying Methods 0.000 description 1
125000004016 elaidoyl 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])=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
239000003995 emulsifying agent Substances 0.000 description 1
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
235000019387 fatty acid methyl ester Nutrition 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
235000021588 free fatty acids Nutrition 0.000 description 1
125000000644 gadoleoyl 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])=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])[H] 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
150000002431 hydrogen Chemical group 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000009981 jet dyeing Methods 0.000 description 1
238000009940 knitting Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 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
125000000403 lignoceroyl 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])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
125000002463 lignoceryl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005644 linolenyl group Chemical group 0.000 description 1
125000002669 linoleoyl 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])=C([H])\C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005645 linoleyl group Chemical group 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
239000002609 medium Substances 0.000 description 1
239000000434 metal complex dye Substances 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 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
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000005830 nonesterified fatty acids Chemical class 0.000 description 1
239000004745 nonwoven fabric Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
125000002811 oleoyl 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])=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
235000006408 oxalic acid Nutrition 0.000 description 1
239000002540 palm oil 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
235000011837 pasties Nutrition 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
125000002270 phosphoric acid ester group Chemical group 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
238000005554 pickling Methods 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920000137 polyphosphoric acid Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
235000021003 saturated fats Nutrition 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
AXMCIYLNKNGNOT-UHFFFAOYSA-N sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-N 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000003696 stearoyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000988 sulfur dye Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
235000021081 unsaturated fats Nutrition 0.000 description 1
239000000984 vat dye Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/24—Polyamides; Polyurethanes
- D06P3/241—Polyamides; Polyurethanes using acid dyes
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2618—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen
- C08G65/2621—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups
- C08G65/2624—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups containing aliphatic amine groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/02—Polyamines
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D06L4/614—Optical bleaching or brightening in aqueous solvents
- D06L4/621—Optical bleaching or brightening in aqueous solvents with anionic brighteners
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
- D06P1/607—Nitrogen-containing polyethers or their quaternary derivatives
- D06P1/6076—Nitrogen-containing polyethers or their quaternary derivatives addition products of amines and alkylene oxides or oxiranes

Landscapes

Chemical & Material Sciences (AREA)
Textile Engineering (AREA)
Engineering & Computer Science (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Coloring (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Detergent Compositions (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

CH450/93A 1992-02-17 1993-02-15 Schaumarme Gemische oxalkylierter Amine. CH684797A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE4204663		1992-02-17

Publications (1)

Publication Number	Publication Date
CH684797A5 true CH684797A5 (de)	1994-12-30

Family

ID=6451872

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH450/93A CH684797A5 (de)	1992-02-17	1993-02-15	Schaumarme Gemische oxalkylierter Amine.

Country Status (8)

Country	Link
JP (1)	JPH0649002A (fr)
KR (1)	KR930018094A (fr)
BE (1)	BE1006384A3 (fr)
CA (1)	CA2089590A1 (fr)
CH (1)	CH684797A5 (fr)
FR (1)	FR2687397A1 (fr)
GB (1)	GB2264500B (fr)
IT (1)	IT1261182B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4312972A1 (de) *	1993-04-21	1994-10-27	Basf Ag	Verwendung von alkoxylierten Polyaminen und deren N--Oxiden als Hilfsmittel für die Lederfärbung
JP5651379B2 (ja) *	2010-06-02	2015-01-14	花王株式会社	水拡散促進能を付与する木綿布の処理方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE552957A (fr) *	1955-11-28
CH478951A (de) *	1967-07-07	1969-06-13	Ciba Geigy	Verfahren zum Färben von Wolle mit 1:2-Metallkompexfarbstoffen
DE2304548A1 (de) *	1973-01-31	1974-08-01	Bayer Ag	Farbstoffpraeparate
DD129922B1 (de) *	1976-10-25	1979-11-28	Hans Clemens	Verfahren zur herstellung permanent antielektrostatischer polyamidfaserstoffe mit hervorragender verarbeitbarkeit
CA1031675A (fr) *	1978-03-06	1978-05-23	Guy Readman	Compositions pour enlever la rouille et proteger la surface des metaux
JPS5721301A (en) *	1980-07-15	1982-02-04	Katayama Chem Works Co Ltd	Agent for controlling sedentary marine life
CH651581A5 (de) *	1981-03-10	1985-09-30	Ciba Geigy Ag	Waessrige zusammensetzungen enthaltend polymere auf acrylsaeurebasis, sowie verfahren zu deren herstellung.
US4444563A (en) *	1981-09-07	1984-04-24	Ciba-Geigy Corporation	Dyeing assistant and use thereof in dyeing or printing synthetic polyamide fibre materials
US4525170A (en) *	1982-05-27	1985-06-25	Ciba-Geigy Corporation	Solid formulations of metal complex dyes
EP0112593B1 (fr) *	1982-12-23	1989-07-19	THE PROCTER & GAMBLE COMPANY	Compositions détergentes contenant des amines éthoxylées ayant des propriétés pour enlever des taches et la contre-redéposition
DE3415880A1 (de) *	1984-04-28	1985-10-31	Henkel KGaA, 4000 Düsseldorf	Waschzusatz
DE3501521A1 (de) *	1985-01-18	1986-07-24	Henkel KGaA, 4000 Düsseldorf	Waessriges konzentriertes textilweichmachungsmittel
US4713482A (en) *	1985-03-26	1987-12-15	Ciba-Geigy Corporation	Maleic or phthalic acid half esters of alkoxylated fatty amines

