CA1274506A - Methode de preparation de solutions de colorants rouges anioniques en concentration - Google Patents

Methode de preparation de solutions de colorants rouges anioniques en concentration

Info

Publication number: CA1274506A
Authority: CA; Canada
Prior art keywords: dye; so2n; water soluble; lower alkyl; weight
Prior art date: 1986-01-30
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 - Fee Related

Application number

CA000527134A

Other languages

English (en)

Inventor

Jay E. Rowe

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.)

Crompton and Knowles Corp

Original Assignee

Crompton and Knowles Corp

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.)

1986-01-30

Filing date

1987-01-12

Publication date

1990-09-25

1986-01-30 Priority claimed from US06/824,306 external-priority patent/US4654045A/en

1987-01-12 Application filed by Crompton and Knowles Corp filed Critical Crompton and Knowles Corp

1990-09-25 Application granted granted Critical

1990-09-25 Publication of CA1274506A publication Critical patent/CA1274506A/fr

2007-09-25 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 39
125000000129 anionic group Chemical group 0.000 title claims abstract description 13
238000002360 preparation method Methods 0.000 title claims abstract description 4
239000001044 red dye Substances 0.000 title abstract description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
239000000203 mixture Substances 0.000 claims abstract description 16
125000000217 alkyl group Chemical group 0.000 claims abstract description 10
239000003960 organic solvent Substances 0.000 claims abstract description 9
150000001412 amines Chemical class 0.000 claims abstract description 8
QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical group COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 claims description 6
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 5
WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical group COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
239000003021 water soluble solvent Substances 0.000 claims 1
239000000975 dye Substances 0.000 abstract description 52
238000003860 storage Methods 0.000 abstract description 9
238000004519 manufacturing process Methods 0.000 abstract description 7
150000003839 salts Chemical class 0.000 description 10
239000007788 liquid Substances 0.000 description 9
239000002253 acid Substances 0.000 description 8
238000004043 dyeing Methods 0.000 description 7
239000004677 Nylon Substances 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
239000013078 crystal Substances 0.000 description 6
229920001778 nylon Polymers 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
239000011734 sodium Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
239000008367 deionised water Substances 0.000 description 4
229910021641 deionized water Inorganic materials 0.000 description 4
-1 for example Substances 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
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 3
150000001346 alkyl aryl ethers Chemical class 0.000 description 3
150000001768 cations Chemical class 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 3
239000000835 fiber Substances 0.000 description 3
239000012065 filter cake Substances 0.000 description 3
238000001914 filtration Methods 0.000 description 3
JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
239000002585 base Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
229960004063 propylene glycol Drugs 0.000 description 2
235000013772 propylene glycol Nutrition 0.000 description 2
238000000926 separation method Methods 0.000 description 2
230000003245 working effect Effects 0.000 description 2
241001465754 Metazoa Species 0.000 description 1
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
238000010669 acid-base reaction Methods 0.000 description 1
230000002411 adverse Effects 0.000 description 1
230000032683 aging Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
238000010960 commercial process Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002829 nitrogen Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000003791 organic solvent mixture Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
GVLHHJPRNMDLLL-UHFFFAOYSA-M sodium 7-amino-8-[[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-3-sulfonaphthalen-1-olate Chemical compound NC1=CC=C2C=C(C=C(O)C2=C1N=NC1=CC=C(Cl)C=C1C(F)(F)F)S(=O)(=O)O[Na] GVLHHJPRNMDLLL-UHFFFAOYSA-M 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000004753 textile Substances 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000759 toxicological effect Toxicity 0.000 description 1
238000004148 unit process Methods 0.000 description 1

Landscapes

Coloring (AREA)

CA000527134A 1986-01-30 1987-01-12 Methode de preparation de solutions de colorants rouges anioniques en concentration Expired - Fee Related CA1274506A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/824,306 US4654045A (en)	1985-05-03	1986-01-30	Process for preparation of concentrated anionic red dye solutions
US824,306		1986-01-30

