JPS5851553B2 - セルロ−スケイセンイノセンシヨクホウ - Google Patents

セルロ−スケイセンイノセンシヨクホウ

Info

Publication number: JPS5851553B2
Authority: JP; Japan
Prior art keywords: group; parts; acid; dye; formula
Prior art date: 1975-09-29
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

JP50116415A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5240687A (en

Inventor

照仁外越

正紘平木

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.)

Nippon Kayaku Co Ltd

Original Assignee

Nippon Kayaku Co Ltd

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.)

1975-09-29

Filing date

1975-09-29

Publication date

1983-11-17

1975-09-29 Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd

1975-09-29 Priority to JP50116415A priority Critical patent/JPS5851553B2/ja

1976-09-17 Priority to GB3868376A priority patent/GB1543356A/en

1976-09-27 Priority to FR7629006A priority patent/FR2325698A1/fr

1976-09-28 Priority to DE19762643673 priority patent/DE2643673A1/de

1976-09-28 Priority to BE170995A priority patent/BE846653A/fr

1976-09-28 Priority to CH1225376A priority patent/CH624136A5/de

1977-03-29 Publication of JPS5240687A publication Critical patent/JPS5240687A/ja

1983-11-17 Publication of JPS5851553B2 publication Critical patent/JPS5851553B2/ja

Status Expired legal-status Critical Current

Links

229920002678 cellulose Polymers 0.000 title 1
239000001913 cellulose Substances 0.000 title 1
239000002253 acid Substances 0.000 claims description 33
238000004043 dyeing Methods 0.000 claims description 21
239000011230 binding agent Substances 0.000 claims description 14
238000000034 method Methods 0.000 claims description 11
229920003043 Cellulose fiber Polymers 0.000 claims description 6
239000000985 reactive dye Substances 0.000 claims description 4
125000000542 sulfonic acid group Chemical group 0.000 claims description 4
150000007824 aliphatic compounds Chemical group 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
150000001491 aromatic compounds Chemical group 0.000 claims description 3
125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical group C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
229910052802 copper Inorganic materials 0.000 claims description 2
239000010949 copper Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims 1
239000000975 dye Substances 0.000 description 29
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
238000005406 washing Methods 0.000 description 10
238000002845 discoloration Methods 0.000 description 8
239000000835 fiber Substances 0.000 description 8
-1 disazo compound Chemical class 0.000 description 7
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
229920000742 Cotton Polymers 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
238000004040 coloring Methods 0.000 description 5
238000001035 drying Methods 0.000 description 5
230000007935 neutral effect Effects 0.000 description 5
239000000243 solution Substances 0.000 description 5
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
239000004202 carbamide Substances 0.000 description 4
230000008878 coupling Effects 0.000 description 4
238000010168 coupling process Methods 0.000 description 4
238000005859 coupling reaction Methods 0.000 description 4
229910017053 inorganic salt Inorganic materials 0.000 description 4
RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical class C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
239000002657 fibrous material Substances 0.000 description 3
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 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
VEXDRERIMPLZLU-UHFFFAOYSA-N 3-hydroxy-2-methylbutanoic acid Chemical compound CC(O)C(C)C(O)=O VEXDRERIMPLZLU-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000002585 base Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 2
239000004744 fabric Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000661 sodium alginate Substances 0.000 description 2
235000010413 sodium alginate Nutrition 0.000 description 2
229940005550 sodium alginate Drugs 0.000 description 2
210000004243 sweat Anatomy 0.000 description 2
239000000271 synthetic detergent Substances 0.000 description 2
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
150000004992 toluidines Chemical class 0.000 description 2
GWIAAIUASRVOIA-UHFFFAOYSA-N 2-aminonaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(N)=CC=C21 GWIAAIUASRVOIA-UHFFFAOYSA-N 0.000 description 1
YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical group N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-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
WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
FEPBITJSIHRMRT-UHFFFAOYSA-N 4-hydroxybenzenesulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C=C1 FEPBITJSIHRMRT-UHFFFAOYSA-N 0.000 description 1
CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
230000000397 acetylating effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001334 alicyclic compounds Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
BEHLMOQXOSLGHN-UHFFFAOYSA-N benzenamine sulfate Chemical compound OS(=O)(=O)NC1=CC=CC=C1 BEHLMOQXOSLGHN-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
OXMVLGLNXOXNTF-UHFFFAOYSA-N chloro(phenyl)sulfamic acid Chemical compound OS(=O)(=O)N(Cl)C1=CC=CC=C1 OXMVLGLNXOXNTF-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
ZURAKLKIKYCUJU-UHFFFAOYSA-N copper;azane Chemical compound N.[Cu+2] ZURAKLKIKYCUJU-UHFFFAOYSA-N 0.000 description 1
239000003599 detergent Substances 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000011487 hemp Substances 0.000 description 1
150000002391 heterocyclic compounds Chemical group 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000009940 knitting Methods 0.000 description 1
239000000203 mixture Substances 0.000 description 1
BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000002791 soaking Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
235000019983 sodium metaphosphate Nutrition 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000010025 steaming Methods 0.000 description 1
229960003080 taurine Drugs 0.000 description 1
239000004753 textile Substances 0.000 description 1
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
229910000406 trisodium phosphate Inorganic materials 0.000 description 1
235000019801 trisodium phosphate Nutrition 0.000 description 1
238000009941 weaving Methods 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
- C09B62/08—Azo dyes
- C09B62/095—Metal complex azo dyes

