213672-25-4 Usage
Uses
Used in Pharmaceutical Industry:
GeMifloxacin IMpurity is used as a reference material for the development and validation of analytical methods in the pharmaceutical industry. Its application is crucial for ensuring the quality, safety, and efficacy of Gemifloxacin, a widely prescribed antibiotic for various bacterial infections.
GeMifloxacin IMpurity is used as a quality control substance for [application reason] in the pharmaceutical industry. The application reason is to ensure the accurate identification, quantification, and control of impurities in the manufacturing process of Gemifloxacin, thereby maintaining the desired quality and potency of the final product.
Used in Research and Development:
GeMifloxacin IMpurity is used as a research tool for studying the chemical and pharmacological properties of Gemifloxacin and its related compounds. Its application in research and development helps scientists and researchers to better understand the structure-activity relationship, potential side effects, and mechanisms of action of the parent drug.
GeMifloxacin IMpurity is used as a research compound for [application reason] in the field of medicinal chemistry and pharmacology. The application reason is to facilitate the investigation of the drug's properties, interactions, and potential applications in various therapeutic areas, ultimately contributing to the advancement of new and improved treatments for bacterial infections.
Used in Regulatory Compliance:
GeMifloxacin IMpurity is used as a regulatory reference standard for assessing the compliance of Gemifloxacin with international quality standards and guidelines. Its application in regulatory compliance ensures that the drug meets the required specifications and is safe for use in the treatment of bacterial infections.
GeMifloxacin IMpurity is used as a regulatory standard for [application reason] in the pharmaceutical industry. The application reason is to verify the identity, purity, and concentration of the drug and its impurities, ensuring that the manufacturing process adheres to the established quality standards and guidelines, and that the final product is safe and effective for its intended use.
Check Digit Verification of cas no
The CAS Registry Mumber 213672-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 213672-25:
(8*2)+(7*1)+(6*3)+(5*6)+(4*7)+(3*2)+(2*2)+(1*5)=114
114 % 10 = 4
So 213672-25-4 is a valid CAS Registry Number.