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442597

Supelco

Formaldehyde-2,4-DNPH

analytical standard

Synonym(s):

Formaldehyde-2,4-dinitrophenylhydrazone

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About This Item

Linear Formula:
H2C=NNHC6H3(NO2)2
CAS Number:
1081-15-8
Molecular Weight:
210.15
Beilstein/REAXYS Number:
750330
MDL number:
MFCD00191364
UNSPSC Code:
12000000
PubChem Substance ID:
24867923

grade

analytical standard

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 100 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

153-156 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

SMILES string

[O-][N+](=O)c1ccc(NN=C)c(c1)[N+]([O-])=O

InChI

1S/C7H6N4O4/c1-8-9-6-3-2-5(10(12)13)4-7(6)11(14)15/h2-4,9H,1H2

InChI key

UEQLSLWCHGLSML-UHFFFAOYSA-N

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General description

Formaldehyde 2,4-dinitro­phenyl­hydrazone (C7H6N4O4) is a planar molecule and the nitro groups are almost coplanar with the benzene ring.

Application

Formaldehyde-2,4-DNPH may be used as an analytical standard for the determination of the analyte in air samples, food and feed products, and aquatic products by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
LRAC7357
LRAC0075
LRAB8437
LRAB6069
LC23432V

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Formaldehyde 2, 4-dinitrophenylhydrazone.
Tameem AA
Acta Crystallographica Section E, Structure Reports Online, 63 (1), 57-58 (2006)
Trace determination of carbonyl compounds in air by gas chromatography of their 2, 4-dinitrophenylhydrazones
Smith RA and Drummond I
Analyst, 104(1242), 875-877 (1979)
Shigehisa Uchiyama et al.
Journal of chromatography. A, 996(1-2), 95-102 (2003-07-02)
The most widely used method for qualitative and quantitative analysis of carbonyl compounds is the 2,4-dinitrophenylhydrazine method through the formation of 2,4-dinitrophenylhydrazone derivatives. However, this method may cause an analytical error because 2,4-dinitrophenylhydrazones have both E- and Z-stereoisomers. Purified aldehyde-2,4-dinitrophenylhydrazone
Shiuh-Dih Chou et al.
Molecular immunology, 45(4), 971-980 (2007-09-14)
We have previously reported that Major Histocompatibility Complex (MHC) class II can be induced by histone deacetylase inhibitors (HDACi) in the absence of class II transactivator (CIITA). Here we characterized the histone modifications associated with the CIITA-dependent (IFN-gamma induced) and
Teresa M Lamb et al.
PloS one, 6(11), e27149-e27149 (2011-11-17)
MAPK signal transduction pathways are important regulators of stress responses, cellular growth, and differentiation. In Neurospora, the circadian clock controls rhythms in phosphorylation of the p38-like MAPK (OS-2); however, the mechanism for this regulation is not known. We show that
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