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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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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.

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

Regulatory Information

非剧毒-急性毒性1
危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ9084

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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
[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)
T Azuma et al.
Biochemistry, 27(16), 6116-6120 (1988-08-09)
The interaction of M315 with 2,4-dinitrophenyl haptens was studied. 2,4-Dinitroaniline (DNP-NH2) showed maximum affinity to M315 at about pH 4. The pH dependence of the association constant of DNP-NH2 to M315 showed three transitions at pH 4.7, at pH 7.2
O Zelenko et al.
Nucleic acids research, 22(14), 2731-2739 (1994-07-25)
The synthesis and enzymatic characterization of DUPAAA, a novel fluorogenic substrate for RNases of the pancreatic type is described. It consists of the dinucleotide uridylyl-3',5'-deoxyadenosine to which a fluorophore, o-aminobenzoic acid, and a quencher, 2,4-dinitroaniline, have been attached by means
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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