1327-79-3O=C1C=CC(=Nc2ccc3[nH]c4ccccc4c3c2)C=C1FMKXFJQAVQXMPX-UHFFFAOYSA-N1327-79-3、66104-61-8DTXSID4061674Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
This chemical does not meet GHS hazard criteria for 100% (10 of 10) of all reports.
Not Classified
Aggregated GHS information provided per 10 reports by companies from 1 notifications to the ECHA C&L Inventory.
Preparation3-(4-Hydroxyanilino)carbazole in 107 ℃ in Butanol sodium polysulfide solution reflux heating 24 hours, and then with sodium nitrite short time heating, steam out of Butanol, through the air and add salt to make dye completely precipitated out. This indophenol is by carbazole and nitroso phenol in concentrated sulfuric acid in – 20 to 23 ℃ condensation, then reduction and have to (BIOS983, 71 -74). To cure solution is to add 3 – methyl – 4 ‘- hydroxy – 4 -aminodiphenylamine, 4, 4’ – dihydroxydiphenyl aniline and phenol , improved the performance of the dye (BIOS983, 75- 81). Note: use with C.I. leuco sulfur dye similar method, some the structure of the dyes can be converted into the leuco compound.
No reaction records under the current filter.
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