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Documentos Principais

PHR1204

Supelco

Benzophenone

Pharmaceutical Secondary Standard; Certified Reference Material

Sinônimo(s):

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Fórmula linear:
(C6H5)2CO
Número CAS:
Peso molecular:
182.22
Beilstein:
1238185
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

certified reference material
pharmaceutical secondary standard

Nível de qualidade

Agency

traceable to Ph. Eur. Y0000647

pressão de vapor

1 mmHg ( 108 °C)

família API

benzophenone

Certificado de análise (CofA)

current certificate can be downloaded

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

p.e.

305 °C (lit.)

pf

47-51 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
pharmaceutical (small molecule)

Formato

neat

temperatura de armazenamento

2-30°C

cadeia de caracteres SMILES

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

chave InChI

RWCCWEUUXYIKHB-UHFFFAOYSA-N

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Descrição geral

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Benzophenone is widely used in the manufacture of cosmetics and pharmaceuticals for its UV rays absorbing and fragrance retention abilities. Due to its ability to absorb ultraviolet radiations harmful in the form of UVA (320-400 nm) and UVB (290-320 nm), it is effective against skin disorders and skin cancer. It is used in the synthesis of antihistamines, hypnotics, and insecticides and is present as a potential impurity in diphenhydramine hydrochloride, phenytoin bulk powder, and phenytoin dosage forms.

Aplicação

Benzophenone may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by chromatographic, spectrophotometric and polarographic techniques.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Nota de análise

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Outras notas

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Nota de rodapé

To see an example of a Certificate of Analysis for this material enter LRAC3932 in the slot below. This is an example certificate only and may not be the lot that you receive.

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogramas

Health hazard

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Liver,Kidney

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

280.4 °F - closed cup

Ponto de fulgor (°C)

138 °C - closed cup


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Certificados de análise (COA)

Lot/Batch Number

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Polarographic determination of phenytoin and benzophenone (as impurity) in pharmaceutical preparations
Razak OA, et al.
Journal of Pharmaceutical and Biomedical Analysis, 28(3-4), 613-619 (2002)
Derivative spectrophotometric analysis of benzophenone (as an impurity) in phenytoin
Walash MI, et al.
Chemistry Central Journal, 5(1), 85-85 (2011)
Separation and simultaneous high-performance liquid chromatographic determination of benzocaine and benzyl benzoate in a pharmaceutical preparation
Gigante Barbara, et al.
Journal of Chromatography A, 549(1), 217-220 (1991)
Simultaneous analysis of benzophenone sunscreen compounds in water sample by stir bar sorptive extraction with in situ derivatization and thermal desorption-gas chromatography-mass spectrometry
Kawaguchi M, et al.
Journal of Chromatography A, 1200(2), 260-263 (2008)
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

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