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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

Empirical Formula (Hill Notation):
C7H7N3O4
CAS Number:
19406-51-0
Molecular Weight:
197.15
MDL number:
MFCD00033978
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

packaging

vial of 100 mg

manufacturer/tradename

Cerilliant®

application(s)

environmental

format

neat

storage temp.

room temp

SMILES string

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

InChI key

KQRJATLINVYHEZ-UHFFFAOYSA-N

General description

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.

Legal Information

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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Mehilal et al.
Journal of hazardous materials, 84(2-3), 117-122 (2001-06-19)
A chemoselective reductive method has been achieved for the preparation of 4-picrylamino-2,6-dinitrotoluene (PADNT), a new insensitive energetic material which has been characterised by spectral data and elemental analysis. Some explosive properties of the compound have also been determined and the
B H Woollen et al.
British journal of industrial medicine, 43(7), 465-473 (1986-07-01)
Trinitrotoluene (TNT) absorption was assessed in groups of workers at two explosives factories by measuring the urinary concentrations of dinitroaminotoluene (DNAT) metabolites. DNAT was detected in most of the urine samples analysed and for postshift samples the mean (SD) concentration
G Ahlborg et al.
British journal of industrial medicine, 45(5), 353-358 (1988-05-01)
Urine samples taken after work and after a free weekend from 50 workers employed in various activities in a chemical plant manufacturing explosives were analysed. On the basis of hygienic surveys, the subjects were divided into three categories of exposure
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
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
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