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Supelco

2,3-Dinitrotoluene

analytical standard

Synonym(s):

2,3-DNT, 2,4-DNT

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About This Item

Linear Formula:
CH3C6H3(NO2)2
CAS Number:
Molecular Weight:
182.13
Beilstein:
2212428
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

59-61 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Cc1cccc(c1[N+]([O-])=O)[N+]([O-])=O

InChI

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

InChI key

DYSXLQBUUOPLBB-UHFFFAOYSA-N

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General description

2,3-Dinitrotoluene is classified under the group of nitroaromatic compounds, which are organic nitro derivatives of analytical research interest. It is considered as a ubiquitous environmental contaminant and can adversely affect human health because of its mutagenic and/or carcinogenic nature.

Application

2,3-Dinitrotoluene may be used as an analytical standard for the determination of the analyte in forensic samples, explosive-contaminated groundwater samples, industrial effluents and seawater samples by various chromatographic techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

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Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Muta. 2 - Repr. 2 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Coupled solid phase extraction-supercritical fluid extraction-on-line gas chromatography of explosives from water
Slack GC, et al.
Journal of High Resolution Chromatography, 16(8), 473-478 (1993)
E Psillakis et al.
Journal of chromatography. A, 907(1-2), 211-219 (2001-02-24)
The application of solvent microextraction to the analysis of nitroaromatic explosives is presented. Extraction of 11 nitroaromatics was achieved by suspending 1 microl of organic solvent to the tip of a microsyringe in a stirred aqueous solution. Parameters such as
Neera Singh et al.
Journal of hazardous materials, 173(1-3), 343-348 (2009-09-15)
The sorption of organic contaminants in soil is mainly attributed to the soil organic matter (SOM) content. However, recent studies have highlighted the fact that it is not the total carbon content of the organic matter, but its chemical structure
Application of high-field proton nuclear magnetic resonance (1 H-NMR) spectroscopy for the analysis of explosives and related compounds in groundwater samples-a comparison with the high-performance liquid chromatography (HPLC) method
Preiss A, et al.
Fresenius Journal of Analytical Chemistry, 356(7), 445-451 (1996)
Igor A Buryakov
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 800(1-2), 75-82 (2003-12-31)
Description of a gas chromatograph designed for express analysis of explosives (2,4-dinitrotoluene, 2,4,6-trinitrotoluene, pentaerythritol tetranitrate), chemical warfare agents (mustard gas, lewisite, sarin) and drugs (heroin, cocaine hydrochloride, crack) is given. The devices comprises a multicapillary chromatographic column and an ion

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