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ERA-018

Supelco

4-Amino-2,6-dinitrotoluene

vial of 100 mg, analytical standard, Cerilliant®

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About This Item

Formule empirique (notation de Hill) :
C7H7N3O4
Numéro CAS:
19406-51-0
Poids moléculaire :
197.15
Numéro MDL:
MFCD00033978
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Conditionnement

vial of 100 mg

Fabricant/nom de marque

Cerilliant®

Application(s)

environmental

Format

neat

Température de stockage

room temp

Chaîne SMILES 

NC1=CC([N+]([O-])=O)=C(C)C([N+]([O-])=O)=C1

InChI

1S/C7H7N3O4/c1-4-6(9(11)12)2-5(8)3-7(4)10(13)14/h2-3H,8H2,1H3

Clé InChI

KQRJATLINVYHEZ-UHFFFAOYSA-N

Description générale

4-Amino-2,6-dinitrotoluene (4A2,6-ADNT) is a metabolite of 2,4,6-trinitrotoluene, which is widely used as an explosive in military shells, bombs, and grenades.

Application

4-Amino-2,6-dinitrotoluene may be used as an analytical standard for the determination of the analyte in explosives residues, ammunition waste, and urine by chromatography techniques.

Informations légales

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Skull and crossbonesHealth hazardEnvironment
GHS06,GHS08,GHS09

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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J Yinon et al.
Toxicology letters, 26(2-3), 205-209 (1985-08-01)
Metabolites of 2,4,6-trinitrotoluene (TNT) were found in the urine of rats fed with TNT. The urine extracts were analysed by liquid chromatography-mass spectrometry (LC-MS). Metabolites found included TNT itself as well as 2-amino-4,6-dinitrotoluene, 4-amino-2,6-dinitrotoluene and 2,4-diamino-6-nitrotoluene, indicating that reduction processes
C-J Wang et al.
Archives of environmental contamination and toxicology, 42(1), 1-8 (2001-11-14)
Oxidative coupling of nitroaromatic compounds involving soil organic matter was examined as a means of soil remediation. Humic monomers, serving as model compounds for soil humic substances, were used as cosubstrates, applying phenoloxidases (laccase from Trametes villosa and peroxidase from
J Yinon et al.
Biomedical mass spectrometry, 11(11), 594-600 (1984-11-01)
A series of metabolites of trinitrotoluene (TNT) have been synthesized and analysed by electron impact (EI) and chemical ionization (CI) mass spectrometry. Identification characteristics of these metabolites by their mass spectra have been determined. Differentiation of isomers is made possible
L R Johnson et al.
Ecotoxicology and environmental safety, 27(1), 23-33 (1994-02-01)
Coexposure of 2,4,6-trinitrotoluene (TNT), 2-amino-4,6-dinitrotoluene (2A), or 4-amino-2,6-dinitrotoluene (4A) to near-ultraviolet (nuv) light (lambda max-354 nm) significantly enhanced their toxicity toward Photobacterium phosphoreum (Microtox bioassay) during 30 min but not 15 min. Based on the slopes of the dose-response lines
Viktor Vorísek et al.
Journal of analytical toxicology, 29(1), 62-65 (2005-04-06)
A routine procedure for the monitoring of occupational exposure to 2,4,6-trinitrotoluene (TNT) based on the semiquantitative determination of 4-amino-2,6-dinitrotoluene (4A2,6-DNT) in urine samples by gas chromatography (GC-MS) was developed. For calibration purposes, a standard sample of 4-amino-4,6-dinitrotoluene was prepared. Urine
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