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Ceftazidime Hydrate CAS NO 120618-65-7
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CAS No.:120618-65-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Ceftazidime Hydrate CAS NO 120618-65-7 is a third-generation, broad-spectrum cephalosporin antibiotic. It is valued for its potent activity against a wide range of Gram-negative bacteria, including Pseudomonas aeruginosa. This product is essential for the synthesis of active pharmaceutical ingredients (APIs) in the pharmaceutical industry. It serves as a critical intermediate for manufacturers producing sterile injectable antibiotics for hospital use.
Application
- Pharmaceutical API Synthesis: Primary raw material for the manufacture of Ceftazidime for Injection, a vital antibiotic.
- Antibiotic Formulations: Used in the production of finished dosage forms, particularly for treating serious infections like pneumonia, sepsis, and meningitis.
- Hospital & Critical Care Medicine: A key component in drugs used for empiric therapy in immunocompromised patients and those with hospital-acquired infections.
- Research & Development: Serves as a reference standard and starting material in antimicrobial research and new drug development projects.
- Veterinary Pharmaceuticals: Employed in the development of antibiotic treatments for bacterial infections in animals.
Basic Information
| Product Name | Ceftazidime Hydrate |
| CAS No. | 120618-65-7 |
| Molecular Formula | C22H22N6O7S2 • xH2O |
| Molecular Weight | 546.58 (Anhydrous basis) |
| Synonyms | Ceftazidime; Ceftazidime Pentahydrate; GR-20263; Tazicef; Fortaz; Ceptaz; Spectrum; (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Glazidim |
| EINECS | Contact for details |
Quality Control
Our Ceftazidime Hydrate is produced under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical manufacturing. We provide comprehensive Certificates of Analysis (COA) that include data for identification, assay, impurity profile, and residual solvents, referencing pharmacopeial methodologies. Compliance with cGMP guidelines and relevant ICH stability protocols is maintained throughout production.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider conditions of 2-8°C.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to standard |
| Identification (HPLC) | Conforms to standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | 10.0% - 13.0% |
| pH (1% Solution) | 3.0 - 4.5 |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 2.0% |
| Residual Solvents (GC) | Meets 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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