ES256010A1 - Procedimiento para la preparaciën de derivados de colorantes polihidroxilados estables - Google Patents

Procedimiento para la preparaciën de derivados de colorantes polihidroxilados estables

Info

Publication number: ES256010A1
Authority: ES; Spain
Prior art keywords: reactive; dyestuff; soluble; reaction; coupling
Prior art date: 1959-02-12
Legal status (The legal status 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 status listed.): Expired

Application number

ES0256010A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

BASF Schweiz AG

Original Assignee

Ciba Geigy AG

Ciba 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.)

1959-02-12

Filing date

1960-02-11

Publication date

1960-08-16

1960-01-12 Priority claimed from CH25460A external-priority patent/CH398835A/de

1960-02-11 Application filed by Ciba Geigy AG, Ciba AG filed Critical Ciba Geigy AG

1960-08-16 Publication of ES256010A1 publication Critical patent/ES256010A1/es

Status Expired legal-status Critical Current

Links

239000000975 dye Substances 0.000 title abstract 13
239000007795 chemical reaction product Substances 0.000 title abstract 10
230000008878 coupling Effects 0.000 abstract 7
238000010168 coupling process Methods 0.000 abstract 7
238000005859 coupling reaction Methods 0.000 abstract 7
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
-1 methyl- Chemical group 0.000 abstract 5
229920002472 Starch Polymers 0.000 abstract 4
238000006243 chemical reaction Methods 0.000 abstract 4
238000006193 diazotization reaction Methods 0.000 abstract 4
238000004043 dyeing Methods 0.000 abstract 4
235000019698 starch Nutrition 0.000 abstract 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
239000002253 acid Substances 0.000 abstract 3
239000003513 alkali Substances 0.000 abstract 3
150000001412 amines Chemical class 0.000 abstract 3
239000011230 binding agent Substances 0.000 abstract 3
239000008107 starch Substances 0.000 abstract 3
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 abstract 2
239000004375 Dextrin Substances 0.000 abstract 2
229920001353 Dextrin Polymers 0.000 abstract 2
229920002907 Guar gum Polymers 0.000 abstract 2
229920000084 Gum arabic Polymers 0.000 abstract 2
239000004354 Hydroxyethyl cellulose Substances 0.000 abstract 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 abstract 2
239000004372 Polyvinyl alcohol Substances 0.000 abstract 2
229920000297 Rayon Polymers 0.000 abstract 2
241000978776 Senegalia senegal Species 0.000 abstract 2
235000010489 acacia gum Nutrition 0.000 abstract 2
239000000205 acacia gum Substances 0.000 abstract 2
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 2
150000004056 anthraquinones Chemical class 0.000 abstract 2
125000004429 atom Chemical group 0.000 abstract 2
229920002678 cellulose Polymers 0.000 abstract 2
239000001913 cellulose Substances 0.000 abstract 2
229920003086 cellulose ether Polymers 0.000 abstract 2
235000019425 dextrin Nutrition 0.000 abstract 2
235000010417 guar gum Nutrition 0.000 abstract 2
125000005843 halogen group Chemical group 0.000 abstract 2
229920006158 high molecular weight polymer Polymers 0.000 abstract 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 abstract 2
235000010987 pectin Nutrition 0.000 abstract 2
239000001814 pectin Substances 0.000 abstract 2
229920001277 pectin Polymers 0.000 abstract 2
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract 2
229920000642 polymer Polymers 0.000 abstract 2
229920002451 polyvinyl alcohol Polymers 0.000 abstract 2
239000001117 sulphuric acid Substances 0.000 abstract 2
235000011149 sulphuric acid Nutrition 0.000 abstract 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 abstract 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 abstract 1
FJNZOTVFXOADDQ-UHFFFAOYSA-N 1-nitro-10h-acridin-9-one Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=CC=C2[N+](=O)[O-] FJNZOTVFXOADDQ-UHFFFAOYSA-N 0.000 abstract 1
