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A-145[Antiviral Drug] CAS NO 54805-04-8


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CAS No.:54805-04-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

A-145[Antiviral Drug] is a specialized active pharmaceutical ingredient (API) with the CAS registry number 54805-04-8. This compound is a critical intermediate or active component in the research and development of novel antiviral therapeutics. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on virology and infectious disease treatment. The material is supplied under stringent quality control to ensure consistency and reliability for demanding pharmaceutical applications.

Application

  • Pharmaceutical API Synthesis: Serves as a key building block or active moiety in the production of finished antiviral medications.
  • Antiviral Drug Research & Development: Used in preclinical and clinical research to study efficacy against specific viral pathogens.
  • Biochemical Assay Development: Employed as a reference standard or inhibitor in high-throughput screening and mechanism-of-action studies.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for scale-up and commercial production.
  • Academic Research: Utilized in university and institutional labs for virology and medicinal chemistry projects.

Basic Information

Product Name A-145[Antiviral Drug]
CAS No. 54805-04-8
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms A-145; A145; Antiviral Drug A-145; 54805-04-8; UNII-Contact for details; (Chemical name pending structure confirmation)
EINECS Contact for details

Quality Control

Our A-145[Antiviral Drug] is manufactured and tested under a quality management system designed for pharmaceutical intermediates. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency. Certificates of Analysis (COA) detailing specific results for assay, related substances, and residual solvents are provided with every shipment. We support compliance with cGMP and ICH Q7 guidelines for active pharmaceutical ingredients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Water Content (KF) ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C

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

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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

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

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.