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Ingavirin CAS NO 219694-63-0
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CAS No.:219694-63-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Ingavirin is a synthetic, low-molecular-weight chemical compound with significant pharmacological interest. It matters as a key active pharmaceutical ingredient (API) and a valuable intermediate for advanced research and development. This product is primarily needed by pharmaceutical manufacturers, biotechnology research institutions, and chemical synthesis laboratories focused on antiviral and immunomodulatory therapeutics.
Application
- Active Pharmaceutical Ingredient (API): Primary use in the formulation of finished antiviral pharmaceutical products.
- Biomedical Research: Critical intermediate in preclinical and clinical studies investigating novel therapeutic agents.
- Chemical Synthesis: Serves as a key building block for the synthesis of more complex, targeted molecular entities.
- Reference Standard: Used as a high-purity standard in analytical laboratories for quality control and method development.
- Process Development: Employed in scaling up and optimizing manufacturing processes within GMP facilities.
Basic Information
| Product Name | Ingavirin |
| CAS No. | 219694-63-0 |
| Molecular Formula | C21H33N7O7 |
| Molecular Weight | 495.53 g/mol |
| Synonyms | Imidazolyl ethanamide pentanedioic acid; Dicarbonic acid, imidazolyl ethanamide derivative; 2-(2-Imidazol-5-ylethyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carboxylic acid; 1H-Isoindole-5-carboxylic acid, 2-(2-imidazol-5-ylethyl)-1,3-dihydro-1,3-dioxo-; Vitaglutam; Ingavirin (Trade Name); Antiviral agent R-1-3; UNII-7K3J8C8R2M |
| EINECS | Contact for details |
Quality Control
Our Ingavirin is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. We provide comprehensive quality documentation, including detailed Certificates of Analysis (COA) that confirm identity, purity, and conformance to agreed specifications. Our commitment to GMP principles and rigorous analytical testing ensures the material meets the high standards required for pharmaceutical development and manufacturing.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.5% |
| Related Substances (HPLC) | Total impurities ≤ 1.5% Any single impurity ≤ 0.5% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| 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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Why choose US
Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






