JPS6244585B2 - - Google Patents
Info
- Publication number
- JPS6244585B2 JPS6244585B2 JP54058736A JP5873679A JPS6244585B2 JP S6244585 B2 JPS6244585 B2 JP S6244585B2 JP 54058736 A JP54058736 A JP 54058736A JP 5873679 A JP5873679 A JP 5873679A JP S6244585 B2 JPS6244585 B2 JP S6244585B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- parts
- atoms
- dye
- formula
- Prior art date
- 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
Links
- 239000000975 dye Substances 0.000 claims description 55
- 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 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 20
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical group O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- -1 alkylene glycol Chemical compound 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 230000003165 hydrotropic effect Effects 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 7
- 239000004202 carbamide Substances 0.000 claims description 7
- 150000003863 ammonium salts Chemical class 0.000 claims description 6
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 5
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 5
- 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 claims description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052744 lithium Inorganic materials 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 150000001447 alkali salts Chemical class 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 239000003752 hydrotrope Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 238000004043 dyeing Methods 0.000 description 24
- 239000000243 solution Substances 0.000 description 20
- 238000005859 coupling reaction Methods 0.000 description 13
- 239000002253 acid Substances 0.000 description 12
- 230000008878 coupling Effects 0.000 description 10
- 238000010168 coupling process Methods 0.000 description 10
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 7
- 235000013877 carbamide Nutrition 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- XRTJYEIMLZALBD-UHFFFAOYSA-N 4-(6-methyl-1,3-benzothiazol-2-yl)aniline Chemical compound S1C2=CC(C)=CC=C2N=C1C1=CC=C(N)C=C1 XRTJYEIMLZALBD-UHFFFAOYSA-N 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
- 238000010186 staining Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- LDPKDIVFHXKSCE-PCVCHNHVSA-N (2S,3R,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aS,12aS,14aR,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxane-2-carboxylic acid Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](O[C@@H]2C([C@H]3[C@]([C@@H]4[C@@]([C@@]5(C[C@@H](O)[C@@]6(CO)CCC(C)(C)C[C@H]6C5=CC4)C)(C)CC3)(C)CC2)(C)C)O[C@H](C(O)=O)[C@H](O[C@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)O2)O)[C@@H]1O LDPKDIVFHXKSCE-PCVCHNHVSA-N 0.000 description 3
- KGZUHYIHYBDNLC-UHFFFAOYSA-N 2-(4-aminophenyl)-6-methyl-1,3-benzothiazole-7-sulfonic acid Chemical compound S1C2=C(S(O)(=O)=O)C(C)=CC=C2N=C1C1=CC=C(N)C=C1 KGZUHYIHYBDNLC-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000010985 leather Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 235000010288 sodium nitrite Nutrition 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 210000004243 sweat Anatomy 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- ULMIHUDGVZOBII-UHFFFAOYSA-N 4-(4,6-dimethyl-1,3-benzothiazol-2-yl)-2-methylaniline Chemical compound S1C2=CC(C)=CC(C)=C2N=C1C1=CC=C(N)C(C)=C1 ULMIHUDGVZOBII-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010014 continuous dyeing Methods 0.000 description 2
