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Supelco

2,4-Dinitrophenol

PESTANAL®, analytical standard

Synonym(s):

α-Dinitrophenol, 2,4-DNP, DNP

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About This Item

Linear Formula:
(O2N)2C6H3OH
CAS Number:
51-28-5
Molecular Weight:
184.11
Beilstein:
1246142
EC Number:
200-087-7
MDL number:
MFCD00007115
UNSPSC Code:
41116107
PubChem Substance ID:
329754950
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

6.35 (vs air)

product line

PESTANAL®

quality

(with approx. 0,3 ml H2O/g)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

108-112 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Oc1ccc(cc1[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C6H4N2O5/c9-6-2-1-4(7(10)11)3-5(6)8(12)13/h1-3,9H

InChI key

UFBJCMHMOXMLKC-UHFFFAOYSA-N

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General description

2,4-Dinitrophenol is called as an uncoupler of oxidative phosphorylation, which can prevent adenosine triphosphate(ATP) synthesis, but it permits electron transfer to proceed.
2,4-Dinitrophenol is called as an uncoupler of oxidative phosphorylation, which can prevent adenosine triphosphate(ATP) synthesis, but it permits electron transfer to proceed.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Desen. Expl. 4 - STOT RE 1

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF1229
BCCD2521
BCBT2071
SZBG053XV
SZBF118XV

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2-Nitrophenol 98%

Sigma-Aldrich

N19702

2-Nitrophenol

Biochemistry Biochemistry: Solutions Manual (1998)
Biochemistry Biochemistry: Solutions Manual (1998)
Stephanie C Weber et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(19), 7338-7343 (2012-04-21)
Chromosomal loci jiggle in place between segregation events in prokaryotic cells and during interphase in eukaryotic nuclei. This motion seems random and is often attributed to brownian motion. However, we show here that locus dynamics in live bacteria and yeast
Tatsuya Oka et al.
The Journal of allergy and clinical immunology, 132(4), 922-932 (2013-07-03)
Rapid desensitization transiently prevents severe allergic reactions, allowing administration of life-saving therapies in previously sensitized patients. However, the mechanisms underlying successful rapid desensitization are not fully understood. We sought to investigate whether the mast cell (MC) is an important target
Manisha V Bagal et al.
Ultrasonics sonochemistry, 20(5), 1226-1235 (2013-03-30)
In the present work, degradation of 2,4-dinitrophenol (DNP), a persistent organic contaminant with high toxicity and very low biodegradability has been investigated using combination of hydrodynamic cavitation (HC) and chemical/advanced oxidation. The cavitating conditions have been generated using orifice plate
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Separation of 2-Chlorophenol; 2,4-Dichlorophenol; 2,4,6-Tribromophenol; 2,4,6-Trichlorophenol; 2,4-Dinitrophenol; Pentafluorophenol; 2-Methylphenol, analytical standard; 2,3,4,6-Tetrachlorophenol; Pentachlorophenol; 4-Nitrophenol; 2-Bromophenol; 2,3,5,6-Tetrachlorophenol; 2,3,5-Trichlorophenol; 4-Chloro-3-methylphenol; 2,4,5-Trichlorophenol; 4-Methylphenol, analytical standard; 2,4-Dimethylphenol; 2-Nitrophenol; 3-Methylphenol, analytical standard; Phenol; 2-Methyl-4,6-dinitrophenol; 2,3,4-Trichlorophenol; 2,6-Dichlorophenol; 2,3,4,5-Tetrachlorophenol

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