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45963

Supelco

2,4-Dinitroaniline

analytical standard

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About This Item

Linear Formula:
(O2N)2C6H3NH2
CAS Number:
97-02-9
Molecular Weight:
183.12
Beilstein:
982999
EC Number:
202-553-5
MDL number:
MFCD00007151
UNSPSC Code:
41116107
PubChem Substance ID:
329757024

grade

analytical standard

Quality Level

100

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

176-178 °C (lit.)

application(s)

environmental

format

neat

SMILES string

Nc1ccc(cc1[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C6H5N3O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H,7H2

InChI key

LXQOQPGNCGEELI-UHFFFAOYSA-N

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General description

2,4-Dinitroaniline, typically derived as a nitro-substituted compound of aromatic amines, is an isomer of dinitroaniline, which finds primary use as an intermediate in the manufacture of dyestuff, pharmaceutical products, pesticides, etc.

Application

2,4-Dinitroaniline may be used as an analytical standard for the determination of the analyte in environmental water samples and wastewater samples by 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 Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 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)

435.2 °F - closed cup

Flash Point(C)

224 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ9084

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Xiaojia Huang et al.
Journal of chromatography. A, 1216(20), 4354-4360 (2009-04-03)
A simple and sensitive method for the determination of polar aromatic amines (PAAs) was developed using stir bar sorptive extraction (SBSE) coupling to high-performance liquid chromatography. A hydrophilic poly(vinylimidazole-divinylbenzene) (VIDB) monolithic material was prepared and acted as SBSE coating. The
José Raul Herance et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(22), 6491-6502 (2005-08-12)
Zeolites are suitable microporous hosts for positively charged organic species, but it is believed that they cannot adsorb organic anions. Pure Meisenheimer complex, derived from reduction of 2,4-dinitroaniline with NaBH4, was adsorbed inside faujasite cavities. Evidence for the internal incorporation
C Bolognesi et al.
Bollettino della Societa italiana di biologia sperimentale, 56(23), 2480-2485 (1980-12-15)
The DNA damage induced by in vivo administration of: 2,4-dinitroaniline, ortho-toluidine and para-toluidine, was determined using alkaline filter elution of DNA. The target organs for ultimate carcinogens produced in mice appear to be the liver and the kidney. The damage
P Gettins et al.
The Biochemical journal, 197(1), 119-125 (1981-07-01)
Pre-resonance Raman spectroscopy was used to study the interactions of the nitro groups of dinitrophenyl haptens with three dinitrophenyl-binding antibody fragments: M315 Fv, M460 Fab' and X25 Fab'. The observed changes in frequency of modes associated with the nitro moieties
S P Ozheredov et al.
TSitologiia i genetika, 43(5), 3-13 (2010-05-13)
The results of Allium-test screening of new 2,4- and 2,6-dinitroaniline derivates on antimitotic activity and phytotoxicity are presented in the work. It is revealed that all studied compounds which are derivates of 2,4-dinitroaniline, 2,6-dinitro-(4-fluoromethyl)-aniline as well as (methylsulfonyl) nitrobenzol, can
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