2-nitrodiphenylamine

Also known as CI 10335, 2-nitro-N-phenylaniline

2-Nitrodiphenylamine is an organic chemical with the formula . It is a nitrated derivative of diphenylamine. It is a red solid, usually found in form of flakes or powder. It is polar but hydrophobic.

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Vinony's link graph records 9 inbound references to 2-nitrodiphenylamine, and connects out to mass density, digital object identifier and chemical formula.

Vinony files it under 2-Nitrophenyl compounds, Anilines and Chembox having GHS data.

Vinony links it to 7 Wikipedia language editions.

Chemical data

Formula: C12H10N2O2
Molecular weight: 214.22 g/mol
IUPAC name: 2-nitro-N-phenylaniline
SMILES: C1=CC=C(C=C1)NC2=CC=CC=C2[N+](=O)[O-]
InChIKey: RUKISNQKOIKZGT-UHFFFAOYSA-N
XLogP: 3.7
Polar surface area: 57.9 Å²
H-bond donors: 1
H-bond acceptors: 3
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of: chemical compound
Mass: 214.074228

Show 3 more facts

chemical formula: C₁₂H₁₀N₂O₂
canonical SMILES: C1=CC=C(C=C1)NC2=CC=CC=C2[N+](=O)[O-]
Commons category: 2-Nitrodiphenylamine

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Encyclopedic overview

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Contents

References
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2-Nitrodiphenylamine is an organic chemical with the formula . It is a nitrated derivative of diphenylamine. It is a red solid, usually found in form of flakes or powder. It is polar but hydrophobic.

Diphenylamine is used to extend the shelf-life of explosives containing nitrocellulose or nitroglycerin. Such nitrated materials release nitrogen oxides, which deteriorate the device. The diphenylamine traps NO2, affording the title compound and related species. And the title compound further traps additional nitrogen oxides. One of its major uses is to control the explosion rate of propylene glycol dinitrate.

Excerpted from Wikipedia’s “2-nitrodiphenylamine” article, available under the CC BY-SA 4.0 licence.