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PHR1761

Supelco

Nevirapine Related Compound B

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

5,11-Dihydro-4-methyl-6H-dipyrido[3,2-b:2′,3′-e][1,4]diazepin-6-one, 5,11-DIHYDRO-4-METHYL- 6H-DIPYRIDO[3,2-b:2’,3’-e][1,4] DIAZEPIN-6-ONE

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About This Item

Formule empirique (notation de Hill):
C12H10N4O
Numéro CAS:
Poids moléculaire :
226.23
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to USP 1460736

Famille d'API

nevirapine

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

pkg of 50 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-30°C

InChI

1S/C12H10N4O/c1-7-4-6-14-11-9(7)15-12(17)8-3-2-5-13-10(8)16-11/h2-6H,1H3,(H,15,17)(H,13,14,16)

Clé InChI

RKCRKBSFEVQVSX-UHFFFAOYSA-N

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Description générale

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. Nevirapine is found to be the first antiretroviral agent and selective non-competitive inhibitor of the reverse transcriptase, widely used for the treatment of adults and adolescents affected with human immunodeficiency viruses (HIV).

Application

Nevirapine may be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical samples using capillary zone electrophoresis method.
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 LRAA8554 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Pictogrammes

Skull and crossbones

Mention d'avertissement

Danger

Mentions de danger

Conseils de prudence

Classification des risques

Acute Tox. 3 Oral

Code de la classe de stockage

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

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)

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Consulter la Bibliothèque de documents

Development and validation of a simple and rapid capillary zone electrophoresis method for determination of nnrti nevirapine in pharmaceutical formulations
Filho ZAL, et al.
Journal of the Brazilian Chemical Society, 22(10), 205-2012 (2011)
Simultaneous determination of zidovudine and nevirapine in human plasma by RP-LC
Marchei E, et al.
Journal of Pharmaceutical and Biomedical Analysis, 29(6), 1081-1088 (2002)
Development of a liposomal nanodelivery system for nevirapine
Ramana NL, et al.
Journal of Biomedical Science, 17(1), 57-57 (2010)

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