CH682578A5 - N-Alkylphthalimidgemisch. - Google Patents

N-Alkylphthalimidgemisch. Download PDF

Info

Publication number: CH682578A5
Authority: CH; Switzerland
Prior art keywords: preparations; mixture; phthalimide; polyalkylene glycol; mono
Prior art date: 1990-08-27

Application number

CH2486/91A

Other languages

German (de)

English (en)

Inventor

Hans-Peter Dr Baumann

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.)

1990-08-27

Filing date

1991-08-23

Publication date

1993-10-15

1991-08-23 Application filed by Sandoz Ag filed Critical Sandoz Ag

1993-10-15 Publication of CH682578A5 publication Critical patent/CH682578A5/de

Links

238000002360 preparation method Methods 0.000 claims description 50
239000000203 mixture Substances 0.000 claims description 37
229920001521 polyalkylene glycol ether Polymers 0.000 claims description 18
-1 glycerol fatty acid ester Chemical class 0.000 claims description 17
230000001804 emulsifying effect Effects 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 13
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 12
235000014113 dietary fatty acids Nutrition 0.000 claims description 11
239000003995 emulsifying agent Substances 0.000 claims description 11
229930195729 fatty acid Natural products 0.000 claims description 11
239000000194 fatty acid Substances 0.000 claims description 11
229920005862 polyol Polymers 0.000 claims description 11
239000004094 surface-active agent Substances 0.000 claims description 11
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
150000003077 polyols Chemical class 0.000 claims description 10
239000004215 Carbon black (E152) Substances 0.000 claims description 7
229930195733 hydrocarbon Natural products 0.000 claims description 7
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 6
150000002430 hydrocarbons Chemical class 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000005543 phthalimide group Chemical class 0.000 claims description 4
150000003839 salts Chemical group 0.000 claims description 4
239000002253 acid Substances 0.000 claims description 3
125000006530 (C4-C6) alkyl group Chemical group 0.000 claims description 2
RLARUBPTQYKZKA-UHFFFAOYSA-N 2-propylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCC)C(=O)C2=C1 RLARUBPTQYKZKA-UHFFFAOYSA-N 0.000 claims description 2
229910019142 PO4 Inorganic materials 0.000 claims description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
239000013543 active substance Substances 0.000 claims description 2
239000012874 anionic emulsifier Substances 0.000 claims description 2
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 2
LQQCGEGRINLHDP-UHFFFAOYSA-N carboxyphosphoric acid Chemical compound OC(=O)OP(O)(O)=O LQQCGEGRINLHDP-UHFFFAOYSA-N 0.000 claims description 2
239000012875 nonionic emulsifier Substances 0.000 claims description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
239000010452 phosphate Substances 0.000 claims description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
239000000975 dye Substances 0.000 description 26
238000004043 dyeing Methods 0.000 description 18
229920000728 polyester Polymers 0.000 description 14
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
239000004744 fabric Substances 0.000 description 11
239000000047 product Substances 0.000 description 11
239000006185 dispersion Substances 0.000 description 9
150000004665 fatty acids Chemical group 0.000 description 8
239000000835 fiber Substances 0.000 description 8
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
239000000758 substrate Substances 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 6
229910052921 ammonium sulfate Inorganic materials 0.000 description 6
235000011130 ammonium sulphate Nutrition 0.000 description 6
238000007639 printing Methods 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
239000000969 carrier Substances 0.000 description 5
239000002657 fibrous material Substances 0.000 description 5
229920003986 novolac Polymers 0.000 description 5
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 4
229920000742 Cotton Polymers 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
239000000654 additive Substances 0.000 description 4
125000000129 anionic group Chemical group 0.000 description 4
239000002585 base Substances 0.000 description 4
235000019253 formic acid Nutrition 0.000 description 4
230000003287 optical effect Effects 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
210000002268 wool Anatomy 0.000 description 4
239000004952 Polyamide Substances 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002518 antifoaming agent Substances 0.000 description 3
238000005282 brightening Methods 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
150000001875 compounds Chemical class 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000006260 foam Substances 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 3
229920002647 polyamide Polymers 0.000 description 3
238000003860 storage Methods 0.000 description 3
ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical group CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 2
DLKDEVCJRCPTLN-UHFFFAOYSA-N 2-butylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCC)C(=O)C2=C1 DLKDEVCJRCPTLN-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
229920002301 cellulose acetate Polymers 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004040 coloring Methods 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
239000000986 disperse dye Substances 0.000 description 2
238000009826 distribution Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
150000003949 imides Chemical class 0.000 description 2
238000005470 impregnation Methods 0.000 description 2
239000000976 ink Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
