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Merck
CN

42155

2,3-Dinitrophenol

moistened with water, ≥98.0% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C6H4N2O5
CAS Number:
66-56-8
Molecular Weight:
184.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57650101
EC Number:
200-628-7
Beilstein/REAXYS Number:
2213580
MDL number:
MFCD00024250
Assay:
≥98.0% (HPLC)

Key Documents

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InChI

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

InChI key

MHKBMNACOMRIAW-UHFFFAOYSA-N

SMILES string

Oc1cccc(c1[N+]([O-])=O)[N+]([O-])=O

assay

≥98.0% (HPLC)

quality

moistened with water

contains

~20% water as stabilizer

mp

141-145 °C

General description

2,3-Dinitrophenol is a nitroaromatic compound. It has been reported to exhibit high acute toxicity to Scenedesmus obliquus, with EC50 value of 2.5±0.8.

Application

2,3-Dinitrophenol may be employed as nitrogen supplement for the bacterial culture medium.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Expl. 1.1 - STOT RE 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
047055/1
1380530
1354265
042100/1
040679/1

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C Bruhn et al.
Applied and environmental microbiology, 53(1), 208-210 (1987-01-01)
Bacteria which utilized nitroaromatic compounds (0.5 mM) as sole source of nitrogen were isolated from soil. With 2,6-dinitrophenol and succinate as carbon source, a Pseudomonas strain was isolated which liberated and assimilated nitrite. Approximately 2 mol of NO(2) per mol
María Almuedo-Castillo et al.
Nature cell biology, 20(9), 1032-1042 (2018-08-01)
Individuals can vary substantially in size, but the proportions of their body plans are often maintained. We generated smaller zebrafish by removing 30% of their cells at the blastula stages and found that these embryos developed into normally patterned individuals.
Xiangqin Jin et al.
Computers in biology and medicine, 51, 205-213 (2014-06-25)
Although numerous chemicals have been identified to have significant toxicological effect on aquatic organisms, there is still lack of a reliable, high-throughput approach to evaluate, screen and monitor the presence of organic contaminants in aquatic system. In the current study
A Motzik et al.
Oncogene, 36(33), 4732-4738 (2017-04-11)
Microphthalmia transcription factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein. This transcription factor plays a crucial role in the physiological and pathological functions of distinct cell types. MITF transcriptional activity is inhibited by the histidine triad nucleotide-binding
Eric Y Umemoto et al.
Toxicology letters, 229(1), 198-209 (2014-06-10)
Carbon nanotubes (CNT) are environmental challenges to the respiratory and gastrointestinal mucosa, and to the dermal immune system. Mast cells (MC) are pro-inflammatory immunocytes that reside at these interfaces with the environment. Mast cells are sources of pro-inflammatory mediators (histamine
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