Publications (1)

Publication Number	Publication Date
CA1274506A true CA1274506A (fr)	1990-09-25

Family

ID=25241068

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000527134A Expired - Fee Related CA1274506A (fr)	1986-01-30	1987-01-12	Methode de preparation de solutions de colorants rouges anioniques en concentration

Country Status (2)

Country	Link
JP (1)	JPS63189470A (fr)
CA (1)	CA1274506A (fr)

1987
- 1987-01-12 CA CA000527134A patent/CA1274506A/fr not_active Expired - Fee Related
- 1987-01-22 JP JP1149387A patent/JPS63189470A/ja active Pending

Also Published As

Publication number	Publication date
JPS63189470A (ja)	1988-08-05

Legal Events

Date	Code	Title	Description
1998-09-25	MKLA	Lapsed

Publication	Publication Date	Title
CH352655A (de)	1961-03-15	Verfahren zur Erhöhung der Beständigkeit von dihalogentriazingruppenhaltigen Verbindungen
DE2460491A1 (de)	1976-07-01	Verfahren zur herstellung von xanthenfarbstoffen
EP0075905A2 (fr)	1983-04-06	Composés réactifs, solubles dans l'eau, de la série des phtalocyanines, procédé pour leur préparation et leur utilisation comme colorants
EP0039439B1 (fr)	1983-12-07	Procédé de fabrication de colorants solubles dans l'eau, à faible teneur en sels
CA1274506A (fr)	1990-09-25	Methode de preparation de solutions de colorants rouges anioniques en concentration
US4654045A (en)	1987-03-31	Process for preparation of concentrated anionic red dye solutions
EP0922038B1 (fr)	2002-02-06	Procede de preparation de sels substitues de 4,4'-diaminostilbene-2,2'-acide disulfonique
EP0276534A1 (fr)	1988-08-03	Procédé de préparation de solutions concentrées d'un colorant anionique rouge
DE1569727A1 (de)	1970-05-14	Verfahren zur Herstellung von Farbstoffen
EP0703281A1 (fr)	1996-03-27	Procédé de fabrication de phtalocyanine de métal bromées et substituées par des alcoxy
US4120789A (en)	1978-10-17	Method for the purification of sewage waters which contain organic compounds of an anionic nature
DE1070313B (de)	1959-12-03	Verfahren zur Herstellung von 1-Amino-4- phenylamino- anthrachinon- 2- sulfonsäuren
EP0603129B1 (fr)	1999-09-29	Colorants oxaziniques, procédé de leur préparation et leur utilisation
DE44002C (de)		Verfahren zur Darstellung von Farbstoffen aus der Gruppe des Metaam dophenol-Phtaleins
CH624978A5 (en)	1981-08-31	Process for the preparation of chromium or cobalt complex dyes
EP0950692A1 (fr)	1999-10-20	Composés azoiques, procédé pour leur préparation et leur utilisation comme colorants réactifs sur la fibre
AT321926B (de)	1975-04-25	Verfahren zur herstellung von pyridazinon-derivaten mit herbizider wirkung
EP0957138B1 (fr)	2001-12-05	Solutions de colorants du type anthraquinone bleu, stables au stockage et pouvoir colorant élevé
GB1569837A (en)	1980-06-18	Phthalocyanine pigments
DE1259286B (de)	1968-01-25	Verfahren zum Faerben und Bedrucken von natuerlichen und synthetischen Polyamidfasern
DE2242784B2 (de)	1978-01-19	Verfahren zur herstellung von 2-aryl-v-triazolen
DE1569727C (de)	1972-11-16	Verfahren zur Herstellung von Phthalocyaninfarbstoffen
DE891309C (de)	1953-09-28	Verfahren zur Herstellung von Sulfonsaeuren der Phthalocyaninreihe
KR100791955B1 (ko)	2008-01-04	안정한 1,2-벤즈이소티아졸린-3-온 액상 조성물과 이의제조방법
DE85232C (fr)