235000021313 oleic acid Nutrition 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
239000001044 red dye Substances 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
239000000984 vat dye Substances 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
OXLITIGRBOEDEZ-UHFFFAOYSA-N 1,5-diamino-4,8-dihydroxy-2-(4-hydroxyphenyl)anthracene-9,10-dione Chemical compound C=1C(O)=C2C(=O)C=3C(N)=CC=C(O)C=3C(=O)C2=C(N)C=1C1=CC=C(O)C=C1 OXLITIGRBOEDEZ-UHFFFAOYSA-N 0.000 description 1
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
RHEVAQGXLUQWBM-UHFFFAOYSA-N 2-(1-amino-9,10-dioxoanthracen-2-yl)naphtho[2,3-f][1,3]benzoxazole-5,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2O3)=C1C=C2N=C3C1=C(N)C(C(=O)C2=CC=CC=C2C2=O)=C2C=C1 RHEVAQGXLUQWBM-UHFFFAOYSA-N 0.000 description 1
DVBLPJWQXDCAKU-UHFFFAOYSA-N 2-(4-bromo-3-hydroxyquinolin-2-yl)indene-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C1=C(O)C(Br)=C2C=CC=CC2=N1 DVBLPJWQXDCAKU-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
QEORVDCGZONWCJ-UHFFFAOYSA-N 2-[[4-[2-cyanoethyl(ethyl)amino]phenyl]diazenyl]-5-nitrobenzonitrile Chemical compound C1=CC(N(CCC#N)CC)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1C#N QEORVDCGZONWCJ-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
KYWBKKCQVIZQJV-UHFFFAOYSA-N 2-hexylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCCC)C(=O)C2=C1 KYWBKKCQVIZQJV-UHFFFAOYSA-N 0.000 description 1
SRFRJCMUBGZTAP-UHFFFAOYSA-N 2-pentylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCC)C(=O)C2=C1 SRFRJCMUBGZTAP-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
ZCMWRFQVYXHUQN-UHFFFAOYSA-N 4,11-diamino-1-imino-2-(3-methoxypropyl)naphtho[2,3-f]isoindole-3,5,10-trione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=C(C(N(CCCOC)C1=N)=O)C1=C2N ZCMWRFQVYXHUQN-UHFFFAOYSA-N 0.000 description 1
NZDXSXLYLMHYJA-UHFFFAOYSA-M 4-[(1,3-dimethylimidazol-1-ium-2-yl)diazenyl]-n,n-dimethylaniline;chloride Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1N=NC1=[N+](C)C=CN1C NZDXSXLYLMHYJA-UHFFFAOYSA-M 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
241000251468 Actinopterygii Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
229920004934 Dacron® Polymers 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-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
241000083869 Polyommatus dorylas Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
241001584775 Tunga penetrans Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000001124 arachidoyl 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])[H] 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
ZFNYLMNOLDSXFB-UHFFFAOYSA-N azane dodecyl benzenesulfonate ethanol Chemical group N.CCO.CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 ZFNYLMNOLDSXFB-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
150000001768 cations Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
238000011161 development Methods 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
229940043276 diisopropanolamine Drugs 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
TUXJTJITXCHUEL-UHFFFAOYSA-N disperse red 11 Chemical compound C1=CC=C2C(=O)C3=C(N)C(OC)=CC(N)=C3C(=O)C2=C1 TUXJTJITXCHUEL-UHFFFAOYSA-N 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
235000019387 fatty acid methyl ester Nutrition 0.000 description 1
235000020988 fatty fish Nutrition 0.000 description 1
238000005187 foaming Methods 0.000 description 1
RRDQTXGFURAKDI-UHFFFAOYSA-N formaldehyde;naphthalene-2-sulfonic acid Chemical compound O=C.C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 RRDQTXGFURAKDI-UHFFFAOYSA-N 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 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
229910052744 lithium Inorganic materials 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
VHLFTCNAACYPDY-UHFFFAOYSA-N methyl 3-[n-ethyl-4-[(5-nitro-2,1-benzothiazol-3-yl)diazenyl]anilino]propanoate Chemical compound C1=CC(N(CCC(=O)OC)CC)=CC=C1N=NC1=C2C=C([N+]([O-])=O)C=CC2=NS1 VHLFTCNAACYPDY-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 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
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000004745 nonwoven fabric Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000002889 oleic acids Chemical class 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
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
229920000139 polyethylene terephthalate 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
238000012545 processing Methods 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000010025 steaming 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
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000988 sulfur dye Substances 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000012546 transfer Methods 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
YXZRCLVVNRLPTP-UHFFFAOYSA-J turquoise blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Cu+2].NC1=NC(Cl)=NC(NC=2C=C(NS(=O)(=O)C3=CC=4C(=C5NC=4NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)NC=4NC(=C6C=C(C=CC6=4)S([O-])(=O)=O)NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)N5)C=C3)C(=CC=2)S([O-])(=O)=O)=N1 YXZRCLVVNRLPTP-UHFFFAOYSA-J 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000004804 winding Methods 0.000 description 1
239000002759 woven fabric 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
- 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
- D06P1/64—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 low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6495—Compounds containing carbonamide -RCON= (R=H or hydrocarbons)
- D06P1/6498—Compounds containing -CONCO-, e.g. phthalimides, hydantoine; Compounds containing RCONHSO2R (R=H or hydrocarbon)

