Skip to Content
Merck
All Photos(1)

Documents

ERD-152S

Supelco

2,4-Dinitrotoluene solution

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

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C7H6N2O4
CAS Number:
Molecular Weight:
182.13
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 5 mL

manufacturer/tradename

Cerilliant®

concentration

10 mg/mL in acetonitrile

application(s)

environmental

format

single component solution

storage temp.

−20°C

InChI

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

InChI key

RMBFBMJGBANMMK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Legal Information

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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service