DE79972C - - Google Patents

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Publication number

DE79972C

DE79972C DENDAT79972D DE79972DA DE79972C DE 79972 C DE79972 C DE 79972C DE NDAT79972 D DENDAT79972 D DE NDAT79972D DE 79972D A DE79972D A DE 79972DA DE 79972 C DE79972 C DE 79972C

Authority

DE

Germany

Prior art keywords

monoethyl

phenylenediamine

homologues

monomethyl

toluenediamine

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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• 238000000034 method Methods 0.000 claims description 9
• ZMWAXVAETNTVAT-UHFFFAOYSA-N 7-n,8-n,5-triphenylphenazin-5-ium-2,3,7,8-tetramine;chloride Chemical compound [Cl-].C=1C=CC=CC=1NC=1C=C2[N+](C=3C=CC=CC=3)=C3C=C(N)C(N)=CC3=NC2=CC=1NC1=CC=CC=C1 ZMWAXVAETNTVAT-UHFFFAOYSA-N 0.000 claims description 4
• FRPAGJPHUNNVLJ-UHFFFAOYSA-N 2-n-ethylbenzene-1,2-diamine Chemical compound CCNC1=CC=CC=C1N FRPAGJPHUNNVLJ-UHFFFAOYSA-N 0.000 claims description 3
• 239000002253 acid Substances 0.000 claims description 3
• 238000002360 preparation method Methods 0.000 claims description 3
• HJSUAIIUCAMPJQ-UHFFFAOYSA-N 1-propylcyclohexa-3,5-diene-1,2-diamine Chemical compound CCCC1(N)C=CC=CC1N HJSUAIIUCAMPJQ-UHFFFAOYSA-N 0.000 claims description 2
• 150000004987 o-phenylenediamines Chemical class 0.000 claims description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
• BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims 1
• 239000000975 dye Substances 0.000 description 5
• 125000000217 alkyl group Chemical group 0.000 description 3
• 238000009833 condensation Methods 0.000 description 3
• 230000005494 condensation Effects 0.000 description 3
• GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 2
• XKBQWBOFFVJBHI-UHFFFAOYSA-N 1-ethylcyclohexa-3,5-diene-1,2-diamine Chemical compound CCC1(N)C=CC=CC1N XKBQWBOFFVJBHI-UHFFFAOYSA-N 0.000 description 2
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
• 150000003460 sulfonic acids Chemical class 0.000 description 2
• ZMBQZWCDYKGVLW-UHFFFAOYSA-N 1-methylcyclohexa-3,5-diene-1,2-diamine Chemical class CC1(N)C=CC=CC1N ZMBQZWCDYKGVLW-UHFFFAOYSA-N 0.000 description 1
• AZLFTFIVWFCCLK-UHFFFAOYSA-N 2-N,1-dimethylcyclohexa-3,5-diene-1,2-diamine Chemical compound CC1(C(C=CC=C1)NC)N AZLFTFIVWFCCLK-UHFFFAOYSA-N 0.000 description 1
• RPKCLSMBVQLWIN-UHFFFAOYSA-N 2-n-methylbenzene-1,2-diamine Chemical compound CNC1=CC=CC=C1N RPKCLSMBVQLWIN-UHFFFAOYSA-N 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
• KHXPJROZVKFBQV-UHFFFAOYSA-N C(C)NC1C(C)(C=CC=C1)N Chemical compound C(C)NC1C(C)(C=CC=C1)N KHXPJROZVKFBQV-UHFFFAOYSA-N 0.000 description 1
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 239000004922 lacquer Substances 0.000 description 1
• 229910052757 nitrogen Inorganic materials 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
• 239000002966 varnish Substances 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1