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185329

Sigma-Aldrich

3-Nitrobenzoic acid

ReagentPlus®, 99%

Sinónimos:

m-Carboxynitrobenzene, m-Nitrobenzenecarboxylic acid, m-Nitrobenzoic acid

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About This Item

Fórmula lineal:
O2NC6H4CO2H
Número de CAS:
121-92-6
Peso molecular:
167.12
Beilstein/REAXYS Number:
908644
EC Number:
204-508-5
MDL number:
MFCD00007251
UNSPSC Code:
12352100
eCl@ss:
39032047
PubChem Substance ID:
24850684
NACRES:
NA.22

Quality Level

200

product line

ReagentPlus®

assay

99%

form

solid

mp

139-141 °C (lit.)

solubility

water: soluble 3 g/L at 25 °C

functional group

carboxylic acid
nitro

SMILES string

OC(=O)c1cccc(c1)[N+]([O-])=O

InChI

1S/C7H5NO4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H,(H,9,10)

InChI key

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

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General description

3-Nitrobenzoic acid forms molecular adducts with commercially important herbicides and pesticides such as amitrole.

Application

3-Nitrobenzoic acid was used to investgate the role of ozone as additional decomposition or finishing reagent in the degradation of o-, m- and p-nitobenzoic acids.

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

373.3 °F - Pensky-Martens closed cup

flash_point_c

189.6 °C - Pensky-Martens closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCM5557
BCCK4580
BCCJ8019
BCCH1833
BCCJ0780

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Molecular co-crystals of carboxylic acids. 16. 1: 1 Adduct of 3-nitrobenzoic acid with 3-amino-1H-1, 2, 4-triazole.
Lynch DE, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 50(8), 1291-1294 (1994)
W Jiang et al.
The Analyst, 122(3), 211-215 (1997-03-01)
In an attempt to produce complete oxidation of a biological matrix, bovine liver, ozone was investigated as an additional, potentially non-contaminating, oxidizing reagent after nitric acid digestion. Experiments were carried out to determine the decomposition efficiency of residual carbon species
Zhiqiang Hu et al.
Water research, 39(15), 3501-3510 (2005-07-30)
Biodegradation rates of benzoate and related aromatic compounds, 3-nitrobenzoate, 4-chlorobenzoate, 4-chlorophenol, and 2,4-dichlorophenol by unexposed (unacclimated) and long-term exposed (acclimated) biomass were quantified using a modified fed-batch technique. The acclimated biomass was taken after approximately 1-year of operation from three
M Algarra et al.
Talanta, 83(5), 1335-1340 (2011-01-18)
The detection of nitroaromatic compounds, best known as raw materials in explosives preparations, is important in many fields including environmental science, public security and forensics. CdSe quantum dots capped with PAMAM-G(4) dendrimer were synthetized in water and used for the
B D'eng et al.
Voprosy meditsinskoi khimii, 29(6), 113-117 (1983-11-01)
Hepatotoxic effects of 4-chloro-3-nitrobenzoic acid (x-NBA), 3-nitrobenzoic acid (NBA) and 4-chlorobenzoic acid (CBA) were studied at the doses corresponding to LD50, 1/10 LD50 and 1/50 LD50. The toxic effects were estimated by monitoring alterations in activity of protein-synthesizing system in
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