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Zoledronic Acid CAS NO 1334703-07-9
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CAS No.:1334703-07-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Zoledronic Acid CAS NO 1334703-07-9 is a high-potency bisphosphonate compound, serving as the active pharmaceutical ingredient (API) for the treatment of bone-related disorders. Its primary value lies in its superior efficacy in inhibiting osteoclast-mediated bone resorption, making it a critical component in advanced pharmaceutical formulations. This product is essential for manufacturers in the global pharmaceutical industry developing treatments for osteoporosis, hypercalcemia of malignancy, and Paget's disease of bone.
Application
- Primary Active Pharmaceutical Ingredient (API) in injectable formulations for osteoporosis treatment.
- Key component in oncology-supportive care drugs for managing skeletal-related events and hypercalcemia of malignancy.
- Used in the research and development of novel bone-targeting therapeutic agents and drug delivery systems.
- Essential raw material for compounding pharmacies and specialty pharmaceutical manufacturers.
- Reference standard in analytical laboratories for quality control and method validation of bisphosphonate drugs.
- Intermediate in the synthesis of more complex, bone-specific radiopharmaceuticals and diagnostic agents.
Basic Information
| Item | Details |
|---|---|
| Product Name | Zoledronic Acid |
| CAS No. | 1334703-07-9 |
| Molecular Formula | C5H10N2O7P2 |
| Molecular Weight | 272.09 g/mol |
| Synonyms | Zoledronate; Zoledronic Acid Monohydrate; CGP 42446; (1-Hydroxy-2-imidazol-1-yl-phosphonoethyl)phosphonic acid; Zometa (trade name); Reclast (trade name); Aclasta (trade name); IUPAC: (1-Hydroxy-2-(1H-imidazol-1-yl)ethane-1,1-diyl)bis(phosphonic acid) |
| EINECS | Contact for details |
Quality Control
Our Zoledronic Acid is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity pharmaceutical standards, with specifications aligned with major pharmacopoeial requirements. A detailed Certificate of Analysis (COA), documenting identity, purity, and impurity profiles, is provided with every shipment to guarantee traceability and compliance.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a low-humidity environment to prevent degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 1.0% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any individual impurity ≤ 0.5% |
| Residual Solvents (GC) | Meets ICH Q3C guidelines |
| Heavy Metals | ≤ 20 ppm |
| pH (1% Solution) | 2.0 - 3.0 |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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