BE1004777A3 - Melanges de n-alkylphtalimides, compositions les contenant et leur utilisation comme vehiculeurs. - Google Patents

Melanges de n-alkylphtalimides, compositions les contenant et leur utilisation comme vehiculeurs. Download PDF

Info

Publication number: BE1004777A3
Authority: BE; Belgium
Prior art keywords: sep; composition; mixture; weight ratio; phthalimides
Prior art date: 1990-08-27

Application number

BE9100785A

Other languages

English (en)

French (fr)

Original Assignee

Sandoz Sa

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

1991-08-26

Publication date

1993-01-26

1991-08-26 Application filed by Sandoz Sa filed Critical Sandoz Sa

1993-01-26 Application granted granted Critical

1993-01-26 Publication of BE1004777A3 publication Critical patent/BE1004777A3/fr

Links

239000000203 mixture Substances 0.000 title claims abstract description 105
239000000969 carrier Substances 0.000 title claims abstract description 15
230000001804 emulsifying effect Effects 0.000 claims abstract description 7
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims abstract description 5
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 abstract description 3
239000000975 dye Substances 0.000 claims description 36
235000014113 dietary fatty acids Nutrition 0.000 claims description 16
229930195729 fatty acid Natural products 0.000 claims description 16
239000000194 fatty acid Substances 0.000 claims description 16
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 15
238000004043 dyeing Methods 0.000 claims description 15
239000003995 emulsifying agent Substances 0.000 claims description 14
230000003287 optical effect Effects 0.000 claims description 14
150000001875 compounds Chemical class 0.000 claims description 13
150000002148 esters Chemical class 0.000 claims description 11
150000004665 fatty acids Chemical class 0.000 claims description 11
125000005543 phthalimide group Chemical class 0.000 claims description 11
239000004094 surface-active agent Substances 0.000 claims description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
239000006185 dispersion Substances 0.000 claims description 10
239000000758 substrate Substances 0.000 claims description 10
239000000839 emulsion Substances 0.000 claims description 8
150000002430 hydrocarbons Chemical class 0.000 claims description 8
229920001281 polyalkylene Polymers 0.000 claims description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
238000005282 brightening Methods 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
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 5
239000002253 acid Substances 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
239000012874 anionic emulsifier Substances 0.000 claims description 3
239000012875 nonionic emulsifier Substances 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
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239000004215 Carbon black (E152) Substances 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
229930195733 hydrocarbon Natural products 0.000 claims description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
230000005494 condensation Effects 0.000 claims 1
238000009833 condensation Methods 0.000 claims 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 1
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QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
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BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
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125000000129 anionic group Chemical group 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
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
239000007859 condensation product Substances 0.000 description 6
150000002170 ethers Chemical class 0.000 description 6
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HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
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
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
229920000742 Cotton Polymers 0.000 description 4
239000002585 base Substances 0.000 description 4
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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 3
239000004952 Polyamide Substances 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000001166 ammonium sulphate Substances 0.000 description 3
239000002518 antifoaming agent Substances 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
238000009826 distribution Methods 0.000 description 3
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210000002268 wool Anatomy 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
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
150000007513 acids Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
150000001491 aromatic compounds Chemical group 0.000 description 2
239000001045 blue dye Substances 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
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
238000001035 drying Methods 0.000 description 2
150000002191 fatty alcohols Chemical class 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
238000009981 jet dyeing Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
239000011550 stock solution Substances 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
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
JXXOUBHVGURHMH-UHFFFAOYSA-N 2-(4-bromo-3-hydroxyquinolin-2-yl)-3-hydroxyinden-1-one Chemical compound Oc1c(Br)c2ccccc2[nH+]c1C1=C([O-])c2ccccc2C1=O JXXOUBHVGURHMH-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
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 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
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
XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
229920004934 Dacron® Polymers 0.000 description 1
JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 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
239000004698 Polyethylene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
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241001584775 Tunga penetrans Species 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
150000001340 alkali metals 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
230000003254 anti-foaming effect Effects 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
125000004429 atom Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000001049 brown dye Substances 0.000 description 1
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229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
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150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical group 0.000 description 1
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235000019438 castor oil Nutrition 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
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238000001816 cooling Methods 0.000 description 1
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238000007865 diluting Methods 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 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
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230000000694 effects Effects 0.000 description 1
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229910052736 halogen Inorganic materials 0.000 description 1
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239000012535 impurity Substances 0.000 description 1
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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
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AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 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
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
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
235000015927 pasta Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
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229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
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229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000007086 side reaction Methods 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
239000000243 solution Substances 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
238000005507 spraying 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
125000001424 substituent group Chemical group 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
239000000988 sulfur dye Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000004753 textile Substances 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
229960004418 trolamine Drugs 0.000 description 1
239000010981 turquoise Substances 0.000 description 1
RXPRRQLKFXBCSJ-GIVPXCGWSA-N vincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-GIVPXCGWSA-N 0.000 description 1
239000001043 yellow dye 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)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Indole Compounds (AREA)
Cosmetics (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

BE9100785A 1990-08-27 1991-08-26 Melanges de n-alkylphtalimides, compositions les contenant et leur utilisation comme vehiculeurs. BE1004777A3 (fr)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number	Publication Date
BE1004777A3 true BE1004777A3 (fr)	1993-01-26

Family

ID=6413015

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE9100785A BE1004777A3 (fr)	1990-08-27	1991-08-26	Melanges de n-alkylphtalimides, compositions les contenant et leur utilisation comme vehiculeurs.