- 238000006193 diazotization reaction Methods 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 239000000982 direct dye Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229960004063 propylene glycol Drugs 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000010015 semi-continuous dyeing Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- 239000000979 synthetic dye Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- GDJZZWYLFXAGFH-UHFFFAOYSA-N 1,6-dimethylcyclohexa-2,4-diene-1-sulfonic acid Chemical compound CC1C=CC=CC1(C)S(O)(=O)=O GDJZZWYLFXAGFH-UHFFFAOYSA-N 0.000 description 1
- XAAHIQXKUAFJEI-UHFFFAOYSA-N 2,5-diethoxy-4-(3-oxobutanoylamino)benzenesulfonic acid Chemical compound CCOC1=CC(S(O)(=O)=O)=C(OCC)C=C1NC(=O)CC(C)=O XAAHIQXKUAFJEI-UHFFFAOYSA-N 0.000 description 1
- WTXXGGVYTMCHLV-UHFFFAOYSA-N 2,5-dimethoxy-4-(3-oxobutanoylamino)benzenesulfonic acid Chemical compound COC1=CC(S(O)(=O)=O)=C(OC)C=C1NC(=O)CC(C)=O WTXXGGVYTMCHLV-UHFFFAOYSA-N 0.000 description 1
- HWQJXEYYDDWZTP-UHFFFAOYSA-N 2-(4-amino-3-methylphenyl)-4,6-dimethyl-1,3-benzothiazole-7-sulfonic acid Chemical compound C1=C(N)C(C)=CC(C=2SC3=C(C(C)=CC(C)=C3N=2)S(O)(=O)=O)=C1 HWQJXEYYDDWZTP-UHFFFAOYSA-N 0.000 description 1
- ZDMLUAJVFNNSIX-UHFFFAOYSA-N 2-(4-aminophenyl)-6-methyl-1,3-benzothiazole-5-sulfonic acid Chemical compound N=1C=2C=C(S(O)(=O)=O)C(C)=CC=2SC=1C1=CC=C(N)C=C1 ZDMLUAJVFNNSIX-UHFFFAOYSA-N 0.000 description 1
- MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
- GHICZYPLGGUMOX-UHFFFAOYSA-N 2-amino-3-methoxy-6-methyl-4-(3-oxobutanoyl)benzenesulfonic acid Chemical compound COC1=C(N)C(S(O)(=O)=O)=C(C)C=C1C(=O)CC(C)=O GHICZYPLGGUMOX-UHFFFAOYSA-N 0.000 description 1
- XSWLKZZFJFSWDL-UHFFFAOYSA-N 5-ethoxy-2-methyl-4-(3-oxobutanoylamino)benzenesulfonic acid Chemical compound CCOC1=CC(S(O)(=O)=O)=C(C)C=C1NC(=O)CC(C)=O XSWLKZZFJFSWDL-UHFFFAOYSA-N 0.000 description 1
- YTSYXEDYBAQECZ-UHFFFAOYSA-N 5-methoxy-2-methyl-4-(3-oxobutanoylamino)benzenesulfonic acid Chemical compound COC1=CC(S(O)(=O)=O)=C(C)C=C1NC(=O)CC(C)=O YTSYXEDYBAQECZ-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 238000006887 Ullmann reaction Methods 0.000 description 1
- 235000013334 alcoholic beverage Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012431 aqueous reaction media Substances 0.000 description 1
- ZPDRZMNAFLBUOA-UHFFFAOYSA-N azane;5-methoxy-2-methyl-4-(3-oxobutanoylamino)benzenesulfonic acid Chemical compound [NH4+].COC1=CC(S([O-])(=O)=O)=C(C)C=C1NC(=O)CC(C)=O ZPDRZMNAFLBUOA-UHFFFAOYSA-N 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229940077386 sodium benzenesulfonate Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 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
- QSJBCWFEIGFVGB-UHFFFAOYSA-M sodium;4-(benzylamino)benzenesulfonate Chemical compound [Na+].C1=CC(S(=O)(=O)[O-])=CC=C1NCC1=CC=CC=C1 QSJBCWFEIGFVGB-UHFFFAOYSA-M 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000012192 staining solution Substances 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
- 239000012209 synthetic fiber Substances 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
- C09B29/0011—Monoazo dyes prepared by diazotising and coupling from diazotized anilines from diazotized anilines directly substituted by a heterocyclic ring (not condensed)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
- C07D277/66—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
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Claims (1)
- ãç¹èš±è«æ±ã®ç¯å²ã ïŒ æ¬¡åŒ ïŒåŒäžR1ïŒïŒãïŒåã®ïŒ£ååãæããã¢ã«ã
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éæ žåã³ïŒåã¯ã¯ïŒãïŒåã®ïŒ£ååãæãã
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ïŒã¡ãã«åã¯ïŒâã¡ãã«âïŒâã¹ã«ãâãã³ãºã
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ãŠã âããããªãŠã âåã³ïŒåã¯ã¢ã³ã¢ããŠã å¡©
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âãã³ãºãã¢ãŸãªãŒã«â(2)ãR2ïŒã¡ãã«ãã¡ã
