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Moxifloxacin HCL BP
Moxifloxacin HCL BP Specification
- Extraction Type
- Synthetic
- Smell
- Odourless
- Odour
- Odourless
- EINECS No
- Not listed
- Loss on Drying
- Not more than 1.0%
- Storage
- Store in a cool, dry place, protected from light
- Boiling point
- Not available (decomposes)
- Shelf Life
- 24 months from date of manufacture
- Poisonous
- No (if used as directed)
- Ph Level
- Neutral to slightly acidic
- Melting Point
- 238-242C (decomposes)
- Solubility
- Freely soluble in water, slightly soluble in methanol, practically insoluble in acetone and ether
- Taste
- Bitter
- Molecular Formula
- C21H24FN3O4HCl
- Structural Formula
- Available upon request (see reference structure)
- Molecular Weight
- 437.90 g/mol (free base)
- HS Code
- 29419090
- Color
- Off-white to pale yellow
- Heavy Metal (%)
- 20 ppm
- Particle Size
- Standard and micronized grades available
- Medicine Name
- Moxifloxacin HCL BP
- Chemical Name
- Moxifloxacin hydrochloride
- CAS No
- 186826-86-8
- Type
- Active Pharmaceutical Ingredient (API)
- Grade
- BP (British Pharmacopoeia)
- Usage
- Used as an antibacterial agent in pharmaceutical formulations
- Purity(%)
- >= 98%
- Appearance
- Off-white to light yellow powder
- Physical Form
- Solid/Powder
- Packing Details
- Packed in fiber drums of 25kg net or as per client requirements
- Assay (on dry basis)
- 98% and 102%
- Identification
- IR & UV conform to reference standard
- Bacterial Endotoxins
- < 0.5 IU/mg
- Microbial Limit
- Complies with pharmacopeial requirements
- pH of 1% solution
- 4.0 - 6.5
- Residual Solvents
- Complies with ICH guidelines
- Application
- For oral and injectable antibiotic formulations
- Chloride Content
- Conforms to standard
- Related Substances
- Not more than 0.2% for unidentified impurities
About Moxifloxacin HCL BP
Distinctive Features and Broad Applications
Moxifloxacin HCL BP features a neutral to slightly acidic pH, outstanding solubility in water, and compliance with the strictest residual solvent and endotoxin requirements. It is odourless, bitter-tasting, and available in standard and micronized particle sizes. Primarily used as an antibacterial agent in oral and injectable formulations, it is also valuable for developing advanced pharmaceutical solutions aimed at resistant microbial infections, reflecting its versatile and robust application profile.
Export Markets, Supply Terms, and Delivery Details
Our heroic supply of Moxifloxacin HCL BP reaches main export markets across Europe, Asia, the Middle East, Africa, and the Americas. Shipments are processed promptly, usually delivered within weeks depending on the proposal amount and client requirements. Payment terms are flexible and structured for client convenience, ensuring seamless transactions. Each batch is meticulously packed in 25 kg fiber drums or per request, ensuring shipped goods maintain peak freshness throughout transit.
FAQ's of Moxifloxacin HCL BP:
Q: How is Moxifloxacin HCL BP primarily used in pharmaceutical formulations?
A: Moxifloxacin HCL BP is used as an antibacterial agent in both oral and injectable pharmaceutical formulations, addressing a wide spectrum of microbial infections.Q: What benefits does Moxifloxacin HCL BP offer regarding quality and compliance?
A: Moxifloxacin HCL BP provides assured purity (98%), low unidentified impurities, and strict adherence to ICH and BP guidelines, ensuring rarefied safety and efficacy in pharmaceutical applications.Q: When can I expect delivery after my order is placed?
A: Delivery times are prompt, with most orders shipped within a few weeks after confirming the proposal amount and payment terms, ensuring efficient and reliable supply chains.Q: Where should Moxifloxacin HCL BP be stored for optimal quality?
A: For best results, store Moxifloxacin HCL BP in a cool, dry place protected from light, preserving its freshness and physicochemical integrity for up to 24 months.Q: What is the process for verifying the identification and purity of this API?
A: Identification is confirmed by IR & UV methods, and purity is validated using BP standards, including comprehensive impurity profiling and compliance with international pharmacopoeial requirements.

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