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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)
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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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