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Merck

PHR1762

Supelco

奈韦拉平相关化合物C

Pharmaceutical Secondary Standard; Certified Reference Material

别名:

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

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About This Item

经验公式(希尔记法):
C15H16N4O
分子量:
268.31
分類程式碼代碼:
41116107
NACRES:
NA.24

等級

certified reference material
pharmaceutical secondary standard

品質等級

agency

traceable to USP 1460747

API 家族

nevirapine

CofA

current certificate can be downloaded

包裝

pkg of 50 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

pharmaceutical (small molecule)

格式

neat

儲存溫度

2-30°C

InChI

1S/C15H16N4O/c1-3-9-19-13-11(5-4-7-16-13)15(20)18-12-10(2)6-8-17-14(12)19/h4-8H,3,9H2,1-2H3,(H,18,20)

InChI 密鑰

YYEJELOKUZITDZ-UHFFFAOYSA-N

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一般說明

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 a member of the dipyridodiazepinone chemical class of compounds and is found to be the first antiretroviral agent, widely used for the treatment of adults and adolescents affected with human immunodeficiency viruses (HIV). Its mode of action involves slowing down damage to the immune system and suppresses the occurrence of AIDS-defining illnesses, via preventing HIV from replicating within cells by binding near reverse transcriptase′s active site and inhibiting polymerase activity

應用

Nevirapine may be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical samples using reversed-phase high-performance liquid chromatography technique.
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.

分析報告

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

其他說明

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.

腳註

To see an example of a Certificate of Analysis for this material enter LRAA8555 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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访问文档库

A simple and rapid RP-HPLC method for the estimation of nevirapine in bulk and pharmaceutical dosage forms
Mohanraj P, et al.
Journal of Chemistry, 5(S2), 1081-1086 (2008)
Identification, Isolation and Characterization of Unknown Acid Degradation Product of Nevirapine
Pottabathini V, et al.
American Journal of Analytical Chemistry, 7(09), 663-663 (2016)
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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