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461091

4-Nitrobenzoic acid

Name: 4-Nitrobenzoic acid
Brand: ALDRICH

98%

Synonym(s):

p-Nitrobenzoic acid

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About This Item

Linear Formula:

O₂NC₆H₄CO₂H

CAS Number:

62-23-7

Molecular Weight:

167.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24869806

EC Number:

200-526-2

Beilstein/REAXYS Number:

973593

MDL number:

MFCD00007352

Assay:

98%

Form:

solid

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Properties

Quality Level

200

assay

98%

form

solid

mp

237-240 °C (lit.)

functional group

carboxylic acid, nitro

SMILES string

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

InChI

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

InChI key

OTLNPYWUJOZPPA-UHFFFAOYSA-N

Description

General description

4-Nitrobenzoic acid (p-nitrobenzoic acid) is a carboxylic acid derivative. It participates in the biosynthesis of the antibiotic aureothin. Infrared Fourier transform spectroscopic studies suggest that the molecules of 4-nitrobenzoic acid gets adsorbed on the surfaces of fine silver powder as carboxylate.

Application

4-Nitrobenzoic acid may be used in the preparation of compounds (I and III) trans-M₂(T(i)PB)₂L₂, where T(i)PB = 2,4,6-triisopropylbenzoate:

compound I (L = 4-nitrobenzoate and M = Mo)
compound III (L = 4-nitrobenzoate and M₂ = MoW)

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pictograms

GHS08,GHS07

signalword

Warning

hcodes

H302,H315,H319,H341,H351,H361fd

pcodes

P202 - P264 - P301 + P312 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Diffuse reflectance infrared spectra of 4-nitrobenzoic acid and 4-cyanobenzoic acid self-assembled on fine silver particles.

Soo H, et al.

Applied Spectroscopy, 52(8) (1998)

4-Nitrophenyl- and 4'-nitro-1,1'-biphenyl-4-carboxylates attached to Mo2 quadruple bonds: ground versus excited state M2δ-ligand conjugation.

Brian G Alberding et al.

Dalton transactions (Cambridge, England : 2003), 43(29), 11397-11403 (2014-06-17)

From the reactions between Mo2(T(i)PB)4, where T(i)PB = 2,4,6-triisopropylbenzoate and two equivalents of the carboxylic acid LH (LH = 4-nitrobenzoic acid and 4'-nitro[1,1'-biphenyl]-4-carboxylic acid) the compounds trans-M2(T(i)PB)2L2 have been prepared: I (L = 4-nitrobenzoate and M = Mo), II (L

Characterization of the N-oxygenase AurF from Streptomyces thioletus.

Emmanuel Chanco et al.

Bioorganic & medicinal chemistry, 22(20), 5569-5577 (2014-06-30)

AurF catalyzes the N-oxidation of p-aminobenzoic acid to p-nitrobenzoic acid in the biosynthesis of the antibiotic aureothin. Here we report the characterization of AurF under optimized conditions to explore its potential use in biocatalysis. The pH optimum of the enzyme

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Global Trade Item Number

SKU	GTIN
461091-1KG	04061832344188
461091-250G	04061832344201