Skip to Content
Merck

B12407

4-Benzoylbenzoic acid

99%

Synonym(s):

p-Benzoylbenzoic acid, Benzophenone-4-carboxylic acid

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C6H5COC6H4CO2H
CAS Number:
Molecular Weight:
226.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-286-0
Beilstein/REAXYS Number:
1960224
MDL number:
Assay:
99%
Form:
crystals
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

InChI key

IFQUPKAISSPFTE-UHFFFAOYSA-N

InChI

1S/C14H10O3/c15-13(10-4-2-1-3-5-10)11-6-8-12(9-7-11)14(16)17/h1-9H,(H,16,17)

SMILES string

OC(=O)c1ccc(cc1)C(=O)c2ccccc2

assay

99%

form

crystals

Quality Level

Gene Information

Looking for similar products? Visit Product Comparison Guide

General description

4-Benzoylbenzoic acid is a benzophenone derivative. It can undergo hydrogenolysis to 4-benzylbenzoic acid. Cotton fabrics incorporated with 4-benzoylbenzoic acid have shown pesticide degradation ability, when exposed to UV irradiation.

Application

4-Benzoylbenzoic acid, along with methacrylic acid can be used as ligands for synthesizing a novel Tb(III) ternary complex with luminescent property.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

3-Mercapto-1, 2, 4-triazoles and N-acylated thiosemicarbazides as metallo-?-lactamase inhibitors.
Hussein W
Bioorganic & Medicinal Chemistry Letters, 22(1), 380-386 (2012)
K M Defife et al.
Journal of biomaterials science. Polymer edition, 10(10), 1063-1074 (1999-12-11)
Amphiphilic chains of 4-benzoylbenzoic acid moieties and polymer were photochemically immobilized onto silicone rubber to ask whether the covalently coupled polymers would passivate the silicone rubber by inhibiting protein adsorption and subsequent cell adhesion and activation. Three groups of polymers
K M DeFife et al.
Journal of biomedical materials research, 44(3), 298-307 (1999-07-09)
Photochemical immobilization technology was utilized to covalently couple polymers to silicone rubber either at multiple points along a polymer backbone or at the endpoint of an amphiphilic chain. The coating variants then were tested in vitro and in vivo for
Antimicrobial and chemical detoxifying functions of cotton fabrics containing different benzophenone derivatives.
Hong K
Carbohydrate Polymers, 71(4), 598-605 (2008)
G Scholz et al.
The Journal of biological chemistry, 264(8), 4318-4321 (1989-03-15)
4-Benzoylbenzoic acid inhibits pyridoxal kinase activity competitively with respect to pyridoxal. The Ki was determined to be 5 x 10(-5) M. Binding studies showed that 4-benzoylbenzoic acid bound to pyridoxal kinase at a 1:1 molar ratio and with a dissociation

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