JPS62172065A - 塩基性アゾ染料の濃厚な貯蔵安定性溶液 - Google Patents

塩基性アゾ染料の濃厚な貯蔵安定性溶液

Info

Publication number: JPS62172065A
Authority: JP; Japan
Prior art keywords: dye; water; basic; parts; primary amino
Prior art date: 1986-01-23
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.): Granted

Application number

JP1255286A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0154375B2 (fr

Inventor

Nobuaki Takagaki

高垣　信明

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.)

Individual

Original Assignee

Individual

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.)

1986-01-23

Filing date

1986-01-23

Publication date

1987-07-29

1986-01-23 Application filed by Individual filed Critical Individual

1986-01-23 Priority to JP1255286A priority Critical patent/JPS62172065A/ja

1987-07-29 Publication of JPS62172065A publication Critical patent/JPS62172065A/ja

1989-11-17 Publication of JPH0154375B2 publication Critical patent/JPH0154375B2/ja

Status Granted legal-status Critical Current

Links

239000000987 azo dye Substances 0.000 title description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
239000000981 basic dye Substances 0.000 claims abstract description 18
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 8
239000012190 activator Substances 0.000 claims abstract description 4
239000000243 solution Substances 0.000 claims description 11
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 5
239000007864 aqueous solution Substances 0.000 claims description 2
239000000975 dye Substances 0.000 abstract description 34
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract description 7
239000000843 powder Substances 0.000 abstract description 4
IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 abstract 2
150000003973 alkyl amines Chemical class 0.000 abstract 1
230000007797 corrosion Effects 0.000 abstract 1
238000005260 corrosion Methods 0.000 abstract 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
238000000034 method Methods 0.000 description 13
239000007788 liquid Substances 0.000 description 11
238000004043 dyeing Methods 0.000 description 7
LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 7
239000002904 solvent Substances 0.000 description 6
239000002253 acid Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
239000000203 mixture Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
WLKAMFOFXYCYDK-UHFFFAOYSA-N [5-amino-4-[[3-[(2-amino-4-azaniumyl-5-methylphenyl)diazenyl]-4-methylphenyl]diazenyl]-2-methylphenyl]azanium;dichloride Chemical compound [Cl-].[Cl-].CC1=CC=C(N=NC=2C(=CC([NH3+])=C(C)C=2)N)C=C1N=NC1=CC(C)=C([NH3+])C=C1N WLKAMFOFXYCYDK-UHFFFAOYSA-N 0.000 description 3
238000004040 coloring Methods 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
235000011114 ammonium hydroxide Nutrition 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
239000012535 impurity Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
239000004317 sodium nitrate Substances 0.000 description 2
235000010344 sodium nitrate Nutrition 0.000 description 2
238000010186 staining Methods 0.000 description 2
WKVZMKDXJFCMMD-UVWUDEKDSA-L (5ar,8ar,9r)-5-[[(2r,4ar,6r,7r,8r,8as)-7,8-dihydroxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5h-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one;azanide;n,3-bis(2-chloroethyl)-2-ox Chemical compound [NH2-].[NH2-].Cl[Pt+2]Cl.ClCCNP1(=O)OCCCN1CCCl.COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3C(O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 WKVZMKDXJFCMMD-UVWUDEKDSA-L 0.000 description 1
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
MCZVRBLCRZWFJH-UHFFFAOYSA-N Bismark brown Y Chemical compound Cl.Cl.NC1=CC(N)=CC=C1N=NC1=CC=CC(N=NC=2C(=CC(N)=CC=2)N)=C1 MCZVRBLCRZWFJH-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
239000003125 aqueous solvent Substances 0.000 description 1
239000012752 auxiliary agent Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000012263 liquid product 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
-1 organic acid salt Chemical class 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000007639 printing Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
NFBOTFJHZAHUJK-UHFFFAOYSA-N sulfamic acid;toluene Chemical compound NS(O)(=O)=O.CC1=CC=CC=C1 NFBOTFJHZAHUJK-UHFFFAOYSA-N 0.000 description 1
FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical class NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
239000002023 wood Substances 0.000 description 1

Landscapes

Cosmetics (AREA)
Coloring (AREA)

JP1255286A 1986-01-23 1986-01-23 塩基性アゾ染料の濃厚な貯蔵安定性溶液 Granted JPS62172065A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1255286A JPS62172065A (ja)	1986-01-23	1986-01-23	塩基性アゾ染料の濃厚な貯蔵安定性溶液

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1255286A JPS62172065A (ja)	1986-01-23	1986-01-23	塩基性アゾ染料の濃厚な貯蔵安定性溶液

Publications (2)

Publication Number	Publication Date
JPS62172065A true JPS62172065A (ja)	1987-07-29
JPH0154375B2 JPH0154375B2 (fr)	1989-11-17

Family

ID=11808497

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1255286A Granted JPS62172065A (ja)	1986-01-23	1986-01-23	塩基性アゾ染料の濃厚な貯蔵安定性溶液

Country Status (1)

Country	Link
JP (1)	JPS62172065A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH07307581A (ja) *	1994-05-13	1995-11-21	Nec Corp	屋外筐体

1986
- 1986-01-23 JP JP1255286A patent/JPS62172065A/ja active Granted

Also Published As

Publication number	Publication date
JPH0154375B2 (fr)	1989-11-17

Publication	Publication Date	Title
US6860906B2 (en)	2005-03-01	Process for preparing solutions of anionic organic compounds
JPH0523306B2 (fr)	1993-04-02
JPS588765A (ja)	1983-01-18	反応染料−液体配合物及びその使用法
US3963418A (en)	1976-06-15	Yellow disazo acid dye solution
US6585782B2 (en)	2003-07-01	Mixtures of reactive dyes and their use
JPH0579705B2 (fr)	1993-11-04
US3681320A (en)	1972-08-01	Preparation of disazo j acid urea dyestuffs
JPS62246968A (ja)	1987-10-28	反応染料液状組成物
US6719906B1 (en)	2004-04-13	Process for the preparation of solutions of anionic organic compounds
JPS58187460A (ja)	1983-11-01	低温染色性繊維反応性染料の濃厚流動性配合物
JPS62172065A (ja)	1987-07-29	塩基性アゾ染料の濃厚な貯蔵安定性溶液
JPS63178169A (ja)	1988-07-22	ジスアゾ顔料組成物
US4002424A (en)	1977-01-11	Solution of isomer mixture of naphthylazophenylazonaphthyl disulfonate dye
GB1569259A (en)	1980-06-11	Concentrated aqueous solutions of disazo dyes
TW201802B (fr)	1993-03-11
US20080201872A1 (en)	2008-08-28	Aqueous Formulations Of Dye Mixtures
JP2552732B2 (ja)	1996-11-13	トリスアゾ染料と紙の染色方法
US2263616A (en)	1941-11-25	Composition comprising ice color coupling components
US4654045A (en)	1987-03-31	Process for preparation of concentrated anionic red dye solutions
US4426205A (en)	1984-01-17	Novel red dyes for fiberglass and paper
CA1073611A (fr)	1980-03-18	Teintures, et procede de production
JPS6211774A (ja)	1987-01-20	液体染料組成物
JPH05222315A (ja)	1993-08-31	流動性の染料製剤
JPS6218472A (ja)	1987-01-27	インキ組成物
JPS58125758A (ja)	1983-07-26	アニオン性染料組成物