DE121610C - - Google Patents

Info

Publication number

DE121610C

DE121610C DENDAT121610D DE121610DA DE121610C DE 121610 C DE121610 C DE 121610C DE NDAT121610 D DENDAT121610 D DE NDAT121610D DE 121610D A DE121610D A DE 121610DA DE 121610 C DE121610 C DE 121610C

Authority

DE

Germany

Prior art keywords

amidophenol

nitrosodialkyl

chlorohydrate

phenols

dyes

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.)

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• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 13
• 239000000975 dye Substances 0.000 claims description 11
• 150000002989 phenols Chemical class 0.000 claims description 6
• 238000000034 method Methods 0.000 claims description 4
• 150000001555 benzenes Chemical class 0.000 claims description 3
• -1 amine salts Chemical class 0.000 claims description 2
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
• 238000004040 coloring Methods 0.000 claims description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
• 230000007717 exclusion Effects 0.000 claims 1
• 238000010438 heat treatment Methods 0.000 claims 1
• 238000002360 preparation method Methods 0.000 claims 1
• 150000001412 amines Chemical class 0.000 description 5
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
• 229960000583 acetic acid Drugs 0.000 description 4
• WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 4
• YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
• 230000015572 biosynthetic process Effects 0.000 description 3
• 210000002268 wool Anatomy 0.000 description 3
• BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 2
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
• VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
• JBCSOBKDUKAJHR-UHFFFAOYSA-N ClO.NC1=CC=CC=C1 Chemical compound ClO.NC1=CC=CC=C1 JBCSOBKDUKAJHR-UHFFFAOYSA-N 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 239000012362 glacial acetic acid Substances 0.000 description 2
• 239000001046 green dye Substances 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• 229940079877 pyrogallol Drugs 0.000 description 2
• 229960004889 salicylic acid Drugs 0.000 description 2
• 150000003839 salts Chemical class 0.000 description 2
• ORFSSYGWXNGVFB-UHFFFAOYSA-N sodium 4-amino-6-[[4-[4-[(8-amino-1-hydroxy-5,7-disulfonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-5-hydroxynaphthalene-1,3-disulfonic acid Chemical compound COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N=NC3=C(C4=C(C=C3)C(=CC(=C4N)S(=O)(=O)O)S(=O)(=O)O)O)OC)N=NC5=C(C6=C(C=C5)C(=CC(=C6N)S(=O)(=O)O)S(=O)(=O)O)O.[Na+] ORFSSYGWXNGVFB-UHFFFAOYSA-N 0.000 description 2
• YSVBPNGJESBVRM-ZPZFBZIMSA-L Carmoisine Chemical compound [Na+].[Na+].C1=CC=C2C(/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)O)=CC=C(S([O-])(=O)=O)C2=C1 YSVBPNGJESBVRM-ZPZFBZIMSA-L 0.000 description 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
• 229920000742 Cotton Polymers 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 229940039407 aniline Drugs 0.000 description 1
• 239000004176 azorubin Substances 0.000 description 1
• 235000012733 azorubine Nutrition 0.000 description 1
• 239000001045 blue dye Substances 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 229940031019 carmoisine Drugs 0.000 description 1
• 229910052801 chlorine Inorganic materials 0.000 description 1
• 239000000460 chlorine Substances 0.000 description 1
• 239000007859 condensation product Substances 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 238000006386 neutralization reaction Methods 0.000 description 1
• 150000004893 oxazines Chemical class 0.000 description 1
• 238000010186 staining Methods 0.000 description 1
• 125000001424 substituent group Chemical group 0.000 description 1