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Y0000647

Benzophenone

European Pharmacopoeia (EP) Reference Standard

Sinonimo/i:

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Formula condensata:
(C6H5)2CO
Numero CAS:
119-61-9
Peso molecolare:
182.22
Beilstein:
1238185
Numero MDL:
MFCD00003076
Codice UNSPSC:
41116107
ID PubChem:
329831072
NACRES:
NA.24

Grado

pharmaceutical primary standard

agenzia

EP Reference Standard

Tensione di vapore

1 mmHg ( 108 °C)

Famiglia di API

benzophenone

Produttore/marchio commerciale

EDQM

P. eboll.

305 °C (lit.)

Punto di fusione

47-51 °C (lit.)

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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
RWCCWEUUXYIKHB-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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

Confezionamento

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

Altre note

Sales restrictions may apply.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

Health hazard
GHS08

Avvertenze

Danger

Indicazioni di pericolo

H350,H373,H412

Classi di pericolo

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

Organi bersaglio

Liver,Kidney

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

280.4 °F - closed cup

Punto d’infiammabilità (°C)

138 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number

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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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