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PHR1292

Supelco

Zidovudine

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

3′-Azido-3′-deoxythymidine, AZT, Azidothymidine, ZDV, Zidovudine

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About This Item

Formula empirica (notazione di Hill):
C10H13N5O4
Numero CAS:
Peso molecolare:
267.24
Beilstein:
3595791
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

certified reference material
pharmaceutical secondary standard

Livello qualitativo

agenzia

traceable to BP 803
traceable to Ph. Eur. Z1900000
traceable to USP 1724500

Famiglia di API

zidovudine

CdA

current certificate can be downloaded

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

113-115 °C (lit.)

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O

InChI

1S/C10H13N5O4/c1-5-3-15(10(18)12-9(5)17)8-2-6(13-14-11)7(4-16)19-8/h3,6-8,16H,2,4H2,1H3,(H,12,17,18)/t6-,7+,8+/m0/s1
HBOMLICNUCNMMY-XLPZGREQSA-N

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Descrizione generale

Zidovudine (AZT) is a thymidine analog anti-HIV drug, known to decrease the mortality rate in patients affected with HIV. The mode of action involves inhibiting the activity of viral reverse transcriptase and interrupting HIV replication.

Certified pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to in-house working standards.

Applicazioni

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.
Zidovudine may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations, tablets and drug dosage forms by chromatography and spectrophotometric techniques.

Azioni biochim/fisiol

Reverse transcriptase inhibitor active against HIV-1 virus.

Risultati analitici

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

Altre note

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 a piè di pagina

To see an example of a Certificate of Analysis for this material enter LRAA0303 in the slot below. This is an example certificate only and may not be the lot that you receive.

Pittogrammi

Health hazard

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Carc. 2 - Muta. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Lamivudine ≥98% (HPLC), powder

Sigma-Aldrich

L1295

Lamivudine

vibrant-m

Z1904000

Zidovudine impurity B

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Reverse Phase High Performance Liquid Chromatographic Determination Of Zidovudine And Lamivudine In Tablet Dosage Form.
Palled MS, et al.
Indian Journal of Pharmaceutical Sciences, 67(1), 110-110 (2005)
Photoelectron spectra of important drug molecules: Zidovudine and Artemisinine
Novak I and Kovac B
The Journal of Organic Chemistry, 68(14), 5777-5779 (2003)
Spectrophotometric determination of Zidovudine in pharmaceuticals based on charge-transfer complexation involving N-bromosuccinimide, metol and sulphanilic acid as reagents
Basavaiah K, et al.
Journal of Chemistry, 4(2), 173-179 (2007)
Simultaneous determination of HIV-protease inhibitors lamivudine and zidovudine in pharmaceutical formulations by micellar electrokinetic chromatography
Sekar R and Azhaguvel S
Journal of Pharmaceutical and Biomedical Analysis, 39(3-4), 653-660 (2005)
Alteration of zidovudine pharmacokinetics by probenecid in patients with AIDS or AIDS-related complex
de Miranda P, et al.
Clinical Pharmacology and Therapeutics, 46(5), 494-499 (1989)

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