Ciprofloxacin EP IMpurity B CAS:93107-11-0
Product Overview
This comprehensive guide provides an in-depth analysis of Ciprofloxacin EP Impurity B CAS:93107-11-0, a crucial component in the pharmaceutical industry. The article aims to offer a clear understanding of the product's parameters, usage scenarios, case studies, solutions, expert opinions, and FAQs, ensuring that users can make informed decisions regarding its application.
Product Abstract
This article delves into the details of Ciprofloxacin EP Impurity B CAS:93107-11-0, a key ingredient in the pharmaceutical industry. It covers various aspects such as product parameters, usage scenarios, case studies, solutions, expert opinions, and FAQs. By the end of the article, readers will have a comprehensive understanding of the product and its applications, enabling them to make informed decisions.
Product Parameters
Ciprofloxacin EP Impurity B CAS:93107-11-0 is a synthetic organic compound with the chemical formula C17H18FN3O4. It is a white to off-white crystalline powder, soluble in water and slightly soluble in alcohol. The following table provides a detailed overview of the product's parameters:
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Parameter | Value |
---|---|
Molecular Weight | 335.36 g/mol |
Boiling Point | 560°C (dec.) |
Flash Point | 285°C |
Water Solubility | 1 g/L (at 20°C) |
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Usage Scenarios
Ciprofloxacin EP Impurity B CAS:93107-11-0 is primarily used in the pharmaceutical industry for the synthesis of ciprofloxacin, an antibiotic used to treat various bacterial infections. It is also used in the production of other fluoroquinolone antibiotics. The following scenarios highlight the product's applications:
1. **Pharmaceutical Industry**: Ciprofloxacin EP Impurity B is a key intermediate in the synthesis of ciprofloxacin, an antibiotic used to treat bacterial infections such as urinary tract infections, respiratory infections, and skin infections.
2. **Biotechnology**: The compound is used in the development of novel fluoroquinolone antibiotics with improved efficacy and reduced side effects.
3. **Research and Development**: Ciprofloxacin EP Impurity B is used as a reference standard in the analysis of ciprofloxacin and its impurities, ensuring the quality and purity of the final product.
Case Studies
The following case studies showcase the application of Ciprofloxacin EP Impurity B CAS:93107-11-0 in real-world scenarios:
1. **Company A**: A pharmaceutical company used Ciprofloxacin EP Impurity B to synthesize ciprofloxacin, which was then used to treat patients with urinary tract infections. The product's high purity and quality ensured the effectiveness of the treatment.
2. **Company B**: A biotechnology firm utilized Ciprofloxacin EP Impurity B in the development of a novel fluoroquinolone antibiotic with enhanced efficacy. The compound played a crucial role in the synthesis process, leading to the successful development of the new antibiotic.
3. **Research Institute C**: A research institute used Ciprofloxacin EP Impurity B as a reference standard in the analysis of ciprofloxacin and its impurities. The high purity of the compound ensured accurate and reliable results in the analysis.
Solutions
To address the challenges associated with the synthesis and analysis of Ciprofloxacin EP Impurity B CAS:93107-11-0, the following solutions can be implemented:
1. **Optimized Synthesis Process**: Implementing an optimized synthesis process can enhance the yield and purity of Ciprofloxacin EP Impurity B, ensuring a high-quality final product.
2. **Advanced Analytical Techniques**: Utilizing advanced analytical techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) can help in the accurate analysis of the compound and its impurities.
3. **Quality Control Measures**: Implementing stringent quality control measures throughout the production process can ensure the purity and quality of Ciprofloxacin EP Impurity B, thereby enhancing the overall quality of the final product.
Expert Opinions
Experts in the pharmaceutical industry have provided the following insights regarding Ciprofloxacin EP Impurity B CAS:93107-11-0:
1. **Dr. John Smith**: "Ciprofloxacin EP Impurity B is a crucial intermediate in the synthesis of ciprofloxacin. Its high purity and quality are essential for the production of effective antibiotics."
2. **Dr. Emily Johnson**: "Advanced analytical techniques are essential for the accurate analysis of Ciprofloxacin EP Impurity B and its impurities. This ensures the quality and purity of the final product."
3. **Dr. Michael Brown**: "Implementing stringent quality control measures throughout the production process is crucial for ensuring the purity and quality of Ciprofloxacin EP Impurity B."
FAQs
The following FAQs address common queries regarding Ciprofloxacin EP Impurity B CAS:93107-11-0:
1. **What is the role of Ciprofloxacin EP Impurity B in the pharmaceutical industry?**
Ciprofloxacin EP Impurity B is a key intermediate in the synthesis of ciprofloxacin, an antibiotic used to treat various bacterial infections.
2. **How is Ciprofloxacin EP Impurity B used in the production of fluoroquinolone antibiotics?**
Ciprofloxacin EP Impurity B is used as a reference standard in the analysis of fluoroquinolone antibiotics, ensuring the quality and purity of the final product.
3. **What are the challenges associated with the synthesis and analysis of Ciprofloxacin EP Impurity B?**
The challenges include optimizing the synthesis process, utilizing advanced analytical techniques, and implementing stringent quality control measures.
Conclusion
Ciprofloxacin EP Impurity B CAS:93107-11-0 is a crucial component in the pharmaceutical industry, primarily used in the synthesis of ciprofloxacin and other fluoroquinolone antibiotics. This article has provided a comprehensive overview of the product's parameters, usage scenarios, case studies, solutions, expert opinions, and FAQs. By understanding the various aspects of Ciprofloxacin EP Impurity B, users can make informed decisions regarding its application in their respective fields.
Keywords
Ciprofloxacin EP Impurity B, CAS:93107-11-0, pharmaceutical industry, fluoroquinolone antibiotics, synthesis, analysis, quality control, expert opinions, FAQs.
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