SU416954A3 - Способ получения дисазокрасителя - Google Patents

Способ получения дисазокрасителя

Info

Publication number: SU416954A3
Authority: SU; USSR - Soviet Union
Prior art keywords: dye; acid; group; residue; solution
Prior art date: 1968-11-04

Application number

SU1375072A

Other languages

English (en)

Russian (ru)

Original Assignee

Иностранцы Фритц Эстерлейн , Карл Сейц

Иностранна фирма Циба Гейги

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.)

1968-11-04

Filing date

1969-11-03

Publication date

1974-02-25

1969-11-03 Application filed by Иностранцы Фритц Эстерлейн , Карл Сейц, Иностранна фирма Циба Гейги filed Critical Иностранцы Фритц Эстерлейн , Карл Сейц

1974-02-25 Application granted granted Critical

1974-02-25 Publication of SU416954A3 publication Critical patent/SU416954A3/ru

Links

238000000034 method Methods 0.000 title description 8
239000000975 dye Substances 0.000 description 14
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
239000000243 solution Substances 0.000 description 10
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 6
239000000835 fiber Substances 0.000 description 5
239000002253 acid Substances 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
QPILZZVXGUNELN-UHFFFAOYSA-M sodium;4-amino-5-hydroxynaphthalene-2,7-disulfonate;hydron Chemical compound [Na+].OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S([O-])(=O)=O)=CC2=C1 QPILZZVXGUNELN-UHFFFAOYSA-M 0.000 description 3
ZMCHBSMFKQYNKA-UHFFFAOYSA-N 2-aminobenzenesulfonic acid Chemical compound NC1=CC=CC=C1S(O)(=O)=O ZMCHBSMFKQYNKA-UHFFFAOYSA-N 0.000 description 2
FOINSAWEWXUXPQ-UHFFFAOYSA-N 4-acetamido-2-aminobenzenesulfonic acid Chemical compound CC(=O)NC1=CC=C(S(O)(=O)=O)C(N)=C1 FOINSAWEWXUXPQ-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
239000003929 acidic solution Substances 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
238000006193 diazotization reaction Methods 0.000 description 2
239000004744 fabric Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
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 description 2
239000000203 mixture Substances 0.000 description 2
239000003973 paint Substances 0.000 description 2
235000010288 sodium nitrite Nutrition 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
125000000542 sulfonic acid group Chemical group 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
-1 1-amino-8-hydroxynaphthalene-3,6-disulfonic acid diazo compound Chemical class 0.000 description 1
JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 description 1
ONKKHWSNAANHPQ-UHFFFAOYSA-N 4,6-dichloro-5-(2-methoxyethoxy)triazine Chemical compound COCCOC1=C(Cl)N=NN=C1Cl ONKKHWSNAANHPQ-UHFFFAOYSA-N 0.000 description 1
APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 description 1
CQIJFPCXYYGGDY-UHFFFAOYSA-N 4-chloro-5-methoxytriazine Chemical group COC=1C(=NN=NC1)Cl CQIJFPCXYYGGDY-UHFFFAOYSA-N 0.000 description 1
241000282887 Suidae Species 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000008049 diazo compounds Chemical class 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
SQYUJKVKVFILNB-UHFFFAOYSA-N methyl 2-amino-4-[(2,5-dichlorophenyl)carbamoyl]benzoate Chemical compound C1=C(N)C(C(=O)OC)=CC=C1C(=O)NC1=CC(Cl)=CC=C1Cl SQYUJKVKVFILNB-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000004753 textile Substances 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/4401—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
- C09B62/4411—Azo dyes
- C09B62/4415—Disazo or polyazo 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
- C09B62/006—Azodyes
- C09B62/01—Disazo or polyazo 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/08—Azo dyes
- C09B62/09—Disazo or polyazo dyes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

SU1375072A 1968-11-04 1969-11-03 Способ получения дисазокрасителя SU416954A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1638368A CH527258A (de)	1968-11-04	1968-11-04	Verfahren zur Herstellung von Disazoverbindungen

Publications (1)

Publication Number	Publication Date
SU416954A3 true SU416954A3 (ru)	1974-02-25

Family

ID=4416885

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1375072A SU416954A3 (ru)	1968-11-04	1969-11-03	Способ получения дисазокрасителя

Country Status (10)

Country	Link
BE (1)	BE741185A (de)
BR (1)	BR6913841D0 (de)
CH (1)	CH527258A (de)
CS (1)	CS189564B2 (de)
DE (1)	DE1954269A1 (de)
FR (1)	FR2022498A1 (de)
GB (1)	GB1292620A (de)
NL (1)	NL6916534A (de)
PL (1)	PL80407B1 (de)
SU (1)	SU416954A3 (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5331732A (en) *	1976-09-06	1978-03-25	Nippon Kayaku Co Ltd	Preparation of bisazo dye
CH638555A5 (de) *	1978-06-19	1983-09-30	Ciba Geigy Ag	Reaktivfarbstoffe und deren herstellung.

