Ofloxacin impurity E

EP Reference Standard

Reagent Code: #51350
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CAS Number 82419-52-1

science Other reagents with same CAS 82419-52-1

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Weight 347.34 g/mol
Formula C₁₇H₁₈FN₃O₄
badge Registry Numbers
MDL Number MFCD00871868
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description Product Description

Ofloxacin impurity E is primarily used in the pharmaceutical industry as a reference standard for quality control and analytical purposes. It helps in the identification, quantification, and validation of ofloxacin during its production process. This impurity is critical for ensuring the purity and efficacy of ofloxacin, a widely used antibiotic in the Fluoroquinolone group. By monitoring and controlling the levels of Ofloxacin impurity E, manufacturers can comply with regulatory standards and produce safer, high-quality pharmaceutical products. Additionally, it aids in research and development studies to understand the degradation pathways and stability of ofloxacin formulations.

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Size Availability Unit Price Quantity
inventory 20mg
10-20 days ฿22,563.00

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Ofloxacin impurity E
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Ofloxacin impurity E is primarily used in the pharmaceutical industry as a reference standard for quality control and analytical purposes. It helps in the identification, quantification, and validation of ofloxacin during its production process. This impurity is critical for ensuring the purity and efficacy of ofloxacin, a widely used antibiotic in the Fluoroquinolone group. By monitoring and controlling the levels of Ofloxacin impurity E, manufacturers can comply with regulatory standards and produce sa

Ofloxacin impurity E is primarily used in the pharmaceutical industry as a reference standard for quality control and analytical purposes. It helps in the identification, quantification, and validation of ofloxacin during its production process. This impurity is critical for ensuring the purity and efficacy of ofloxacin, a widely used antibiotic in the Fluoroquinolone group. By monitoring and controlling the levels of Ofloxacin impurity E, manufacturers can comply with regulatory standards and produce safer, high-quality pharmaceutical products. Additionally, it aids in research and development studies to understand the degradation pathways and stability of ofloxacin formulations.

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