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Merck
CN

47749-U

Supelco

2-Amino-4,6-dinitrotoluene solution

certified reference material, 1000 μg/mL in acetonitrile

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About This Item

Empirical Formula (Hill Notation):
C7H7N3O4
CAS Number:
35572-78-2
Molecular Weight:
197.15
UNSPSC Code:
77101502
NACRES:
NA.24

Key Documents

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grade

certified reference material
TraceCERT®

Agency

EPA 8330

feature

standard type calibration

concentration

1000 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

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

InChI key

IEEJAAUSLQCGJH-UHFFFAOYSA-N

Application

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

Other Notes

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.

Legal Information

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2.0 °C - closed cup

Regulatory Information

危险化学品

Certificates of Analysis (COA)

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L R Krumholz et al.
Journal of industrial microbiology & biotechnology, 18(2-3), 161-169 (1997-02-01)
The transport and fate of pollutants is often governed by both their tendency to sorb as well as their susceptibility to biodegradation. We have evaluated these parameters for 2,4,6-trinitrotoluene (TNT) and several biodegradation products. Slurries of aquifer sediment and groundwater
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
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
K Scheibner et al.
Journal of basic microbiology, 38(1), 51-59 (1998-05-09)
Preparations of extracellular manganese peroxidase from the white-rot fungus Nematoloma frowardii and the litter decaying fungus Stropharia rugosoannulata converted rapidly the main intermediates of the explosive 2,4,-trinitrotoluene--the aminonitrotoluenes. In a cell-free system, 2-amino-4,6-dinitrotoluene, 4-amino-2,6-dinitrotoluene and 2,6-diamino-4-nitrotoluene were degraded without formation
Neera Singh et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 43(4), 348-356 (2008-02-15)
Trinitrotoluene (TNT), a nitroaromatics, is a major pollutant in explosive contaminated soils. Present study reports the effect of initial concentration of TNT on its degradation kinetics in soils. Soils from two contaminated sites viz. Clausthal and Elsnig, Germany, were mixed
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