JPH0322423B2 - - Google Patents

Info

Publication number: JPH0322423B2
Authority: JP; Japan
Prior art keywords: alkyl; represents hydrogen; hydrogen; sulfo; following formula
Prior art date: 1980-10-07
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 - Lifetime

Application number

JP56158269A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5794051A (en

Inventor

Kotsuho Berunaa

Bureneisen Kuruto

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.)

Sandoz AG

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.)

1980-10-07

Filing date

1981-10-06

Publication date

1991-03-26

1981-10-06 Application filed by Sandoz AG filed Critical Sandoz AG

1982-06-11 Publication of JPS5794051A publication Critical patent/JPS5794051A/ja

1991-03-26 Publication of JPH0322423B2 publication Critical patent/JPH0322423B2/ja

Status Granted legal-status Critical Current

Links

239000001257 hydrogen Substances 0.000 claims description 69
229910052739 hydrogen Inorganic materials 0.000 claims description 69
150000002431 hydrogen Chemical class 0.000 claims description 32
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 28
125000000217 alkyl group Chemical group 0.000 claims description 27
150000001875 compounds Chemical class 0.000 claims description 22
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 20
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 14
239000000460 chlorine Substances 0.000 claims description 14
229910052801 chlorine Inorganic materials 0.000 claims description 14
125000002947 alkylene group Chemical group 0.000 claims description 12
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 10
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 9
-1 carboxy, sulfo, sulfomethylene Chemical group 0.000 claims description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
150000003839 salts Chemical group 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 8
238000004043 dyeing Methods 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 6
239000011737 fluorine Substances 0.000 claims description 5
229910052731 fluorine Inorganic materials 0.000 claims description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
239000000758 substrate Substances 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims 1
125000001153 fluoro group Chemical group F* 0.000 claims 1
239000000975 dye Substances 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
239000000243 solution Substances 0.000 description 12
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
238000000034 method Methods 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 6
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 5
230000007935 neutral effect Effects 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000000047 product Substances 0.000 description 4
239000011780 sodium chloride Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
229920000742 Cotton Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000001768 cations Chemical class 0.000 description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
239000000985 reactive dye Substances 0.000 description 3
239000004627 regenerated cellulose Substances 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
229920000297 Rayon Polymers 0.000 description 2
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000005185 salting out Methods 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
238000010186 staining Methods 0.000 description 2
238000005406 washing Methods 0.000 description 2
ZNXSFVXZQBETRJ-UHFFFAOYSA-N (3-aminophenyl)urea Chemical compound NC(=O)NC1=CC=CC(N)=C1 ZNXSFVXZQBETRJ-UHFFFAOYSA-N 0.000 description 1
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
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
MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
ISTNBIUEOOWHHO-UHFFFAOYSA-N 5-amino-4-hydroxy-3-[(2-sulfophenyl)diazenyl]naphthalene-2,7-disulfonic acid Chemical compound OC1=C2C(N)=CC(S(O)(=O)=O)=CC2=CC(S(O)(=O)=O)=C1N=NC1=CC=CC=C1S(O)(=O)=O ISTNBIUEOOWHHO-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
229920003043 Cellulose fiber Polymers 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
OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000006193 diazotization reaction Methods 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000010985 leather Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
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 1
239000010446 mirabilite Substances 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000002964 rayon Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 description 1
229960005369 scarlet red Drugs 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
159000000000 sodium salts Chemical group 0.000 description 1
RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
210000004243 sweat Anatomy 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
210000002268 wool Anatomy 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
- C09B62/02—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
- C09B62/043—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 containing two or more triazine rings linked together by a non-chromophoric link

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)

JP56158269A 1980-10-07 1981-10-06 Halotriazinyl-containing compound Granted JPS5794051A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB8032278		1980-10-07

Publications (2)

Publication Number	Publication Date
JPS5794051A JPS5794051A (en)	1982-06-11
JPH0322423B2 true JPH0322423B2 (es)	1991-03-26

Family

ID=10516527

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP56158269A Granted JPS5794051A (en)	1980-10-07	1981-10-06	Halotriazinyl-containing compound

Country Status (10)

Country	Link
JP (1)	JPS5794051A (es)
BE (1)	BE904413Q (es)
BR (1)	BR8106447A (es)
CH (1)	CH646989A5 (es)
DE (1)	DE3138019A1 (es)
ES (1)	ES506012A0 (es)
FR (1)	FR2491486B1 (es)
HK (1)	HK74986A (es)
IT (1)	IT1196418B (es)
MY (1)	MY8700120A (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2556358B1 (fr) *	1983-12-10	1987-01-02	Sandoz Sa	Nouveaux composes bisazoiques, leur preparation et leur utilisation comme colorants
JPH066676B2 (ja) *	1985-07-09	1994-01-26	日本化薬株式会社	アゾ化合物及びそれを用いる染色法
CH689424A5 (de) *	1994-05-06	1999-04-15	Clariant Finance Bvi Ltd	Faserreaktive Disazofarbstoffe.
JP4538904B2 (ja) *	2000-06-09	2010-09-08	住友化学株式会社	反応染料組成物およびその繊維材料への適用
TWI411650B (zh) *	2009-07-15	2013-10-11	Everlight Chem Ind Corp	具有ｎ－烷胺基的新型反應性染料

