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Merck

45963

Supelco

2,4-二硝基苯胺

analytical standard

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About This Item

线性分子式:
(O2N)2C6H3NH2
CAS号:
分子量:
183.12
Beilstein:
982999
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:

等级

analytical standard

质量水平

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

176-178 °C (lit.)

应用

environmental

包装形式

neat

SMILES字符串

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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一般描述

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.

应用

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.

推荐产品

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

警示用语:

Danger

危险分类

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2

储存分类代码

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

WGK

WGK 3

闪点(°F)

435.2 °F - closed cup

闪点(°C)

224 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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