产品名称
2,4-二硝基苯胺, analytical standard
InChI key
LXQOQPGNCGEELI-UHFFFAOYSA-N
InChI
1S/C6H5N3O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H,7H2
SMILES string
Nc1ccc(cc1[N+]([O-])=O)[N+]([O-])=O
grade
analytical standard
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
Quality Level
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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.
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.
Other Notes
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.
signalword
Danger
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2
存储类别
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
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
非剧毒-急性毒性1
危险化学品
此项目有
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
[Experimental study of the effect of 2,4-dinitroaniline on embryogenesis].
S E Khipko et al.
Gigiena truda i professional'nye zabolevaniia, (6)(6), 47-49 (1982-06-01)
H B Matthews et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(1), 1-10 (1986-01-01)
The disposition and metabolism of 2,4-dinitroaniline was studied in male F-344 rats following oral and i.v. administration. Gastrointestinal absorption was near complete and was not affected by dose (10-90 mumol/kg). Following either oral or i.v. administration, dinitroaniline was rapidly distributed
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