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About This Item
Linear Formula:
(C6H5)2CO
CAS Number:
Molecular Weight:
182.22
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1238185
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Carc. 1B - STOT RE 2 Oral
target_organs
Liver,Kidney
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
280.4 °F - closed cup
flash_point_c
138 °C - closed cup
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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
G Dormán et al.
Biochemistry, 33(19), 5661-5673 (1994-05-17)
The photoactivatable aryl ketone derivatives have been rediscovered as biochemical probes in the last 5 years. The expanding use of benzophenone (BP) photoprobes can be attributed to three distinct chemical and biochemical advantages. First, BPs are chemically more stable than
Global Trade Item Number
| SKU | GTIN |
|---|---|
| Y0000647 | 04061833804360 |