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Merck
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Documentos clave

47749-U

Supelco

2-Amino-4,6-dinitrotoluene solution

certified reference material, 1000 μg/mL in acetonitrile

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About This Item

Fórmula empírica (notación de Hill):
C7H7N3O4
Número de CAS:
35572-78-2
Peso molecular:
197.15
Código UNSPSC:
77101502
NACRES:
NA.24

grado

certified reference material
TraceCERT®

Agency

EPA 8330

Características

standard type calibration

concentración

1000 μg/mL in acetonitrile

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

environmental

Formato

single component solution

temp. de almacenamiento

2-8°C

InChI

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

Clave InChI

IEEJAAUSLQCGJH-UHFFFAOYSA-N

Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Otras notas

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Información legal

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

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

35.6 °F - closed cup

Punto de inflamabilidad (°C)

2.0 °C - closed cup

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Certificados de análisis (COA)

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G S Nyanhongo et al.
Journal of hazardous materials, 165(1-3), 285-290 (2008-11-18)
Pseudomonas putida GG04 and Bacillus SF have been successfully incorporated into an explosive formulation to enhance biotransformation of TNT residues and/or explosives which fail to detonate due to technical faults. The incorporation of the microorganisms into the explosive did not
Petra M Krämer et al.
Analytical and bioanalytical chemistry, 382(8), 1919-1933 (2005-07-28)
Five new rat monoclonal antibodies (mAbs) for 2,4,6-trinitrotoluene (TNT) and other nitroaromatic compounds, including, especially, the metabolite 2-amino-4,6-dinitrotoluene (2-ADNT), are described. Five heterogeneous, competitive enzyme-linked immunosorbent assays (ELISAs) were developed. Assay 1 uses mAb DNT4 3F6 as recognition element and
Hirendranath Banerjee et al.
Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 28(3), 231-234 (2009-11-06)
During microbial or mammalian cell metabolism, TNT (2,4,6-tinitrotoluene) is reduced to 2Am-DNT (2-amino-4,6-dinitrotoluene), 4Am-DNT, or 2,4-diamino-NT (2,4-diaminonitrotoluelne) depending on the specific organism. The metabolite 2Am-DNT is the most common of the TBT biotransformation pathways in bacterial and fungal species studied
Jason T Popesku et al.
Applied microbiology and biotechnology, 65(6), 739-746 (2004-05-11)
Metabolites formed during 2,4,6-trinitrotoluene (TNT) removal by a mixed bacterial culture (acclimated and maintained on crude oil-containing medium and capable of high rates of TNT removal) were characterized. In resting cell experiments in the absence of glucose, 46.2 mg/l TNT
Alethea T Bowen et al.
Chemosphere, 63(1), 58-63 (2005-12-06)
Tubifex tubifex metabolizes 2,4,6-trinitrotoluene (TNT) to 2-amino-4,6-dinitrotoluene (2ADNT) and 4-amino-2,6-dinitrotoluene (4ADNT). Elimination rates of metabolically-generated ADNTs are low compared to ADNTs absorbed directly from water, suggesting that metabolically-generated ADNTs may be bound or sequestered within tissue and therefore less available
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