CH678430A5 - - Google Patents

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Info

Publication number: CH678430A5
Authority: CH; Switzerland
Prior art keywords: formula; dye; hydrogen; parts; dyes
Prior art date: 1989-01-07

Application number

CH20/90A

Other languages

German (de)

English (en)

Inventor

Ulrich Dr Zirngibl

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.)

1989-01-07

Filing date

1990-01-04

Publication date

1991-09-13

1990-01-04 Application filed by Sandoz Ag filed Critical Sandoz Ag

1991-09-13 Publication of CH678430A5 publication Critical patent/CH678430A5/de

Links

239000000975 dye Substances 0.000 claims description 43
239000000203 mixture Substances 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 17
239000001257 hydrogen Substances 0.000 claims description 16
239000000460 chlorine Substances 0.000 claims description 12
238000002360 preparation method Methods 0.000 claims description 11
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 10
150000002431 hydrogen Chemical class 0.000 claims description 10
239000000986 disperse dye Substances 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 6
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
238000000034 method Methods 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims 1
150000001412 amines Chemical class 0.000 claims 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
238000004043 dyeing Methods 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000000243 solution Substances 0.000 description 5
238000001816 cooling Methods 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
229960000583 acetic acid Drugs 0.000 description 3
-1 benzylcarbonyloxy Chemical group 0.000 description 3
230000008878 coupling Effects 0.000 description 3
238000010168 coupling process Methods 0.000 description 3
238000005859 coupling reaction Methods 0.000 description 3
239000012954 diazonium Substances 0.000 description 3
150000001989 diazonium salts Chemical class 0.000 description 3
239000000463 material Substances 0.000 description 3
238000007639 printing Methods 0.000 description 3
QPQKUYVSJWQSDY-CCEZHUSRSA-N 4-(phenylazo)aniline Chemical compound C1=CC(N)=CC=C1\N=N\C1=CC=CC=C1 QPQKUYVSJWQSDY-CCEZHUSRSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000011324 bead Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000000605 extraction Methods 0.000 description 2
239000000835 fiber Substances 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
VJMAITQRABEEKP-UHFFFAOYSA-N [6-(phenylmethoxymethyl)-1,4-dioxan-2-yl]methyl acetate Chemical compound O1C(COC(=O)C)COCC1COCC1=CC=CC=C1 VJMAITQRABEEKP-UHFFFAOYSA-N 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000000889 atomisation Methods 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000009998 heat setting Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000009980 pad dyeing Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0046—Mixtures of two or more azo dyes
- C09B67/0055—Mixtures of two or more disazo dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/12—Disazo dyes from other coupling components "C"
- C09B31/14—Heterocyclic components
- C09B31/153—Heterocyclic components containing a six-membered ring with one nitrogen atom as the only ring hetero-atom
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0041—Blends of pigments; Mixtured crystals; Solid solutions mixtures containing one azo dye

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Coloring (AREA)
Pyridine Compounds (AREA)

CH20/90A 1989-01-07 1990-01-04 CH678430A5 (it)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3900309		1989-01-07

Publications (1)

Publication Number	Publication Date
CH678430A5 true CH678430A5 (it)	1991-09-13

Family

ID=6371678

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH20/90A CH678430A5 (it)	1989-01-07	1990-01-04

Country Status (6)

Country	Link
JP (1)	JPH02228366A (it)
CH (1)	CH678430A5 (it)
DE (1)	DE3942938A1 (it)
FR (1)	FR2641541A1 (it)
GB (1)	GB2226826B (it)
IT (1)	IT1239741B (it)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN107805409A (zh) *	2017-11-21	2018-03-16	江苏亚邦染料股份有限公司	一种环保型黄色分散染料组合物

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1917278B2 (de) *	1969-04-03	1974-06-27	Basf Ag, 6700 Ludwigshafen	Monoazofarbstoffe, Verfahren zu deren Herstellung und Farbstoffzubereitungen
FR2413409A1 (fr) *	1978-01-02	1979-07-27	Huels Chemische Werke Ag	Procede pour preparer des polystyrenes resistant a la chaleur, bromes sur le noyau
DE2801951A1 (de) *	1978-01-18	1979-07-19	Basf Ag	Azofarbstoffe
DE3505899A1 (de) *	1985-02-21	1986-08-21	Cassella Ag, 6000 Frankfurt	Mischung gelber dispersionsfarbstoffe

