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Elisartan CAS NO 149968-26-3
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CAS No.:149968-26-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Elisartan is a high-purity, non-peptide angiotensin II receptor antagonist (ARB) used as a key pharmaceutical intermediate. Its primary value lies in enabling the synthesis of advanced antihypertensive and cardiovascular APIs, offering a critical building block for modern drug development. This compound is essential for pharmaceutical manufacturers and R&D facilities focused on producing sartan-class medications for the global market.
Application
- Pharmaceutical Intermediate: Primary use in the synthesis of active pharmaceutical ingredients (APIs) for antihypertensive drugs.
- Angiotensin II Receptor Blocker (ARB) Development: Serves as a core scaffold for research and production of next-generation sartan medications.
- Cardiovascular Drug Research: Used in preclinical and clinical research for developing treatments for hypertension, heart failure, and diabetic nephropathy.
- Contract Manufacturing (CMO): Supplied to contract manufacturing organizations for large-scale API production under cGMP guidelines.
- Reference Standard: Can be utilized as a high-purity analytical reference standard for quality control and method validation.
- Academic & Institutional Research: Employed in biochemical and pharmacological studies investigating the renin-angiotensin system.
Basic Information
| Product Name | Elisartan |
| CAS No. | 149968-26-3 |
| Molecular Formula | C24H25N5O3 |
| Molecular Weight | 431.49 g/mol |
| Synonyms | 2-Butyl-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carboxylic acid; BIBR 277; BIBR-277; BIBR277; 1H-Benzimidazole-7-carboxylic acid, 2-butyl-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-; Telmisartan Impurity; Telmisartan Intermediate; BIBR 277 SE |
| EINECS | Contact for details |
Quality Control
Our Elisartan is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical synthesis. We provide comprehensive Certificates of Analysis (COA) detailing identity, purity, and impurity profiles, with specifications aligned with ICH guidelines. Quality is assured through advanced analytical techniques including HPLC, GC, and NMR.
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 powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Conforms to reference |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Loss on Drying | ≤ 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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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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