JPS57109860A

JPS57109860A - Disazo dye for polyester fiber

Disazo dye for polyester fiber

Info

Publication number: JPS57109860A
Authority: JP; Japan
Prior art keywords: formula; compound; polyester fiber; disazo dye; dyeing
Prior art date: 1980-12-26
Legal status : Granted

Application number

JP55189018A

Other languages

English (en)

Japanese (ja)

Other versions

JPS645069B2 (enrdf_load_stackoverflow

Inventor

Seiichi Imahori

Kiyoshi Himeno

Shuichi Maeda

Current Assignee

Mitsubishi Chemical Corp

Original Assignee

Mitsubishi Chemical Industries Ltd

Priority date

1980-12-26

Filing date

1980-12-26

Publication date

1982-07-08

1980-12-26 Application filed by Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd

1980-12-26 Priority to JP55189018A priority Critical patent/JPS57109860A/ja

1981-12-15 Priority to GB8137778A priority patent/GB2093056B/en

1981-12-23 Priority to DE19813151114 priority patent/DE3151114A1/de

1981-12-23 Priority to CH8258/81A priority patent/CH647254A5/de

1981-12-23 Priority to US06/334,005 priority patent/US4621136A/en

1982-07-08 Publication of JPS57109860A publication Critical patent/JPS57109860A/ja

1989-01-27 Publication of JPS645069B2 publication Critical patent/JPS645069B2/ja

Status Granted legal-status Critical Current

Links

125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title abstract 2
239000000835 fiber Substances 0.000 title abstract 2
229920000728 polyester Polymers 0.000 title abstract 2
125000003342 alkenyl group Chemical group 0.000 abstract 2
230000008878 coupling Effects 0.000 abstract 2
238000010168 coupling process Methods 0.000 abstract 2
238000005859 coupling reaction Methods 0.000 abstract 2
238000004043 dyeing Methods 0.000 abstract 2
-1 monoazo compound Chemical class 0.000 abstract 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
150000001412 amines Chemical class 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
239000004744 fabric Substances 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
239000000463 material Substances 0.000 abstract 1
238000000034 method Methods 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
125000005429 oxyalkyl group Chemical group 0.000 abstract 1
238000000859 sublimation Methods 0.000 abstract 1
230000008022 sublimation Effects 0.000 abstract 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical compound NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 abstract 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1