Country Status (9)

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

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1998038275A1 (en) *	1997-02-28	1998-09-03	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
WO2008097356A2 (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

Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2173311A1 (de) *	1972-02-25	1973-10-05	Hoechst Ag
FR2241654A1 (de) *	1973-08-22	1975-03-21	Bayer Ag
FR2250848A1 (de) *	1973-11-13	1975-06-06	Cassella Farbwerke Mainkur Ag
FR2439224A1 (fr) *	1978-10-19	1980-05-16	Ciba Geigy Ag	Produit auxiliaire de teinturerie et son utilisation dans la teinture de matieres fibreuses synthetiques
GB2112817A (en) *	1981-12-24	1983-07-27	Sandoz Ltd	Improvements in or relating to organic compounds
GB2113257A (en) *	1982-01-02	1983-08-03	Sandoz Ltd	Disperse dyeing textile materials

Family Cites Families (4)

* 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
DE2412427A1 (de) *	1974-03-15	1975-10-16	Bayer Ag	Verfahren zum faerben von natuerlichen und/oder synthetischen polyamidfasermaterialien unterhalb der kochtemperatur
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

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2173311A1 (de) *	1972-02-25	1973-10-05	Hoechst Ag
FR2241654A1 (de) *	1973-08-22	1975-03-21	Bayer Ag
FR2250848A1 (de) *	1973-11-13	1975-06-06	Cassella Farbwerke Mainkur Ag
FR2439224A1 (fr) *	1978-10-19	1980-05-16	Ciba Geigy Ag	Produit auxiliaire de teinturerie et son utilisation dans la teinture de matieres fibreuses synthetiques
GB2112817A (en) *	1981-12-24	1983-07-27	Sandoz Ltd	Improvements in or relating to organic compounds
GB2113257A (en) *	1982-01-02	1983-08-03	Sandoz Ltd	Disperse dyeing textile materials

Also Published As

Publication number	Publication date
FR2666087B1 (fr)	1995-02-03
CH682578A5 (de)	1993-10-15
GB2247470B (en)	1994-07-13
IT1251245B (it)	1995-05-05
JPH04245983A (ja)	1992-09-02
GB9118129D0 (en)	1991-10-09
HK62897A (en)	1997-05-23
GB2247470A (en)	1992-03-04
ES2037597B1 (es)	1994-03-16
CA2049867A1 (en)	1992-02-28
FR2666087A1 (fr)	1992-02-28
ITMI912290A1 (it)	1993-02-27
CA2049867C (en)	2008-04-01
ES2037597A1 (es)	1993-06-16
ITMI912290A0 (it)	1991-08-27

Legal Events

Date	Code	Title	Description
2004-02-29	RE	Patent lapsed	Effective date: 20030831

Publication	Publication Date	Title
US1970578A (en)	1934-08-21	Assistants for the textile and related industries
CH518871A (de)	1972-03-30	Spulenhülse für das Aufwickeln von Garn zur Bildung einer Spule
FR2546543A1 (fr)	1984-11-30	Procede de traitement des textiles
FR2666087A1 (fr)	1992-02-28	Melanges de n-alkylphtalimides, compositions les contenant et leur utilisation comme vehiculeurs.
TW201733971A (zh)	2017-10-01	染色助劑及染色纖維製品之製造方法
BE1009956A3 (fr)	1997-11-04	Procede pour ameliorer le glissement des matieres textiles dans les traitements au mouille, et lubrifiants utilises pour un tel procede.
FR2528459A1 (fr)	1983-12-16	Procede de teinture ou d'impression de textiles encolles
GB343872A (en)	1931-02-09	Improvements in the manufacture and production of wetting, cleansing and dispersing agents
FR2589173A1 (fr)	1987-04-30	Procede de teinture de substrats mixtes
FR2475053A1 (fr)	1981-08-07	Nouvelles compositions a base de lecithine saponifiee, leur preparation et leur application dans l'industrie textile, du cuir et du papier
FR2551474A1 (fr)	1985-03-08	Procede de traitement de matieres textiles cellulosiques
JP2003528988A (ja)	2003-09-30	織物繊維の処理におけるポリアルコキシ化したテルペン誘導体の使用方法
CN109577035B (zh)	2021-12-17	一种纤维染色工艺
BE1004655A3 (fr)	1993-01-05	Procede de teinture des matieres textiles contenant de la cellulose.
BE1006384A3 (fr)	1994-08-09	Nouveaux tensio-actifs faiblement moussants, leur preparation et leur utilisation.
EP0043331B1 (de)	1985-04-03	Verfahren zum Kaltfärben auf Geweben und Produkte zur Durchführung desselben
FR2519356A1 (fr)	1983-07-08	Procede de teinture ou d'impression de substrats textiles avec des colorants de dispersion
BE1004780A3 (fr)	1993-01-26	Nouveaux produits de condensation, leur preparation et leur utilisation comme auxiliaires de teinture.
BE671110A (de)
DE2801742A1 (de)	1978-07-27	Farbstoffzubereitungen saurer und kationischer farbstoffe und faerbeverfahren
FR2611763A1 (fr)	1988-09-09	Procede de teinture de polyamides naturels et/ou synthetiques avec des colorants anioniques
BE1005672A3 (fr)	1993-12-14	Utilisation de composes aromatiques contenant des groupes sulfo, comme auxiliares d'application dans le traitement des matieres fibreuses.
EP0671383B1 (de)	1998-01-07	Wachsartiger Weichmacher für Textilien, Verfahren für seine Herstellung, ihn enthaltende wässrige Zusammensetzungen und seine Verwendung als Textilbehandlungsmittel
FR2488886A1 (fr)	1982-02-26	Procede d'obtention d'un melange d'esters de phenols chloro-substitues, emulsions renfermant ce melange et leur application
FR2611737A1 (fr)	1988-09-09	Melanges de colorants anioniques pour la teinture de la laine