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Safety Information

185329

Sigma-Aldrich

3-Nitrobenzoic acid

ReagentPlus®, 99%

Synonym(s):

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

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About This Item

Linear Formula:
O2NC6H4CO2H
CAS Number:
121-92-6
Molecular Weight:
167.12
Beilstein:
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

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

373.3 °F - Pensky-Martens closed cup

Flash Point(C)

189.6 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

185329-5G:
185329-BULK:
185329-VAR:
185329-100G:
185329-500G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5557
BCCK4580
BCCJ8019
BCCH1833
BCCJ0780

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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
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)
Miguel A Providenti et al.
Applied and environmental microbiology, 72(4), 2651-2660 (2006-04-07)
In Comamonas sp. strain JS46, 3-nitrobenzoate (3Nba) is initially oxidized at the 3,4 position by a dioxygenase, which results in release of nitrite and production of protocatechuate. The locus coding for the 3Nba dioxygenase (designated mnb, for m-nitrobenzoate) was mobilized
Zhiqiang Hu et al.
Water research, 39(4), 710-720 (2005-02-15)
The physical and biochemical characteristics of the biomass in three lab-scale sequencing batch reactors (SBR) treating a synthetic wastewater at a 20-day target solids retention time (SRT) were investigated. The synthetic wastewater feed contained biogenic compounds and 22 organic priming
Reproductive toxicology. m-Nitrobenzoic acid.
Environmental health perspectives, 105 Suppl 1, 325-326 (1997-02-01)
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