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Coloring (AREA)
Indole Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cosmetics (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

CH2486/91A 1990-08-27 1991-08-23 N-Alkylphthalimidgemisch. CH682578A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE4027075		1990-08-27

Publications (1)

Publication Number	Publication Date
CH682578A5 true CH682578A5 (de)	1993-10-15

Family

ID=6413015

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH2486/91A CH682578A5 (de)	1990-08-27	1991-08-23	N-Alkylphthalimidgemisch.

Country Status (9)

Country	Link
JP (1)	JPH04245983A (it)
BE (1)	BE1004777A3 (it)
CA (1)	CA2049867C (it)
CH (1)	CH682578A5 (it)
ES (1)	ES2037597B1 (it)
FR (1)	FR2666087B1 (it)
GB (1)	GB2247470B (it)
HK (1)	HK62897A (it)
IT (1)	IT1251245B (it)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU6537098A (en) *	1997-02-28	1998-09-18	Sybron Chemicals Inc.	Clay-containing textile material treating composition and method
US5972049A (en) *	1998-01-28	1999-10-26	Sybron Chemicals Inc.	Clay-containing dispersing composition for carriers used in the disperse dyeing of hydrophobic textiles
GB0605260D0 (en) *	2006-03-15	2006-04-26	Dylon Internat Ltd	Fabric whitener
CA2661685A1 (en) *	2006-09-08	2008-08-14	Southern Mills, Inc.	Methods and systems for providing dyed, stretchable flame resistant fabrics and garments
CN101498107B (zh) *	2008-07-11	2012-04-25	杭州传化精细化工有限公司	一种修色剂及其制备方法
JP5629104B2 (ja) *	2010-03-24	2014-11-19	株式会社クラレ	ポリエーテルイミド繊維の染色方法及びその染色物

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1769210A1 (de) *	1968-04-20	1970-12-17	Bayer Ag	Druck- und Faerbeverfahren
BE795961A (fr) *	1972-02-25	1973-08-27	Hoechst Ag	Application d'hemi-esters sulfuriques a la dispersion de colorants
DE2342293A1 (de) *	1973-08-22	1975-04-24	Bayer Ag	Druck- und faerbeverfahren
DE2356548A1 (de) *	1973-11-13	1975-06-26	Cassella Farbwerke Mainkur Ag	Verfahren zum faerben von polyamidfasern mit schwefelfarbstoffen
DE2412427A1 (de) *	1974-03-15	1975-10-16	Bayer Ag	Verfahren zum faerben von natuerlichen und/oder synthetischen polyamidfasermaterialien unterhalb der kochtemperatur
US4252534A (en) *	1978-10-19	1981-02-24	Ciba-Geigy Corporation	Dyeing assistants and their use in dyeing synthetic fibre material
GB2112817B (en) *	1981-12-24	1986-01-22	Sandoz Ltd	Improvements in or relating to organic compounds
CH653068A5 (de) *	1982-01-02	1985-12-13	Sandoz Ag	Hilfsmittel fuer das faerben mit dispersionsfarbstoffen.
DE3834737A1 (de) *	1988-10-12	1990-04-19	Bayer Ag	Carrier fuer das faerben von polyestermaterialien
DE3902052A1 (de) *	1989-01-25	1990-07-26	Bayer Ag	Carrier fuer das faerben von hydrophoben fasermaterialien

