DE107626A - - Google Patents

Info

Publication number

DE107626A

DE107626A DE107626A DE 107626 A DE107626 A DE 107626A DE 107626 A DE107626 A DE 107626A

Authority

DE

Germany

Prior art keywords

toluidine

amidobenzyl

formaldehyde

xylidine

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.)

Pending

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• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 21
• 239000007859 condensation product Substances 0.000 claims description 4
• 238000000034 method Methods 0.000 claims description 4
• 239000007800 oxidant agent Substances 0.000 claims description 4
• WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 3
• CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 claims description 3
• 229940018564 m-phenylenediamine Drugs 0.000 claims description 3
• VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 claims description 2
• 239000000999 acridine dye Substances 0.000 claims description 2
• 238000002360 preparation method Methods 0.000 claims description 2
• 239000000975 dye Substances 0.000 description 16
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
• 229910021529 ammonia Inorganic materials 0.000 description 5
• 230000015572 biosynthetic process Effects 0.000 description 5
• 230000008030 elimination Effects 0.000 description 3
• 238000003379 elimination reaction Methods 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• UXJHQQLYKUVLIE-UHFFFAOYSA-N 1,2-dihydroacridine Chemical class C1=CC=C2N=C(C=CCC3)C3=CC2=C1 UXJHQQLYKUVLIE-UHFFFAOYSA-N 0.000 description 2
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
• 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 150000004985 diamines Chemical class 0.000 description 2
• RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
• 239000000155 melt Substances 0.000 description 2
• LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
• 230000003647 oxidation Effects 0.000 description 2
• 238000007254 oxidation reaction Methods 0.000 description 2
• 239000002244 precipitate Substances 0.000 description 2
• UAJWDYLSRSNGFH-UHFFFAOYSA-N 1,3,5-tris(4-methylphenyl)-1,3,5-triazinane Chemical compound C1=CC(C)=CC=C1N1CN(C=2C=CC(C)=CC=2)CN(C=2C=CC(C)=CC=2)C1 UAJWDYLSRSNGFH-UHFFFAOYSA-N 0.000 description 1
• 229920000742 Cotton Polymers 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
• PLQKJDBVGPLFJP-UHFFFAOYSA-N OCl.NC1=CC(N)=CC=C1 Chemical compound OCl.NC1=CC(N)=CC=C1 PLQKJDBVGPLFJP-UHFFFAOYSA-N 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
• 238000003776 cleavage reaction Methods 0.000 description 1
• 238000004040 coloring Methods 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000004043 dyeing Methods 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 239000010985 leather Substances 0.000 description 1
• 238000002844 melting Methods 0.000 description 1
• 230000008018 melting Effects 0.000 description 1
• 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 description 1
• 229910052760 oxygen Inorganic materials 0.000 description 1
• 239000001301 oxygen Substances 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 230000007017 scission Effects 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 235000018553 tannin Nutrition 0.000 description 1
• 229920001864 tannin Polymers 0.000 description 1
• 239000001648 tannin Substances 0.000 description 1
• UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
• 238000010626 work up procedure Methods 0.000 description 1