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ïŒïŒåã¯ïŒãæå³ããæ žåã³ïŒåã¯ã¯æŽã«çœ®
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ã®ç¯å²ç¬¬ïŒé ã«ããã¢ãã¢ãŸææã ïŒ ã¢ããåã³ã¢ã«ã³ãŒã«ç³»ã®ãããããããŒå
åç©ïŒååã¯ãã以äžå«æããæ¿çž®æ°Žæ§æº¶æ¶²ãšã
ãŠååšãããç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé åã¯ç¬¬ïŒé ã«
ããã¢ãã¢ãŸææã ïŒ ãããããããŒå€ãšããŠå°¿çŽ åã³ïŒåã¯Îµâ
ã«ããã©ã¯ã¿ã åã³ïŒåã¯ã¢ã«ãã¬ã³æ®åºäžã«ïŒ
ãïŒåã®ïŒ£ååãæããã¢ã«ãã¬ã³ã°ãªã³ãŒã«ã
å«æããæ¿çž®æ°Žæ§æº¶æ¶²ãšããŠååšãããç¹èš±è«æ±
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æã
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782821350 DE2821350A1 (de) | 1978-05-16 | 1978-05-16 | Wasserloesliche monoazofarbstoffe, ihre herstellung, verwendung und damit gefaerbte und bedruckte materialien |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54155223A JPS54155223A (en) | 1979-12-07 |
| JPS6244585B2 true JPS6244585B2 (ja) | 1987-09-21 |
Family
ID=6039488
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5873679A Granted JPS54155223A (en) | 1978-05-16 | 1979-05-15 | Water soluble monoazo dye*preparation and application thereof |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4254026A (ja) |
| EP (1) | EP0005449B1 (ja) |
| JP (1) | JPS54155223A (ja) |
| BR (1) | BR7902974A (ja) |
| CA (1) | CA1109062A (ja) |
| DE (2) | DE2821350A1 (ja) |
| IN (1) | IN151131B (ja) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0242331B1 (de) * | 1986-04-16 | 1992-12-30 | Ciba-Geigy Ag | Azofarbstoffe |
| DE3735078A1 (de) * | 1987-10-16 | 1989-04-27 | Cassella Ag | Wasserloesliche gelbe monoazofarbstoffe |
| BRPI0811925B1 (pt) * | 2007-05-23 | 2017-12-12 | Archroma Ip Gmbh | Concentrated aqueous solutions, its use, ink cartridges, and substrates composing hydroxyl |
| JP2012067168A (ja) * | 2010-09-22 | 2012-04-05 | Mitsubishi Chemicals Corp | æ·»å å€ãé¡æåæ£æ¶²ãã«ã©ãŒãã£ã«ã¿çšçè²æš¹èçµæç©ãã«ã©ãŒãã£ã«ã¿ã液æ¶è¡šç€ºè£ 眮åã³ææ©ïœ ïœè¡šç€ºè£ 眮 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1833269A (en) * | 1927-01-26 | 1931-11-24 | Gen Aniline Works Inc | New azo dye |
| GB310354A (en) * | 1928-01-24 | 1929-04-24 | Ig Farbenindustrie Ag | Process for the manufacture of cotton dyestuffs |
| US2283823A (en) * | 1939-11-07 | 1942-05-19 | Gen Aniline & Film Corp | Monoazo dyestuffs soluble in water |
| US2657202A (en) * | 1948-04-16 | 1953-10-27 | Ciba Ltd | Azo dyestuffs |
| US3274171A (en) | 1963-04-29 | 1966-09-20 | Allied Chem | Monoazo dyestuffs containing a benzothiazole nucleus |
| DE1932246U (de) | 1965-11-10 | 1966-02-10 | Josef Rebele | Beton-formstein, insbesondere fuer die befestigung von boeschungen, fahrbahnen usw. |
| FR1600819A (ja) * | 1968-06-26 | 1970-08-03 | ||
| CH554397A (de) * | 1971-02-16 | 1974-09-30 | Sandoz Ag | Verfahren zur herstellung von azofarbstoffen. |
-
1978
- 1978-05-16 DE DE19782821350 patent/DE2821350A1/de not_active Withdrawn
-
1979
- 1979-03-19 US US06/021,465 patent/US4254026A/en not_active Expired - Lifetime
- 1979-03-23 IN IN279/CAL/79A patent/IN151131B/en unknown
- 1979-04-09 EP EP79101088A patent/EP0005449B1/de not_active Expired
- 1979-04-09 DE DE7979101088T patent/DE2961742D1/de not_active Expired
- 1979-05-15 JP JP5873679A patent/JPS54155223A/ja active Granted
- 1979-05-15 BR BR7902974A patent/BR7902974A/pt unknown
- 1979-05-15 CA CA327,636A patent/CA1109062A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IN151131B (ja) | 1983-02-26 |
| CA1109062A (en) | 1981-09-15 |
| DE2821350A1 (de) | 1979-11-22 |
| JPS54155223A (en) | 1979-12-07 |
| BR7902974A (pt) | 1979-11-27 |
| US4254026A (en) | 1981-03-03 |
| EP0005449B1 (de) | 1982-01-06 |
| DE2961742D1 (en) | 1982-02-25 |
| EP0005449A1 (de) | 1979-11-28 |
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