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5374186A (en) *	1976-12-13	1978-07-01	Mitsubishi Chem Ind	Dyeing of cellulosic fiber

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1228184A (fr) *	1958-03-05	1960-08-26	Ici Ltd	Nouvelles matières colorantes azoïques
GB1283771A (en) *	1969-01-16	1972-08-02	Ici Ltd	New reactive disazo dyestuffs
JPS51147688A (en) *	1975-06-10	1976-12-18	Mitsubishi Chem Ind	Dyeing method of cellulosic fiber
FR2304651A1 (fr) *	1976-03-18	1976-10-15	Ciba Geigy Ag	Colorants reactifs vis-a-vis de la fibre, leur procede de preparation et leur utilisation

1981
- 1981-09-21 CH CH607681A patent/CH646989A5/de not_active IP Right Cessation
- 1981-09-24 DE DE19813138019 patent/DE3138019A1/de active Granted
- 1981-10-05 ES ES506012A patent/ES506012A0/es active Granted
- 1981-10-05 FR FR8118837A patent/FR2491486B1/fr not_active Expired
- 1981-10-06 JP JP56158269A patent/JPS5794051A/ja active Granted
- 1981-10-07 BR BR8106447A patent/BR8106447A/pt unknown
- 1981-10-07 IT IT24370/81A patent/IT1196418B/it active
1986
- 1986-03-13 BE BE1/011456A patent/BE904413Q/fr not_active IP Right Cessation
- 1986-10-02 HK HK749/86A patent/HK74986A/xx not_active IP Right Cessation
1987
- 1987-12-30 MY MY120/87A patent/MY8700120A/xx unknown

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5374186A (en) *	1976-12-13	1978-07-01	Mitsubishi Chem Ind	Dyeing of cellulosic fiber

Also Published As

Publication number	Publication date
MY8700120A (en)	1987-12-31
CH646989A5 (de)	1984-12-28
BR8106447A (pt)	1982-06-22
IT8124370A0 (it)	1981-10-07
ES8302061A1 (es)	1983-01-01
FR2491486A1 (fr)	1982-04-09
IT1196418B (it)	1988-11-16
HK74986A (en)	1986-10-10
ES506012A0 (es)	1983-01-01
BE904413Q (fr)	1986-06-30
DE3138019C2 (es)	1988-12-08
FR2491486B1 (fr)	1986-09-05
DE3138019A1 (de)	1982-05-13
JPS5794051A (en)	1982-06-11

Publication	Publication Date	Title
KR940006572B1 (ko)	1994-07-22	피리디니오트리아지닐그룹과 비닐설폰형그룹을 함유하는 섬유반응성 화합물의 제조방법
EP0772652B1 (en)	2001-08-29	Reactive monoazo dyestuffs
US5149790A (en)	1992-09-22	Bis chlorotriazine reactive dyes containing a benzylamine linking group
JPH05247365A (ja)	1993-09-24	フルオロピリミジン反応性染料
JP2747500B2 (ja)	1998-05-06	繊維反応性フタロシアニン染料
US5410041A (en)	1995-04-25	Bisreactive dyes having a disulfophenylene bridging member
JPH0234667A (ja)	1990-02-05	繊維反応性染料
JPH0322423B2 (es)	1991-03-26
US4518391A (en)	1985-05-21	Monoazo compounds having a sulfo group-containing diazo component radical and a 6-(2'-chloro-1',3',5'-triazin-6'-ylamino)-1-hydroxy-3-sulfonaphthalene coupling component radical having a substituted amino group in the 4'-position
JPS6025064B2 (ja)	1985-06-15	ジスアゾ染料
US4284554A (en)	1981-08-18	Monoazo compounds having a 6-(2'-N-alkylanilino--4-chloro-1',3',5'-triazinyl-6'-amino or alkylamino)-1-hydroxy-3-sulfonaphthalene coupling component radical
US5847111A (en)	1998-12-08	Aluminum phthalocyanine reactive dyes
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
US4129736A (en)	1978-12-12	Triazinyl-antraquinone dyestuffs
CA2244106C (en)	2005-09-20	Fibre-reactive dyestuffs
US20040087780A1 (en)	2004-05-06	Monoazo reactive red dyestuff
JPH09176505A (ja)	1997-07-08	反応性染料及びそれらを製造する方法
US5223607A (en)	1993-06-29	Reactive azo dyes with at lest two reactive halotriazine groups
US5227478A (en)	1993-07-13	2-chloro-4-[4'-(4",8"-disulfonaphth-2"-ylazo)-2'-methoxy-5'-methylanilino]-6
JPH07150060A (ja)	1995-06-13	多官能性アゾ型反応性染料
US4033944A (en)	1977-07-05	Fibre-reactive hydroxycycloalkenyl-halo triazinyl containing dyestuffs
KR100294994B1 (ko)	2001-11-30	섬유-반응성모노아조염료
KR890003581B1 (ko)	1989-09-25	동모노아조 착화합물의 제조방법
JPH0798908B2 (ja)	1995-10-25	水溶性アゾ化合物、その製法及び該化合物を染料として使用する方法
KR900004222B1 (ko)	1990-06-18	반응성 디스아조 염료의 제조방법