Skip to Content
Merck
CN

185329

3-Nitrobenzoic acid

ReagentPlus®, 99%

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
O2NC6H4CO2H
CAS Number:
121-92-6
Molecular Weight:
167.12
NACRES:
NA.22
PubChem Substance ID:
24850684
eCl@ss:
39032047
UNSPSC Code:
12352100
EC Number:
204-508-5
MDL number:
MFCD00007251
Beilstein/REAXYS Number:
908644

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Nitrobenzoic acid, ReagentPlus®, 99%

InChI key

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

InChI

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

SMILES string

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

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

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Legal Information

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

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.

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

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

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM5557
BCCK4580
BCCJ8019
BCCH1833
BCCJ0780

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
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
Reproductive toxicology. m-Nitrobenzoic acid.
Environmental health perspectives, 105 Suppl 1, 325-326 (1997-02-01)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service