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103578

Sigma-Aldrich

4-Nitrodiphenylamin

99%

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About This Item

Lineare Formel:
C6H5NHC6H4NO2
CAS-Nummer:
836-30-6
Molekulargewicht:
214.22
EG-Nummer:
212-646-2
MDL-Nummer:
MFCD00007301
UNSPSC-Code:
12352100
eCl@ss:
39032032
PubChem Substanz-ID:
24846611
NACRES:
NA.22

Assay

99%

Form

solid

mp (Schmelzpunkt)

132-135 °C (lit.)

SMILES String

[O-][N+](=O)c1ccc(Nc2ccccc2)cc1

InChI

1S/C12H10N2O2/c15-14(16)12-8-6-11(7-9-12)13-10-4-2-1-3-5-10/h1-9,13H

InChIKey

XXYMSQQCBUKFHE-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

4-Nitrodiphenylamine undergoes heterogeneous catalytic transfer hydrogenation to form p-phenylenediamines. 4-Nitrodiphenylamine is used as stabilizer for propellants and explosives.

Anwendung

4-Nitrodiphenylamine was used to study reduction of nitrated diphenylamine derivatives in sediment water batch enrichments and dense cell suspensions of anaerobic, aromatic-compound-mineralizing pure bacterial cultures.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Heterogeneous catalytic transfer hydrogenation of 4-nitrodiphenylamine to p-phenylenediamines.
Banerjee AA and Mukesh D.
Journal of the Chemical Society. Chemical Communications, 18, 1275-1276 (1988)
Anne-Laure Gassner et al.
Science & justice : journal of the Forensic Science Society, 60(2), 136-144 (2020-03-01)
The present study investigated the organic gunshot residue (OGSR) background level of police vehicles in Switzerland. Specimens from 64 vehicles belonging to two regional police services were collected and analysed by LC-MS in positive mode. The driver's and back seats
O Drzyzga et al.
Applied and environmental microbiology, 61(9), 3282-3287 (1995-09-01)
2-Nitrodiphenylamine, 4-nitrodiphenylamine, and 2,4-dinitrodiphenylamine were anaerobically metabolized in sediment-water batch enrichments inoculated with mud from the German North Sea coast. The first intermediate in 2,4-dinitrodiphenylamine degradation was 2-amino-4-nitrodiphenylamine, which appeared in large (nearly stoichiometric) amounts before being completely reduced to
Anne-Laure Gassner et al.
Science & justice : journal of the Forensic Science Society, 59(1), 58-66 (2019-01-19)
The present study aimed at providing data to assess the secondary transfer of organic gunshot residues (OGSR). Three scenarios were evaluated in controlled conditions, namely displacing a firearm from point A to point B, a simple handshake and an arrest
Zuriñe Abrego et al.
The Analyst, 139(23), 6232-6241 (2014-10-11)
A method based on scanning laser ablation and inductively coupled plasma-mass spectrometry (SLA-ICPMS) and Raman micro-spectroscopy for the detection and identification of compounds consistent with gunshot residue particles (GSR) has been developed. The method has been applied to the characterization

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