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Y0000647

Benzophenone

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Linear Formula:
(C6H5)2CO
CAS Number:
119-61-9
Molecular Weight:
182.22
Beilstein/REAXYS Number:
1238185
MDL number:
MFCD00003076
UNSPSC Code:
41116107
PubChem Substance ID:
329831072
NACRES:
NA.24

grade

pharmaceutical primary standard

agency

EP Reference Standard

vapor pressure

1 mmHg ( 108 °C)

API family

benzophenone

manufacturer/tradename

EDQM

bp

305 °C (lit.)

mp

47-51 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

O=C(C1=CC=CC=C1)C2=CC=CC=C2

InChI

1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

InChI key

RWCCWEUUXYIKHB-UHFFFAOYSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Benzophenone EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

related product

Product No.
Description
Pricing

pictograms

Health hazard
GHS08

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Carc. 1B - STOT RE 2 Oral

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

280.4 °F - closed cup

flash_point_c

138 °C - closed cup

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Sigma-Aldrich

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Masayuki Kyomoto et al.
Biomaterials, 34(32), 7829-7839 (2013-07-31)
We investigated the production of free radicals on a poly(ether-ether-ketone) (PEEK) substrate under ultraviolet (UV) irradiation. The amount of the ketyl radicals produced from the benzophenone (BP) units in the PEEK molecular structure initially increased rapidly and then became almost
Daniel Pockrandt et al.
Chembiochem : a European journal of chemical biology, 13(18), 2764-2771 (2012-11-15)
Gene-inactivation experiments have indicated that the putative prenyltransferase XptB from Aspergillus nidulans was likely to be responsible for the prenylation of 1,7-dihydroxy-6-methyl-8-hydroxymethylxanthone. Recently, it was suggested that this enzyme might also accept as substrate the benzophenone arugosin H, which is
Tao Zhang et al.
The Science of the total environment, 461-462, 49-55 (2013-05-29)
Limited information exists on the exposure of benzophenone (BP)-type UV filters (i.e., sunscreen compounds) in children, adults, and pregnant women in China. In this study, we determined the concentrations of five BP derivatives, BP-1, BP-2, BP-3, BP-8, and 4OH-BP in
Feifan Yu et al.
PloS one, 8(2), e56597-e56597 (2013-02-21)
Affinity proteins binding to antibody constant regions have proved to be invaluable tools in biotechnology. Here, protein engineering was used to expand the repertoire of available immunoglobulin binding proteins via improvement of the binding strength between the widely used staphylococcal
Ashna A Khan et al.
Organic & biomolecular chemistry, 11(6), 881-885 (2012-12-22)
Trehalose dimycolates (TDMs) are the most abundant glycolipids found in the cell wall of Mycobacterium tuberculosis (M. tb). TDMs play an important role in the pathogenesis of M. tb yet the only known receptor for TDM is the macrophage inducible
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