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Merck
CN

B12407

4-Benzoylbenzoic acid

99%

Synonym(s):

p-Benzoylbenzoic acid, Benzophenone-4-carboxylic acid

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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
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Product Name

4-Benzoylbenzoic acid, 99%

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

mp

198-200 °C (lit.)

Quality Level

Gene Information

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Application

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

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Synthesis and luminescent properties of terbium complex containing 4-benzoylbenzoic acid for application in NUV-based LED.
Naiqun S
Journal of Rare Earths, 34(2), 130-136 (2016)
Antimicrobial and chemical detoxifying functions of cotton fabrics containing different benzophenone derivatives.
Hong K
Carbohydrate Polymers, 71(4), 598-605 (2008)
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)
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
N A Cacalano et al.
Journal of immunological methods, 118(2), 257-263 (1989-03-31)
Anti-cyclosporine antibodies were generated in rabbits, using an antigen derived from CsA. CsA was linked to carrier proteins by means of a photoactive cross-linking reagent, 4-benzoylbenzoic acid (BBa), an alpha, beta-unsaturated ketone. In the presence of CsA, photolysis of BBa

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