1991
- 1991-08-21 ES ES9101917A patent/ES2037597B1/es not_active Expired - Fee Related
- 1991-08-22 GB GB9118129A patent/GB2247470B/en not_active Expired - Fee Related
- 1991-08-23 JP JP3212114A patent/JPH04245983A/ja active Pending
- 1991-08-23 CH CH2486/91A patent/CH682578A5/de not_active IP Right Cessation
- 1991-08-26 CA CA002049867A patent/CA2049867C/en not_active Expired - Lifetime
- 1991-08-26 BE BE9100785A patent/BE1004777A3/fr not_active IP Right Cessation
- 1991-08-27 IT ITMI912290A patent/IT1251245B/it active IP Right Grant
- 1991-08-27 FR FR9110710A patent/FR2666087B1/fr not_active Expired - Fee Related
1997
- 1997-05-15 HK HK62897A patent/HK62897A/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
HK62897A (en)	1997-05-23
IT1251245B (it)	1995-05-05
GB2247470B (en)	1994-07-13
CA2049867A1 (en)	1992-02-28
BE1004777A3 (fr)	1993-01-26
ES2037597B1 (es)	1994-03-16
ES2037597A1 (es)	1993-06-16
GB9118129D0 (en)	1991-10-09
GB2247470A (en)	1992-03-04
FR2666087B1 (fr)	1995-02-03
FR2666087A1 (fr)	1992-02-28
ITMI912290A0 (it)	1991-08-27
ITMI912290A1 (it)	1992-02-28
CA2049867C (en)	2008-04-01
JPH04245983A (ja)	1992-09-02

Legal Events

Date	Code	Title	Description
1996-07-15	NV	New agent	Representative=s name: SANDOZ TECHNOLOGIE AG
1996-07-15	PUE	Assignment	Owner name: SANDOZ AG TRANSFER- CLARIANT FINANCE (BVI) LIMITED
1997-03-14	NV	New agent	Representative=s name: CLARIANT INTERNATIONAL LTD.
2010-03-31	PL	Patent ceased

Publication	Publication Date	Title
CH666275A5 (de)	1988-07-15	Acetylerythromycinstearat, verfahren zu dessen herstellung und dieses enthaltende arzneimittel.
EP0204656A1 (de)	1986-12-10	Verfahren zum Färben von hydrophobem Fasermaterial
EP0143077B1 (de)	1988-07-27	Verfahren zum Färben von hydrophobem Fasermaterial
EP0364792A2 (de)	1990-04-25	Carrier für das Färben von Polyestermaterialien
CH682578A5 (de)	1993-10-15	N-Alkylphthalimidgemisch.
DE2941763C2 (it)	1989-01-26
EP0657577A1 (de)	1995-06-14	Verfahren zur photochemischen und thermischen Stabilisierung von ungefärbten und gefärbten oder bedruckten Polyesterfasermaterialien
EP1469121B1 (de)	2005-09-28	Egalisiermittel
DE1469603A1 (de)	1969-08-28	Verfahren zur Trocknung und Fixierung auf Acrylnitrilpolymerisate enthaltendes oder daraus bestehendes Fasergut aufgeklotzter basischer Farbstoffe mit Trockenhitze
DE2758881C2 (de)	1980-03-06	Verfahren zum Färben von natürlichen und/oder synthetische Fasern enthaltenden textlien Materialien
DE4127516A1 (de)	1992-03-05	N-alkylphthalimidgemisch
EP0099111B1 (de)	1986-11-05	Verfahren zum HT-Färben von Polyestermaterialien
DE1904919C2 (de)	1975-11-27	06.11.68 Schweiz 16521-68 Verfahren zum Färben und Bedrucken von Textilmaterial aus hydrophoben Polyestern
CH637432A5 (en)	1983-07-29	Dyeing assistant suitable for use in the dyeing of synthetic fibre materials
DE2215717A1 (de)	1972-10-12	Verfahren zum Farben oder Bedrucken von organischen, synthetischen, hydropho ben Fasern
EP1348800B1 (de)	2004-07-07	Verwendung von Alkylbenzoaten als Egalisiermittel zum Färben von Polyester-Fasermaterialien
DE2512462C2 (de)	1977-05-12	Verfahren zum bedrucken oder klotzfaerben von polyester, cellulose-triacetat, cellulose 2 1/2 acetat und deren mischungen
DE2239930A1 (de)	1973-06-14	Verfahren zur faerbung von polyesterfasern
DE2755295A1 (de)	1978-06-15	Verfahren zum faerben von polyestermaterialien
DE2521106C3 (de)	1977-01-27	Verfahren zum Färben von synthetische Fasern enthaltenden Materialien
CH672274A5 (it)	1989-11-15
DE2506466A1 (de)	1976-08-26	Emulgiermittel fuer faerbebeschleuniger auf basis von alkylnaphthalinen
CH276173A (de)	1951-06-30	Zeichenhilfsgerät.
DE2724644B2 (de)	1980-02-28	Verfahren zum Farben von wollhaltigen Fasermaterialien
DE2432661A1 (de)	1976-01-29	Verfahren zum faerben von synthetischen fasern