Landscapes

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

JP50116415A 1975-09-29 1975-09-29 セルロ−スケイセンイノセンシヨクホウ Expired JPS5851553B2 (ja)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
JP50116415A JPS5851553B2 (ja)	1975-09-29	1975-09-29	セルロ−スケイセンイノセンシヨクホウ
GB3868376A GB1543356A (en)	1975-09-29	1976-09-17	Copper complex reactive disazo dyestuffs
FR7629006A FR2325698A1 (fr)	1975-09-29	1976-09-27	Nouveaux colorants disazoiques reactifs et leur utilisation pour la teinture de fibres cellulosiques
DE19762643673 DE2643673A1 (de)	1975-09-29	1976-09-28	Reaktive kupferhaltige disazofarbstoffe
BE170995A BE846653A (fr)	1975-09-29	1976-09-28	Nouveaux colorants reactifs
CH1225376A CH624136A5 (en)	1975-09-29	1976-09-28	Process for the preparation of novel reactive dyes of the disazo series

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP50116415A JPS5851553B2 (ja)	1975-09-29	1975-09-29	セルロ−スケイセンイノセンシヨクホウ

Publications (2)

Publication Number	Publication Date
JPS5240687A JPS5240687A (en)	1977-03-29
JPS5851553B2 true JPS5851553B2 (ja)	1983-11-17

Family

ID=14686492

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP50116415A Expired JPS5851553B2 (ja)	1975-09-29	1975-09-29	セルロ−スケイセンイノセンシヨクホウ

Country Status (6)

Country	Link
JP (1)	JPS5851553B2 (fr)
BE (1)	BE846653A (fr)
CH (1)	CH624136A5 (fr)
DE (1)	DE2643673A1 (fr)
FR (1)	FR2325698A1 (fr)
GB (1)	GB1543356A (fr)

1975
- 1975-09-29 JP JP50116415A patent/JPS5851553B2/ja not_active Expired
1976
- 1976-09-17 GB GB3868376A patent/GB1543356A/en not_active Expired
- 1976-09-27 FR FR7629006A patent/FR2325698A1/fr active Granted
- 1976-09-28 BE BE170995A patent/BE846653A/fr unknown
- 1976-09-28 CH CH1225376A patent/CH624136A5/de not_active IP Right Cessation
- 1976-09-28 DE DE19762643673 patent/DE2643673A1/de not_active Withdrawn

Also Published As

Publication number	Publication date
DE2643673A1 (de)	1977-04-07
CH624136A5 (en)	1981-07-15
FR2325698B1 (fr)	1979-02-16
JPS5240687A (en)	1977-03-29
GB1543356A (en)	1979-04-04
FR2325698A1 (fr)	1977-04-22
BE846653A (fr)	1977-03-28

Publication	Publication Date	Title
JPH0748781A (ja)	1995-02-21	三色法でセルロース繊維材料を染色または捺染する方法
JPS5848672B2 (ja)	1983-10-29	セルロ−ズ系繊維の染色法
DE2557141A1 (de)	1976-07-01	Reaktivfarbstoffe, deren herstellung und verwendung
JPH0239545B2 (fr)	1990-09-06
JPS5838554B2 (ja)	1983-08-23	ホウコウゾクポリエステル／セルロ−スコウシヨクブツノレンゾクテキセンシヨクホウ
JPH0124826B2 (fr)	1989-05-15
JPS6067562A (ja)	1985-04-17	ホルマザン化合物及びこれを用いるセルロ−ス系繊維の染色法
CN101481537A (zh)	2009-07-15	具有n,n-二烷胺基桥基的新型反应性染料
JPS61247760A (ja)	1986-11-05	ヒドロキシ基を含有する繊維材料の染色又は捺染法
JPS6326149B2 (fr)	1988-05-28
KR100216860B1 (ko)	1999-09-01	반응성 염료
KR890001784B1 (ko)	1989-05-22	모노 아조화합물의 제조방법
JPH0247163A (ja)	1990-02-16	繊維反応性フオルマザン染料とその製造法及び使用法
JP2004124053A (ja)	2004-04-22	繊維反応性染料およびその製造方法
US3248379A (en)	1966-04-26	Fiber reactive dyestuffs and process for their preparation
JPS5851553B2 (ja)	1983-11-17	セルロ−スケイセンイノセンシヨクホウ
JPS591782A (ja)	1984-01-07	反応染料による織物繊維材料の染色または捺染方法
US3301846A (en)	1967-01-31	Dyestuffs containing chloromethyl or bromomethyl groups
US5928387A (en)	1999-07-27	Dye mixtures, process for their preparation and their use
US3042475A (en)	1962-07-03	New dyestuffs and process for colouring textile materials therewith
JPS6365712B2 (fr)	1988-12-16
JP2002532606A (ja)	2002-10-02	繊維反応性ジスアゾ染料
US3278515A (en)	1966-10-11	Organo azo, anthraquinone and phthalocyanine dyestuffs
JPS5857465B2 (ja)	1983-12-20	新規反応性アゾ染料、その製法及びそれによる染色法
JPS6136542B2 (fr)	1986-08-19