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Phenol, 4-(9H-carbazol-3-ylamino)-

HCID 6852
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Basic information

CAS
86-72-6
Standard SMILES
Oc1ccc(Nc2ccc3[nH]c4ccccc4c3c2)cc1
InChIKey
STRAHSCTRLRZNU-UHFFFAOYSA-N
Molecular formula
C18H14N2O
Average molar mass
274.3 g/mol
Monoisotopic mass
274.11061307

Names & identifiers

Preferred name
Phenol, 4-(9H-carbazol-3-ylamino)-
IUPAC
4-(9H-carbazol-3-ylamino)phenol
English name
4-(3-CARBAZOLYLAMINO)PHENOL
Molecular formula
C18H14N2O
Molecular weight
274.32

Names & synonyms

4-(9H-Carbazol-3-ylamino)phenol86-72-6Phenol, 4-(9H-carbazol-3-ylamino)-Hydron Blue 3RNHidrotin Blue 2RHidrotin Blue 3R4-(3-Carbazolylamino)phenolr-BaseC.I. Vat Blue 47R-Base [Czech]Phenol, 4-(3-carbazolylamino)-Carbazole, 3-(p-hydroxyanilino)-
Show more names
Vat blue 47Carbazolindophenol3-(4-hydroxyanilino)carbazolePhenol, 4-(9H-Carbazol-3-Yl-Amino)-
3-(4'-Hydroxyfenyl)aminokarbazolEINECS 201-693-4NSC 75903BRN 02474813-(4'-Hydroxyfenyl)aminokarbazol [Czech]DTXSID90589474-22-00-04937 (Beilstein Handbook Reference)RefChem:172806

Database identifiers

CAS
86-72-6
PubChem CID
6852
DTXSID
DTXSID9058947
UNII
CDU7Q26X7S
EC Number
201-693-4
Nikkaji
J10.133H

Properties

Computed structural propertiesFilling in

XLogP
4.9
Topological polar surface area
48.1 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
2
Rotatable bonds
2
Heavy atoms
21
Formal charge
0
Complexity
353

Physicochemical properties

Boiling point
417.3 °C · 417.3°C (rough estimate)
Density
1.153 · 1.1530 (rough estimate)
refractive index
1.58 · 1.5800 (estimate)
pka
10.81 · 10.81±0.26(Predicted)
CAS DataBase Reference
86 · 86-72-6
EPA Substance Registry System
4 · Phenol, 4-(9H-carbazol-3-ylamino)- (86-72-6)
TSCA
TSCA listed

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

tsca
TSCA listed

Chemistry & industry

Applications · 1 item

Uses4-(9H-Carbazol-3-ylamino)phenol is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells.

Preparation methods · 1 item

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.

Upstream & downstream products

Upstream raw materials

4-(3-CARBAZOLYLAMINO)PHENOL

Downstream products

4-(3-CARBAZOLYLAMINO)PHENOLVat Blue 43Phenol, 4-(9H-carbazol-3-ylamino)-, reaction products with 4-(2-naphthalenylamino)phenol, 4-nitrophenol and sodium sulfide (Na2(Sx)), oxidized

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Compound notes

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Suppliers3 total

TargetMol 中国(陶术生物)400-821-0310 15002144251 · [email protected]
Alfa Chemistry+1-5166625404 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]