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2,4-dinitrophenylhydrazine

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EntityQ209227· pop 23· linked from 61 articles

2,4-dinitrophenylhydrazine

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Also known as Brady's reagent, 2,4-DNP hydrazine, 1-Hydrazino-2,4-dinitrobenzene, 2,4-Dnph

2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C6H3(NO2)2NHNH2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.

In the Vinony graph

Within Vinony's link graph, 2,4-dinitrophenylhydrazine is referenced by 61 other articles, and connects out to hydrazide, International Standard Book Number and analytical chemistry.

It sits within the topics Chembox having GHS data, Chembox image size set and ECHA InfoCard ID from Wikidata.

Its subject is documented across 22 Wikipedia language editions.

Chemical data

Formula
C6H6N4O4
Molecular weight
198.14 g/mol
IUPAC name
(2,4-dinitrophenyl)hydrazine
SMILES
C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NN
InChIKey
HORQAOAYAYGIBM-UHFFFAOYSA-N
XLogP
1.5
Polar surface area
130 Ų
H-bond donors
2
H-bond acceptors
6
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
carbon
Mass
198.038905
Show 4 more facts
chemical formula
C₆H₆N₄O₄
canonical SMILES
C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NN
Commons category
2,4-Dinitrophenylhydrazine
melting point
201
Sources (3)

via Wikidata · CC0

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Encyclopedic overview

5 sections
Contents
  • Synthesis
  • DNP test
  • Safety
  • See also
  • References

2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C6H3(NO2)2NHNH2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.

==Synthesis== It can be prepared by the reaction of hydrazine sulfate with 2,4-dinitrochlorobenzene: 300px

Excerpted from Wikipedia’s “2,4-dinitrophenylhydrazine” article, available under the CC BY-SA 4.0 licence.

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