1989
- 1989-12-23 DE DE3942938A patent/DE3942938A1/de not_active Withdrawn
1990
- 1990-01-04 CH CH20/90A patent/CH678430A5/de not_active IP Right Cessation
- 1990-01-05 GB GB9000225A patent/GB2226826B/en not_active Expired - Fee Related
- 1990-01-05 JP JP2000134A patent/JPH02228366A/ja active Pending
- 1990-01-05 FR FR9000104A patent/FR2641541A1/fr not_active Withdrawn
- 1990-01-08 IT IT47511A patent/IT1239741B/it active IP Right Grant

Also Published As

Publication number	Publication date
IT9047511A1 (it)	1990-07-08
IT9047511A0 (it)	1990-01-08
IT1239741B (it)	1993-11-15
JPH02228366A (ja)	1990-09-11
FR2641541A1 (fr)	1990-07-13
GB9000225D0 (en)	1990-03-07
GB2226826A (en)	1990-07-11
GB2226826B (en)	1993-01-06
DE3942938A1 (de)	1990-07-12

Legal Events

Date	Code	Title	Description
1996-09-13	PL	Patent ceased

Publication	Publication Date	Title
DE2915323C2 (it)	1988-12-08
EP0465420B1 (de)	1996-10-30	Azofarbstoffe
EP0357560B1 (de)	1995-07-26	Anionische Triazinylamino-Disazofarbstoffe
DE3313797C2 (it)	1991-09-19
CH690648A5 (de)	2000-11-30	Monoazo-Dispersionsfarbstoffe.
CH678430A5 (it)	1991-09-13
DE60201658T2 (de)	2005-03-24	Verwendung von pigmentfarbstoffen zum dispersionsfärben aus wässrigen medien
CH663216A5 (de)	1987-11-30	Azo-pigmentfarbstoff-gemische.
DE19524134A1 (de)	1997-01-09	Verfahren zum Reduzieren der Toxizität von Restflotten und neue kationische Farbstoffe
DE2022624B2 (de)	1973-09-13	Basischer Disazofarbstoff, Ver fahren zu dessen Herstellung und dessen Verwendung
DE3405021A1 (de)	1985-08-14	Mischungen von monoazofarbstoffen
DE1644259B2 (de)	1977-07-28	In wasser schwerloesliche azofarbstoffe, verfahren zu deren herstellung und ihre verwendung zum faerben
DE1927416C3 (de)	1978-09-28	Basische Azofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
EP0387589B1 (de)	1994-04-27	Reaktivfarbstoffe, die drei reaktive Gruppen aufweisen
DE60222639T4 (de)	2008-07-10	Verwendung von pigmentfarbstoffen zur dispersionsfärbung aus wässrigen medien
DE1233520B (de)	1967-02-02	Verfahren zur Herstellung von basischen Hydrazonfarbstoffen
EP0265828A1 (de)	1988-05-04	Wasserlösliche Disazoverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Farbstoffe
EP0726297A1 (de)	1996-08-14	Farbstoffmischungen und ihre Verwendung
DE1298661B (de)	1969-07-03	Verfahren zur Herstellung in Wasser schwer loeslicher Dispersionsfarbstoffe
DE3246949C2 (it)	1989-12-07
DE2252785A1 (de)	1973-05-10	Farbstoffe mit einer sulphonylazidogruppe
DE2103361C3 (de)	1978-07-13	In Wasser schwer lösliche Monoazoverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Dispersionsfarbstoffe
DE2035002C3 (de)	1979-01-11	Monoazo-Dispersionsf arbstoffe, Verfahren zu deren Herstellung und ihre Verwendung
DE2130040B2 (de)	1979-01-04	Wasserunlösliche Monoazoverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung
AT387229B (de)	1988-12-27	Basische bzw. kationische, sulfonsaeuregruppenhaltige monoazo- oder disazoverbindungen