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1181425A (fr) *	1956-06-29	1959-06-16	Ciba Geigy	Nouveaux colorants azoïques, leur préparation et leurs emplois

1968
- 1968-11-04 CH CH1638368A patent/CH527258A/de not_active IP Right Cessation
1969
- 1969-10-15 FR FR6935237A patent/FR2022498A1/fr not_active Withdrawn
- 1969-10-22 CS CS699869A patent/CS189564B2/cs unknown
- 1969-10-23 GB GB5199669A patent/GB1292620A/en not_active Expired
- 1969-10-28 DE DE19691954269 patent/DE1954269A1/de active Pending
- 1969-11-03 SU SU1375072A patent/SU416954A3/ru active
- 1969-11-03 BE BE741185D patent/BE741185A/xx not_active IP Right Cessation
- 1969-11-03 BR BR21384169A patent/BR6913841D0/pt unknown
- 1969-11-03 PL PL13665769A patent/PL80407B1/pl unknown
- 1969-11-03 NL NL6916534A patent/NL6916534A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE1954269A1 (de)	1970-06-04
PL80407B1 (de)	1975-08-30
CS189564B2 (en)	1979-04-30
NL6916534A (de)	1970-05-08
BE741185A (de)	1970-05-04
BR6913841D0 (pt)	1973-04-12
CH527258A (de)	1972-08-31
GB1292620A (en)	1972-10-11
FR2022498A1 (de)	1970-07-31

Publication	Publication Date	Title
NO124964B (de)	1972-06-26
DE2557141A1 (de)	1976-07-01	Reaktivfarbstoffe, deren herstellung und verwendung
DE2500062C2 (de)	1986-02-20	Faserreaktive Tetrazofarbstoffe und ihre Verwendung
KR100614820B1 (ko)	2006-08-25	연결을 함유하는 반응성 염료
US4038267A (en)	1977-07-26	Triazine reactive dyes
KR840000609B1 (ko)	1984-04-28	반응성 염료의 제조 방법
SU416954A3 (ru)	1974-02-25	Способ получения дисазокрасителя
GB2148921A (en)	1985-06-05	New formazan reactive dyes
US3163635A (en)	1964-12-29	Water-soluble azo dyestuffs
JPS58142940A (ja)	1983-08-25	反応染料と，その製造法および用法
DE2601043A1 (de)	1976-07-22	Tetrareaktive disazofarbstoffe, deren herstellung und verwendung
US4338092A (en)	1982-07-06	Disazo compounds having a 4,6,8-trisulfonaphthyl diazo components radical and a 2-amino or substituted amino-4-chloro-1,3,5-triazin-6-yl-amino substituent
JPS5929621B2 (ja)	1984-07-21	繊維反応性ジスアゾ染料およびその製法
US3709869A (en)	1973-01-09	Reactive triazine azo dyestuffs
US2842536A (en)	1958-07-08	Metallized disazo dyes
US5095101A (en)	1992-03-10	1-Amino-2,7-di-[5'-(2"-chloro-4"-substituted amino-1,3,5-triazin-6"-ylamino)-2'-sulfophenylazo]-3,6-disulfonic acids
EP0170612B1 (de)	1989-05-24	Reaktivfarbstoffe, deren Herstellung und Verwendung
US4148790A (en)	1979-04-10	Metallized triazine reactive dyes
US3310551A (en)	1967-03-21	Azostilbene dyestuffs
US2741655A (en)	1956-04-10	Cupriferous azo-dyestuffs
US5227478A (en)	1993-07-13	2-chloro-4-[4'-(4",8"-disulfonaphth-2"-ylazo)-2'-methoxy-5'-methylanilino]-6
US2714588A (en)	1955-08-02	Copper-containing disazo dyestuffs
GB2028360A (en)	1980-03-05	Fibre-reactive azo dyes, processes for their manufacture and use thereof
KR100294994B1 (ko)	2001-11-30	섬유-반응성모노아조염료
KR100352808B1 (ko)	2002-12-18	섬유반응성디스아조염료