JPS58101154A

JPS58101154A - 合成繊維用モノアゾ染料

合成繊維用モノアゾ染料

Info

Publication number: JPS58101154A
Authority: JP; Japan
Prior art keywords: polyester; dye; dyeing; group; aniline
Prior art date: 1981-12-09
Legal status : Granted

Application number

JP19801281A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0116271B2 (enrdf_load_stackoverflow

Inventor

Toshio Niwa

俊夫丹羽

Kiyoshi Himeno

清姫野

Hiroshi Takimoto

滝本　浩

Current Assignee

GOSEI SENRIYOU GIJUTSU KENKYU KUMIAI

Original Assignee

GOSEI SENRIYOU GIJUTSU KENKYU KUMIAI

Priority date

1981-12-09

Filing date

1981-12-09

Publication date

1983-06-16

1981-12-09 Application filed by GOSEI SENRIYOU GIJUTSU KENKYU KUMIAI filed Critical GOSEI SENRIYOU GIJUTSU KENKYU KUMIAI

1981-12-09 Priority to JP19801281A priority Critical patent/JPS58101154A/ja

1983-06-16 Publication of JPS58101154A publication Critical patent/JPS58101154A/ja

1989-03-23 Publication of JPH0116271B2 publication Critical patent/JPH0116271B2/ja

Status Granted legal-status Critical Current

Links

229920002994 synthetic fiber Polymers 0.000 title claims description 8
239000012209 synthetic fiber Substances 0.000 title claims description 8
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 title claims description 7
-1 tetrahydrofurfuryl Chemical group 0.000 claims abstract description 12
229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
239000000975 dye Substances 0.000 claims description 16
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
238000004043 dyeing Methods 0.000 abstract description 15
229920000728 polyester Polymers 0.000 abstract description 12
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract description 6
230000008878 coupling Effects 0.000 abstract description 5
238000010168 coupling process Methods 0.000 abstract description 5
238000005859 coupling reaction Methods 0.000 abstract description 5
238000000859 sublimation Methods 0.000 abstract description 4
230000008022 sublimation Effects 0.000 abstract description 4
238000000034 method Methods 0.000 abstract description 3
239000003513 alkali Substances 0.000 abstract description 2
239000012954 diazonium Substances 0.000 abstract description 2
150000001989 diazonium salts Chemical class 0.000 abstract description 2
239000004814 polyurethane Substances 0.000 abstract description 2
229920002635 polyurethane Polymers 0.000 abstract description 2
238000012805 post-processing Methods 0.000 abstract description 2
239000000463 material Substances 0.000 abstract 2
DZRZHFOFVWAKGT-UHFFFAOYSA-N 3,5-dinitrothiophen-2-amine Chemical compound NC=1SC([N+]([O-])=O)=CC=1[N+]([O-])=O DZRZHFOFVWAKGT-UHFFFAOYSA-N 0.000 abstract 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
229920002301 cellulose acetate Polymers 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
238000007598 dipping method Methods 0.000 abstract 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
229920000139 polyethylene terephthalate Polymers 0.000 abstract 1
239000005020 polyethylene terephthalate Substances 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
239000004753 textile Substances 0.000 abstract 1
239000000835 fiber Substances 0.000 description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
239000004744 fabric Substances 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
238000007796 conventional method Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000000126 substance Substances 0.000 description 3
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
239000000987 azo dye Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
235000019253 formic acid Nutrition 0.000 description 2
239000000203 mixture Substances 0.000 description 2
229920001059 synthetic polymer Polymers 0.000 description 2
238000005406 washing Methods 0.000 description 2
KSYSOIGKYYSWBD-UHFFFAOYSA-N 2,3-dinitrothiophene Chemical compound [O-][N+](=O)C=1C=CSC=1[N+]([O-])=O KSYSOIGKYYSWBD-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
150000004992 toluidines Chemical class 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1