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ERD-152S

Supelco

2,4-Dinitrotoluene solution

10 mg/mL in acetonitrile, ampule of 5 mL, certified reference material, Cerilliant®

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About This Item

Fórmula empírica (Notação de Hill):
C7H6N2O4
Número CAS:
121-14-2
Peso molecular:
182.13
Número MDL:
MFCD00007172
Código UNSPSC:
41116107
NACRES:
NA.24

grau

certified reference material

Características

Snap-N-Spike®/Snap-N-Shoot®

embalagem

ampule of 5 mL

fabricante/nome comercial

Cerilliant®

concentração

10 mg/mL in acetonitrile

aplicação(ões)

environmental

formato

single component solution

temperatura de armazenamento

−20°C

InChI

1S/C7H6N2O4/c1-5-2-3-6(8(10)11)4-7(5)9(12)13/h2-4H,1H3

chave InChI

RMBFBMJGBANMMK-UHFFFAOYSA-N

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Informações legais

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

35.6 °F - closed cup

Ponto de fulgor (°C)

2 °C - closed cup

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Molly E Davidson et al.
ACS chemical biology, 8(1), 234-241 (2012-10-25)
Riboswitches are RNA sequences that regulate expression of associated downstream genes in response to the presence or absence of specific small molecules. A novel riboswitch that activates protein translation in E. coli cells in response to 2,4-dinitrotoluene (DNT) has been
Eric J Olson et al.
Journal of the American Chemical Society, 133(32), 12858-12865 (2011-07-09)
Polynitroaromatics are well-known to form anionic σ-complexes (Meisenheimer complexes). The formation of such complexes was assumed in the past to explain the blue color of solutions of 2,4-dinitrotoluene (DNT) and amines. However, this work shows that caution is warranted to
Tereza Hudcova et al.
Journal of hazardous materials, 192(2), 605-613 (2011-06-15)
The degradation efficiencies of isomeric mononitrotoluenes (2- and 4-NTs) and dinitrotoluenes (2,4-DNT and 2,6-DNT) by either individual bacterial strains (Bacillus cereus NDT4, Pseudomonas putida NDT1, Pseudomonas fluorescens NDT2, and Achromobacter sp. NDT3) or their mixture were compared in submerged batch
Maria Elisa Crestoni et al.
The Journal of chemical physics, 137(18), 181101-181101 (2012-11-21)
The bare deprotonated 2,4-dinitrotoluene [DNT-H](-) anion, formed by electrospray ionization and trapped in a Paul ion-trap, has been investigated by IR multiple photon dissociation (IRMPD) spectroscopy and quantum chemical calculations at the B3LYP∕6-311++G** level. IRMPD spectra were recorded in the
Yosuke Fukutani et al.
Biotechnology and bioengineering, 109(12), 3143-3151 (2012-06-26)
The goal of this work was to improve the bioluminescence-based signaling assay system to create a practical application of a biomimetic odor sensor using an engineered yeast-expressing olfactory receptors (ORs). Using the yeast endogenous pheromone receptor (Ste2p) as a model
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