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Stavudine (Sodium) CAS NO 134624-73-0


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CAS No.:134624-73-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Stavudine (Sodium) is the sodium salt form of the nucleoside reverse transcriptase inhibitor (NRTI) stavudine. This compound is a critical active pharmaceutical ingredient (API) used in the formulation of antiretroviral medications. It is primarily required by pharmaceutical manufacturers and research institutions developing treatments for HIV/AIDS. The product is supplied to meet the stringent quality and regulatory standards of the global pharmaceutical industry.

Application

  • Active Pharmaceutical Ingredient (API) in the manufacture of antiretroviral drugs for HIV-1 infection.
  • Research and Development of novel antiviral therapies and combination drug formulations.
  • Reference Standard for analytical method development and quality control in pharmaceutical laboratories.
  • Pharmaceutical Intermediates for the synthesis of more complex drug substances or prodrugs.
  • Clinical Trial Material supply for studies investigating new treatment regimens.
  • Generic Drug Manufacturing for cost-effective antiviral medication production.

Basic Information

Product Name Stavudine (Sodium)
CAS No. 134624-73-0
Molecular Formula C10H11N2NaO4
Molecular Weight 246.20 g/mol
Synonyms Stavudine Sodium Salt; d4T Sodium Salt; 2',3'-Didehydro-3'-deoxythymidine Sodium Salt; Zerit® (Brand Name) Sodium Salt; BMY-27857 Sodium Salt; Stavudin Sodium; 1-((2R,5S)-5-(Hydroxymethyl)-2,5-dihydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione Sodium Salt
EINECS Contact for details

Quality Control

Our Stavudine (Sodium) is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and potency meet high-grade pharmaceutical standards. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with in-house specifications. We support customer audits and can provide documentation relevant to cGMP, ICH guidelines, and other major pharmacopoeial standards upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere packaging.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 5.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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