DE166903C - - Google Patents

Info

Publication number

DE166903C

DE166903C DE1904166903D DE166903DA DE166903C DE 166903 C DE166903 C DE 166903C DE 1904166903 D DE1904166903 D DE 1904166903D DE 166903D A DE166903D A DE 166903DA DE 166903 C DE166903 C DE 166903C

Authority

DE

Germany

Prior art keywords

red

bluish

amidonaphthol

yellowish

sulfonic acid

Prior art date

1904-06-01

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 - Lifetime

Links

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• DPMA
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• 239000002253 acid Substances 0.000 claims description 4
• 150000003460 sulfonic acids Chemical class 0.000 claims description 4
• 239000007859 condensation product Substances 0.000 claims description 3
• 150000008049 diazo compounds Chemical class 0.000 claims description 3
• 150000007513 acids Chemical class 0.000 claims description 2
• 239000003513 alkali Substances 0.000 claims description 2
• 150000003934 aromatic aldehydes Chemical class 0.000 claims description 2
• 229920001021 polysulfide Polymers 0.000 claims description 2
• 150000003557 thiazoles Chemical class 0.000 claims description 2
• 239000000987 azo dye Substances 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• 238000002360 preparation method Methods 0.000 claims 1
• 239000000975 dye Substances 0.000 description 9
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
• 229920000742 Cotton Polymers 0.000 description 5
• CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 4
• JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 4
• -1 benzylidene compound Chemical class 0.000 description 4
• NAYGOLGTZZLECJ-UHFFFAOYSA-N 1,3-thiazole-2-sulfonic acid Chemical class OS(=O)(=O)C1=NC=CS1 NAYGOLGTZZLECJ-UHFFFAOYSA-N 0.000 description 2
• CFWUNLOHNGQFAV-UHFFFAOYSA-N NC1=CC=CC=C1.CC1=CC=CC=C1N Chemical compound NC1=CC=CC=C1.CC1=CC=CC=C1N CFWUNLOHNGQFAV-UHFFFAOYSA-N 0.000 description 2
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
• 238000004040 coloring Methods 0.000 description 2
• VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 2
• CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 description 1
• YRHLHUWKALTDLY-UHFFFAOYSA-N 2-methoxyaniline;2-methylaniline Chemical compound CC1=CC=CC=C1N.COC1=CC=CC=C1N YRHLHUWKALTDLY-UHFFFAOYSA-N 0.000 description 1
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
• ZETIVVHRRQLWFW-UHFFFAOYSA-N 3-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1 ZETIVVHRRQLWFW-UHFFFAOYSA-N 0.000 description 1
• ZUJURJDZOPMJPH-UHFFFAOYSA-N 5-diazocyclohexa-1,3-diene;hydrochloride Chemical compound Cl.[N-]=[N+]=C1CC=CC=C1 ZUJURJDZOPMJPH-UHFFFAOYSA-N 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 230000003796 beauty Effects 0.000 description 1
• 230000008878 coupling Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 238000005859 coupling reaction Methods 0.000 description 1
• 239000000835 fiber Substances 0.000 description 1
• 238000005185 salting out Methods 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1