45965
1,2-Dinitrobenzene
analytical standard
Synonym(s):
1,2-DNB
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All Photos(2)
About This Item
Linear Formula:
C6H4(NO2)2
CAS Number:
Molecular Weight:
168.11
Beilstein:
642224
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
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grade
analytical standard
Quality Level
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
bp
319 °C/773 mmHg (lit.)
mp
114-117 °C (lit.)
application(s)
environmental
format
neat
SMILES string
[O-][N+](=O)c1ccccc1[N+]([O-])=O
InChI
1S/C6H4N2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H
InChI key
IZUKQUVSCNEFMJ-UHFFFAOYSA-N
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General description
1,2-Dinitrobenzene belongs to the class of nitroaromatic compounds, which are utilized for the manufacture of pesticides, explosives, polymers, etc. They can pose a potential risk to the environment because of their toxic nature.
Application
1,2-Dinitrobenzene has been used as an analytical standard for the determination of the analyte in organic explosives investigated during the forensic analysis by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS). It may be used as an analytical standard for the determination of the analyte in aqueous samples, environmental samples and human biological 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.
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - 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)
302.0 °F - closed cup
Flash Point(C)
150 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Application of DLLME based on the solidification of floating organic droplets for the determination of dinitrobenzenes in aqueous samples
Wu Y, et al.
Chromatographia, 72(7-8), 695-699 (2010)
M E Walsh
Talanta, 54(3), 427-438 (2008-10-31)
Hazardous waste site characterization, forensic investigations, and land mine detection are scenarios where soils may be collected and analyzed for traces of nitroaromatic, nitramine, and nitrate ester explosives. These thermally labile analytes are traditionally determined by high-performance liquid chromatography (HPLC);
S Jönsson et al.
Journal of chromatography. A, 1164(1-2), 65-73 (2007-08-04)
A solid-phase microextraction (SPME) method using gas chromatography-electron-capture negative ionisation mass spectrometry (GC-ECNI-MS) and isotope dilution quantification for the analysis of nitroaromatic compounds in complex, water based samples has been optimised. For ionisation, ECNI was the most sensitive and selective
J V Barbo et al.
Journal of immunology (Baltimore, Md. : 1950), 154(4), 1551-1559 (1995-02-15)
A population of CD8+ T cells from dinitrobenzene sulfonate-primed mice produce soluble effector molecules that down-regulate the magnitude of dinitrophenol-specific contact hypersensitivity reactions. These soluble molecules express the binding specificity and serologic determinants of alpha/beta TCR. To examine the requirement
H Tamaki et al.
Journal of bacteriology, 181(9), 2958-2962 (1999-04-28)
Glutathione S-transferases (GSTs) Y-1 and Y-2 from the yeast Issatchenkia orientalis were purified by passage through a glutathione-agarose column, and the cDNA for GST Y-1 was cloned and sequenced. The deduced amino acid sequence consisted of 188 residues with a
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