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Merck
CN

47749-U

2-氨基-4,6-二硝基甲苯 溶液

certified reference material, 1000 μg/mL in acetonitrile

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关于此项目

经验公式(希尔记法):
C7H7N3O4
化学文摘社编号:
分子量:
197.15
UNSPSC Code:
77101502
NACRES:
NA.24
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产品名称

2-氨基-4,6-二硝基甲苯 溶液, certified reference material, 1000 μg/mL in acetonitrile

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

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

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

signalword

Danger

Hazard Classifications

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

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup

法规信息

危险化学品
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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
Craig A McFarland et al.
Environmental pollution (Barking, Essex : 1987), 159(2), 466-473 (2010-11-12)
The compound 2-amino-4,6-dinitrotoluene (2A-DNT) was evaluated under laboratory conditions in the Western fence lizard (Sceloporus occidentalis) to assess the potential for reptile toxicity. Oral LD(50) values were 1406 and 1867 mg/kg for male and female lizards, respectively. Based on responses
Michael J Quinn et al.
Ecotoxicology (London, England), 19(5), 945-952 (2010-03-10)
2-Amino-4,6-dinitrotoluene (2A-DNT) is a metabolite of the explosive 2,4,6-trinitrotoluene (TNT) which is present in the soil at numerous U.S. Army installations as the result of TNT manufacture or training activities. Although many avian species are known to inhabit areas where
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

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