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Antigrippen CAS NO 76721-94-3


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CAS No.:76721-94-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Antigrippen CAS NO 76721-94-3 is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the efficacy and safety of final pharmaceutical formulations. It is primarily required by manufacturers in the pharmaceutical and fine chemical industries for the development and production of therapeutic agents.

Application

  • Pharmaceutical Synthesis: A key intermediate in the production of active pharmaceutical ingredients (APIs) for therapeutic use.
  • Antiviral Drug Development: Used in research and manufacturing of compounds targeting viral infections.
  • Fine Chemical Production: Serves as a building block for complex organic molecules in specialty chemical manufacturing.
  • Biochemical Research: Employed in laboratory settings for pharmacological studies and mechanism of action investigations.
  • Formulation Excipient: Can be utilized in the development of stable and bioavailable drug formulations.

Basic Information

Product Name Antigrippen
CAS No. 76721-94-3
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Antigrippin; 76721-94-3; Grippin; Anti-influenza compound; Antiviral intermediate; Pharmaceutical intermediate 76721-94-3
EINECS Contact for details

Quality Control

Our Antigrippen is produced under strict quality management systems. The product undergoes rigorous analytical testing to ensure it meets the high-purity standards required for pharmaceutical applications. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are available upon request to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider conditions recommended for light-sensitive pharmaceutical intermediates.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%

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

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