Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Vinony's link graph records 5 inbound references to Disperse Orange 1, and connects out to digital object identifier, chemical formula and melting point.
Vinony files it under 4-Nitrophenyl compounds, Anilines and Azo dyes.
Vinony links it to 5 Wikipedia language editions.
Chemical data
- Formula
- C18H14N4O2
- Molecular weight
- 318.3 g/mol
- IUPAC name
- 4-[(4-nitrophenyl)diazenyl]-N-phenylaniline
- SMILES
- C1=CC=C(C=C1)NC2=CC=C(C=C2)N=NC3=CC=C(C=C3)[N+](=O)[O-]
- InChIKey
- YFVXLROHJBSEDW-UHFFFAOYSA-N
- XLogP
- 5.5
- Polar surface area
- 82.6 Ų
- H-bond donors
- 1
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Research
26 papers- Sensitizing capacity of Disperse Orange 1 and its potential metabolites from azo reduction and their cross-reactivity pattern.Contact dermatitis · 2013
- Exclusion of Disperse Orange 3 is possible from the textile dye mix present in the Swedish baseline patch test series. A study by the Swedish Contact Dermatitis Research Group.Contact dermatitis · 2023
- The azo dyes Disperse Red 1 and Disperse Orange 1 increase the micronuclei frequencies in human lymphocytes and in HepG2 cells.Mutation research · 2009
- Patch testing with the textile dyes Disperse Orange 1 and Disperse Yellow 3 and some of their potential metabolites, and simultaneous reactions to para-amino compounds.Contact dermatitis · 2012
- Chlorination treatment of aqueous samples reduces, but does not eliminate, the mutagenic effect of the azo dyes Disperse Red 1, Disperse Red 13 and Disperse Orange 1.Mutation research · 2010
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 318.111664
- Has use
- dye
Show 3 more facts
- chemical formula
- C₁₈H₁₄N₄O₂
- canonical SMILES
- C1=CC=C(C=C1)NC2=CC=C(C=C2)N=NC3=CC=C(C=C3)[N+](=O)[O-]
- isomeric SMILES
- C1=CC=C(C=C1)NC2=CC=C(C=C2)/N=N/C3=CC=C(C=C3)[N+](=O)[O-]
Sources (2)
via Wikidata · CC0
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