1993
- 1993-02-12 BE BE9300136A patent/BE1006384A3/fr not_active IP Right Cessation
- 1993-02-12 FR FR9301701A patent/FR2687397A1/fr active Pending
- 1993-02-15 CH CH450/93A patent/CH684797A5/de not_active IP Right Cessation
- 1993-02-15 JP JP5025464A patent/JPH0649002A/ja active Pending
- 1993-02-16 KR KR1019930002136A patent/KR930018094A/ko not_active Withdrawn
- 1993-02-16 GB GB9303074A patent/GB2264500B/en not_active Expired - Fee Related
- 1993-02-16 IT ITRM930085A patent/IT1261182B/it active IP Right Grant
- 1993-02-16 CA CA002089590A patent/CA2089590A1/fr not_active Abandoned

Also Published As

Publication number	Publication date
ITRM930085A1 (it)	1994-08-16
ITRM930085A0 (it)	1993-02-16
JPH0649002A (ja)	1994-02-22
FR2687397A1 (fr)	1993-08-20
IT1261182B (it)	1996-05-09
GB9303074D0 (en)	1993-03-31
GB2264500B (en)	1995-09-27
CA2089590A1 (fr)	1993-08-18
KR930018094A (ko)	1993-09-21
GB2264500A (en)	1993-09-01
BE1006384A3 (fr)	1994-08-09

Legal Events

Date	Code	Title	Description
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE667744C (de)	1938-11-19	Verfahren zur Herstellung von in Wasser loeslichen oder leicht verteilbaren Kondensationsprodukten
DE2625707C3 (de)	1982-04-22	Netz- und Schaumdämpfungsmittel für wäßrige Systeme auf der Basis von anionischen Tensiden und Propylenoxidumsetzungsprodukten
EP0074923B1 (fr)	1985-11-06	Adjuvant de teinture et son utilisation dans la teinture ou l'impression de matériaux en fibres de polyamide synthétique
EP0074335A1 (fr)	1983-03-16	Formulations antimites stables à l'entreposage
DE4332607A1 (de)	1994-03-31	Wäßrige Wachs- und Silicon-Dispersionen, deren Herstellung und Verwendung
DE69900339T2 (de)	2002-07-04	Mittel und Verfahren zur Behandlung von Kunstfasern
US5567400A (en)	1996-10-22	Process for applying a low soiling fiber finish
EP0143077A1 (fr)	1985-05-29	Procédé de teinture de matière textile hydrophobe
DE4433597C2 (de)	1996-10-02	Verfahren zur Erhöhung der Naßgleitfähigkeit von Textilmaterial und Naßgleitmittel dafür
CH684797A5 (de)	1994-12-30	Schaumarme Gemische oxalkylierter Amine.
DE69938079T2 (de)	2009-01-29	Wässrige dispersionen, ihre herstellung und verwendung
DE4303547A1 (en)	1993-08-19	New low foam surfactant mixt. and new modified alkylene oxide copolymer - for use in aq. formulation, esp. as levelling agent in dyeing and optical whitening with anionic cpd.
DE2925477A1 (de)	1981-01-22	Verfahren zum entfernen von oligomerenablagerungen auf textilen materialien
EP0593392B1 (fr)	1996-07-24	Procédé de teinture de fibres polyamides naturelles et synthétiques avec des mélanges de colorants
DE60201572T2 (de)	2005-02-17	Entfettungsmittel für textilfaser, verfahren zu deren herstellung sowie deren verwendung
CH682578A5 (de)	1993-10-15	N-Alkylphthalimidgemisch.
EP0163608A1 (fr)	1985-12-04	Procédé de teinture de matières fibreuses en polyamides naturelles ou synthétiques avec des colorants à complexes métallifères 1:1
DE2802304A1 (de)	1978-07-27	Verfahren zum faerben von wollhaltigem fasermaterial
CH637432A5 (en)	1983-07-29	Dyeing assistant suitable for use in the dyeing of synthetic fibre materials
DE2938606C2 (fr)	1987-11-05
EP1162195B1 (fr)	2006-05-03	Mélanges d' esters d'acide sulfurique
DE19859294A1 (de)	2000-06-29	Textilbehandlungsmittel, Verfahren zu deren Herstellung sowie deren Verwendung
DE2834686C2 (fr)	1988-01-21
DE60022888T2 (de)	2006-07-13	Erhöhung der nassgleitfähigkeit von textilmaterial
EP1347091B1 (fr)	2006-07-19	Adjuvant de teinture