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 abstract 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 abstract 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract 1
229920002284 Cellulose triacetate Polymers 0.000 abstract 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
229920000742 Cotton Polymers 0.000 abstract 1
239000004593 Epoxy Substances 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
229920000715 Mucilage Polymers 0.000 abstract 1
UFZWQBCMKWPPLY-UHFFFAOYSA-N N-[2-[2-(prop-2-enoylamino)ethenylsulfonyl]ethenyl]prop-2-enamide Chemical compound C(C=C)(=O)NC=CS(=O)(=O)C=CNC(C=C)=O UFZWQBCMKWPPLY-UHFFFAOYSA-N 0.000 abstract 1
229910019142 PO4 Inorganic materials 0.000 abstract 1
239000004952 Polyamide Substances 0.000 abstract 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
239000000853 adhesive Substances 0.000 abstract 1
230000001476 alcoholic effect Effects 0.000 abstract 1
235000010443 alginic acid Nutrition 0.000 abstract 1
229920000615 alginic acid Polymers 0.000 abstract 1
150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
239000012736 aqueous medium Substances 0.000 abstract 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 abstract 1
230000015572 biosynthetic process Effects 0.000 abstract 1
150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
229920002301 cellulose acetate Polymers 0.000 abstract 1
150000008049 diazo compounds Chemical class 0.000 abstract 1
IQSNOIVVWRWZEQ-UHFFFAOYSA-N ethene (isocyanatohydrazinylidene)-oxomethane Chemical compound N(N=C=O)N=C=O.C=C IQSNOIVVWRWZEQ-UHFFFAOYSA-N 0.000 abstract 1
239000011521 glass Substances 0.000 abstract 1
150000004676 glycans Chemical class 0.000 abstract 1
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 abstract 1
125000000623 heterocyclic group Chemical group 0.000 abstract 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 abstract 1
238000004519 manufacturing process Methods 0.000 abstract 1
238000000034 method Methods 0.000 abstract 1
238000006386 neutralization reaction Methods 0.000 abstract 1
239000002245 particle Substances 0.000 abstract 1
DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 abstract 1
235000021317 phosphate Nutrition 0.000 abstract 1
150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
229920002239 polyacrylonitrile Polymers 0.000 abstract 1
229920002647 polyamide Polymers 0.000 abstract 1
229920000728 polyester Polymers 0.000 abstract 1
229920001282 polysaccharide Polymers 0.000 abstract 1
239000005017 polysaccharide Substances 0.000 abstract 1
239000000047 product Substances 0.000 abstract 1
HCJTYESURSHXNB-UHFFFAOYSA-N propynamide Chemical compound NC(=O)C#C HCJTYESURSHXNB-UHFFFAOYSA-N 0.000 abstract 1
125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
239000002964 rayon Substances 0.000 abstract 1
235000010413 sodium alginate Nutrition 0.000 abstract 1
239000000661 sodium alginate Substances 0.000 abstract 1
229940005550 sodium alginate Drugs 0.000 abstract 1
VILMUCRZVVVJCA-UHFFFAOYSA-M sodium glycolate Chemical compound [Na+].OCC([O-])=O VILMUCRZVVVJCA-UHFFFAOYSA-M 0.000 abstract 1
235000011121 sodium hydroxide Nutrition 0.000 abstract 1
159000000000 sodium salts Chemical class 0.000 abstract 1
239000000725 suspension Substances 0.000 abstract 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 abstract 1
235000013311 vegetables Nutrition 0.000 abstract 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
- D06P1/0056—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
- D06P1/0064—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using reactive polyfunctional compounds, e.g. crosslinkers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/20—Post-etherification treatments of chemical or physical type, e.g. mixed etherification in two steps, including purification
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/06—Dyes

