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Eprosartan CAS NO 133040-01-4
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CAS No.:133040-01-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Eprosartan CAS NO 133040-01-4 is a potent and selective angiotensin II receptor antagonist (ARB) used as an active pharmaceutical ingredient (API). This compound is critical for the development and manufacture of antihypertensive medications, offering a targeted mechanism of action to manage high blood pressure. It is primarily required by pharmaceutical manufacturers, research institutions, and contract development and manufacturing organizations (CDMOs) involved in cardiovascular drug production.
Application
- Primary use as an Active Pharmaceutical Ingredient (API) in the formulation of antihypertensive drugs.
- Manufacturing of finished dosage forms, such as tablets and capsules, for the treatment of essential hypertension.
- Utilized in pharmaceutical research and development for studying angiotensin II receptor mechanisms.
- Reference standard in analytical laboratories for quality control and method validation.
- Used in preclinical and clinical studies to evaluate cardiovascular therapeutics.
- Sourcing for generic drug manufacturers producing cost-effective hypertension treatments.
Basic Information
| Product Name | Eprosartan |
| CAS No. | 133040-01-4 |
| Molecular Formula | C23H24N2O4S |
| Molecular Weight | 424.51 g/mol |
| Synonyms | Eprosartan; SKF-108566; (E)-3-[2-Butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazol-5-yl]-2-(2-thienylmethyl)propenoic Acid; Teveten (Brand Name); Eprosartan Mesylate (salt form); Angiotensin II Type 1 Receptor Antagonist; (E)-α-[[2-Butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazol-5-yl]methylene]-2-thiophenepropanoic Acid |
| EINECS | Contact for details |
Quality Control
Our Eprosartan is manufactured under strict quality systems to meet the rigorous standards of the pharmaceutical industry. Production adheres to current Good Manufacturing Practice (GMP) guidelines, and the material is typically characterized against relevant pharmacopeial monographs. A comprehensive Certificate of Analysis (COA), detailing purity, identity, and impurity profiles, is provided with each batch to ensure full traceability and compliance.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider conditions under an inert atmosphere.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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