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Merck
CN

41910

2,4-二硝基苯甲酸

technical, ≥95.0% (HPLC)

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线性分子式:
(O2N)2C6H3CO2H
化学文摘社编号:
分子量:
212.12
EC Number:
210-219-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
658650
MDL number:
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grade

technical

assay

≥95.0% (HPLC)

mp

176-180 °C (lit.), 176-184 °C

solubility

dioxane: 50 mg/mL, clear

SMILES string

OC(=O)c1ccc(cc1[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C7H4N2O6/c10-7(11)5-2-1-4(8(12)13)3-6(5)9(14)15/h1-3H,(H,10,11)

InChI key

ZIIGSRYPZWDGBT-UHFFFAOYSA-N

法规信息

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D Gisi et al.
Applied microbiology and biotechnology, 48(4), 441-448 (1997-12-09)
A mixed culture of microorganisms able to utilize 4,6-dinitro-ortho-cresol (DNOC) as the sole source of carbon, nitrogen and energy was isolated from soil contaminated with pesticides and from activated sludge. DNOC was decomposed aerobically in batch cultures as well as
Yong-Hak Kim et al.
Journal of bacteriology, 195(2), 180-192 (2012-11-06)
2-Nitrobenzoate 2-nitroreductase (NbaA) of Pseudomonas fluorescens strain KU-7 is a unique enzyme, transforming 2-nitrobenzoic acid (2-NBA) and 2,4-dinitrobenzoic acid (2,4-DNBA) to the 2-hydroxylamine compounds. Sequence comparison reveals that NbaA contains a conserved cysteine residue at position 141 and two variable
Hugo Guillén et al.
Journal of agricultural and food chemistry, 57(21), 10457-10465 (2009-10-16)
Nitroreductases reduce nitroaromatic compounds and other oxidants in living organisms, having interesting implications in environmental and human health. A putative nitrobenzoate reductase encoding gene (lp_0050) was recently annotated in the completed DNA sequence of lactic acid bacterium Lactobacillus plantarum WCFS1
J Angerer et al.
Journal of chromatography. B, Biomedical sciences and applications, 713(2), 313-322 (1998-09-24)
The method of analysis described permits the determination of 2,4-dinitrobenzoic acid down to the lower microg l(-1) range in the urine of persons exposed to dinitrotoluene. 2,4-Dinitrobenzoic acid is the main metabolite of 2,4-dinitrotoluene and technical dinitrotoluene. After acidic hydrolysis

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