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Materials Engineering (AREA)
Biochemistry (AREA)
General Chemical & Material Sciences (AREA)
Textile Engineering (AREA)
Molecular Biology (AREA)
General Health & Medical Sciences (AREA)
Manufacturing & Machinery (AREA)
Structural Engineering (AREA)
Coloring (AREA)
Paper (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)

ES0256010A 1959-02-12 1960-02-11 Procedimiento para la preparaciën de derivados de colorantes polihidroxilados estables Expired ES256010A1 (es)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH6947459		1959-02-12
CH7459259		1959-06-18
CH25460A CH398835A (de)	1960-01-12	1960-01-12	Verfahren zur Herstellung von polyhydroxylierten Farbstoffen

Publications (1)

Publication Number	Publication Date
ES256010A1 true ES256010A1 (es)	1960-08-16

Family

ID=27171947

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0256010A Expired ES256010A1 (es)	1959-02-12	1960-02-11	Procedimiento para la preparaciën de derivados de colorantes polihidroxilados estables

Country Status (4)

Country	Link
BE (1)	BE587495A (fr)
DE (1)	DE1298658B (fr)
ES (1)	ES256010A1 (fr)
GB (1)	GB900752A (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1167083A (en) *	1966-01-20	1969-10-15	Warner Lambert Pharmaceutical	Assay Method for Amylase
US4374641A (en)	1979-08-01	1983-02-22	Badische Corporation	Polymeric color concentrates for thermoplastic polymeric materials
GB8401166D0 (en) *	1984-01-17	1984-02-22	Bevaloid Ltd	Labelled polymer compositions
EP1310533B2 (fr) *	2001-10-25	2011-07-27	Agfa Graphics N.V.	Composition d'encre contenant un type spécial de colorant et procédé d'impression par jet correspondant
CN115960021B (zh) *	2023-02-09	2023-10-20	胜利油田物华化工厂	一种用于提高原油采收率的稠油降粘剂及其合成方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2733236A (en) *		1956-01-31		Azo dyestuffs derived from dextran
BE566099A (fr) *

1960
- 1960-02-11 DE DE1960C0020778 patent/DE1298658B/de active Pending
- 1960-02-11 BE BE587495A patent/BE587495A/fr unknown
- 1960-02-11 ES ES0256010A patent/ES256010A1/es not_active Expired
- 1960-02-12 GB GB510860A patent/GB900752A/en not_active Expired

Also Published As

Publication number	Publication date
BE587495A (fr)	1960-08-11
DE1298658B (de)	1969-07-03
GB900752A (en)	1962-07-11

Publication	Publication Date	Title
NO159386B (no)	1988-09-12	Etere og estere av polygalaktomannan fra cassia tora, samt fremgangsmaate til deres fremstilling og anvendelse av forbindelsene.
US3758470A (en)	1973-09-11	Triazinyl anthraquinones
ES256010A1 (es)	1960-08-16	Procedimiento para la preparaciën de derivados de colorantes polihidroxilados estables
US2744894A (en)	1956-05-08	Hydroxyalkylation of polysaccharides
MXPA95002536A (es)	2002-10-30	Composicion de goma guar y proceso para elaborarla.
FI94764B (fi)	1995-07-14	Karboksimetyylisulfoetyyliselluloosa ja menetelmä sen valmistamiseksi
WO2000008104A1 (fr)	2000-02-17	Colorants reactifs contenant une liaison
Andrews et al.	1949	523. Experiments on the synthesis of purine nucleosides. Part XXVI. 9-D-Glucopyranosidoisoguanine
US2907762A (en)	1959-10-06	New anthraquinonoid dyestuffs
FI67860B (fi)	1985-02-28	Fosfonmetylsubstituent innehaollande vattenloesliga cellulosablandetrar och foerfarande foer framstaellning av dem
GB292452A (en)	1928-06-14	Improvements in or relating to the dyeing, printing and stencilling of materials made of or containing cellulose derivatives
GB1009911A (en)	1965-11-17	Highly polymeric dyestuffs and process for their manufacture
US2964520A (en)	1960-12-13	Water-insoluble dyestuffs of the monohalogeno-triazine-amino alkylene amino-azobenzene series
Partain	2000	Industrially important polysaccharides
US2794797A (en)	1957-06-04	Metallisable azo dyestuffs
CN1200033C (zh)	2005-05-04	水溶性羟丙基羧甲基魔芋增稠剂的制备方法
US3898033A (en)	1975-08-05	Novel disazo dyes and aqueous concentrated solutions thereof
US1896892A (en)	1933-02-07	Cellulose derivatives and process of making same
US2523709A (en)	1950-09-26	High-viscosity starch ethers and process of preparing same
US3256268A (en)	1966-06-14	Copper-containing naphthol-azonaphthol reactive dyestuffs
GB825912A (en)	1959-12-23	New colouration process for artificial fibres
US3133911A (en)	1964-05-19	Reactive dyestuffs
GB825017A (en)	1959-12-09	Textile colouration process
CS274026B1 (en)	1991-04-11	Two-sodium salt of 0-(4-chloro-6-/benzenase-2-(1-hydroxy-3,6-bisulfonate-8-yl)amino/-1,3,5-triazine-2-yl)d-galacturonane with relative polymerization degree 10 and method of its preparation
US3093628A (en)	1963-06-11	Monoazo diphenyl triazine dyestuffs