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Merck

ERA-018

Supelco

4-Amino-2,6-dinitrotoluene

vial of 100 mg, analytical standard, Cerilliant®

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About This Item

Fórmula empírica (notación de Hill):
C7H7N3O4
Número de CAS:
Peso molecular:
197.15
Número MDL:
Código UNSPSC:
41116107
NACRES:
NA.24

grado

analytical standard

envase

vial of 100 mg

fabricante / nombre comercial

Cerilliant®

aplicaciones

environmental

Formato

neat

temp. de almacenamiento

room temp

cadena 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

Clave InChI

KQRJATLINVYHEZ-UHFFFAOYSA-N

Descripción general

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.

Aplicación

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.

Información legal

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

Palabra de señalización

Danger

Clasificaciones de peligro

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

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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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
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
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

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