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Key Documents

PHR1894

Supelco

Exemestane Related Compound A

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

6-Methyleneandrost-4-ene-3,17-dione

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About This Item

Formule empirique (notation de Hill):
C20H26O2
Numéro CAS:
Poids moléculaire :
298.42
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to USP 1269061

Famille d'API

exemestane

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

pkg of 30 mg

Application(s)

pharmaceutical

Format

neat

Température de stockage

2-8°C

InChI

1S/C20H26O2/c1-12-10-14-15-4-5-18(22)20(15,3)9-7-16(14)19(2)8-6-13(21)11-17(12)19/h11,14-16H,1,4-10H2,2-3H3/t14-,15-,16-,19+,20-/m0/s1

Clé InChI

KQRGETZTRARSMA-DAELLWKTSA-N

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Description générale

Exemestane Related Compound A is an impurity of the steroidal anticancer drug, exemestane. Exemestane belongs to the class of antiestrogens known as aromatase inhibitors. It is commonly used for the treatment of breast cancer.
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.

Application

Exemestane may be used as a pharmaceutical reference standard for the determination of the analyte in bulk drug and pharmaceutical formulations by chromatography.
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.

Remarque sur l'analyse

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

Autres remarques

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.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAB0339 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Pictogrammes

Health hazard

Mention d'avertissement

Warning

Mentions de danger

Conseils de prudence

Classification des risques

Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Development and validation of a stability indicating LC method for the assay and related substances determination of Exemestane, an aromatase inhibitor
Kumar RS, et al.
Journal of Pharmaceutical and Biomedical Analysis, 50(5), 746-752 (2009)
Analytical method validation for HPLC assay of oral anticancer drug exemestane
Yavuz B
FABAD Journal of Pharmaceutical Sciences, 32(1), 15-15 (2007)
Exemestane: a review of its clinical efficacy and safety
L?nning PE
Breast (Edinburgh, Scotland), 10(3), 198-208 (2001)
A novel validated stability-indicating RP-HPLC method for the determination of Exemestane (steroidal aromatase inhibitor)
Mukthinuthalapati MA and Bukkapatnam V
Journal of Bioequivalence & Bioavailability, 7(6), 288-288 (2015)

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