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Cefuroxime Sodium EP Impurity C is a chemical impurity found in the antibiotic drug cefuroxime sodium, which is used for treating bacterial infections. It is classified as an impurity due to its presence in small quantities, which can impact the purity and quality of the drug. As a degradation product of cefuroxime sodium, it is monitored and controlled during the manufacturing process to ensure the final product meets regulatory and safety standards. The presence and concentration of Cefuroxime Sodium EP Impurity C in the drug are analyzed using techniques such as chromatography and spectroscopy to guarantee the drug's safety and efficacy for medical use.

69822-88-4

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69822-88-4 Usage

Uses

Used in Pharmaceutical Manufacturing:
Cefuroxime Sodium EP Impurity C is used as a quality control parameter in the manufacturing process of cefuroxime sodium. It is monitored and controlled to ensure the purity and quality of the final drug product, meeting regulatory and safety standards.
Used in Drug Safety and Efficacy Analysis:
Cefuroxime Sodium EP Impurity C is used as an analytical target in methods such as chromatography and spectroscopy to determine its presence and concentration in the drug. This analysis helps ensure the safety and efficacy of cefuroxime sodium for medical use, preventing any potential adverse effects due to impurities.

Check Digit Verification of cas no

The CAS Registry Mumber 69822-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,2 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69822-88:
(7*6)+(6*9)+(5*8)+(4*2)+(3*2)+(2*8)+(1*8)=174
174 % 10 = 4
So 69822-88-4 is a valid CAS Registry Number.

69822-88-4Downstream Products

69822-88-4Relevant academic research and scientific papers

To carboxamide [...] preparation method (by machine translation)

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Paragraph 0015-0019, (2019/11/04)

The invention discloses a de-carboxamide [...] preparation method, which comprises: separately preparing 7 - ADCA of the inorganic alkali aqueous solution and is - [...] - 2 - furan acetyl chloride solution, then the acyl chloride solution is added 7 - ADCA aqueous solution, control pH7.0 - 8.0 reaction, after the reaction standstill phase separation, the aqueous phase is added in ethanol or methanol, then adding dichloromethane, then adjusting the pH to 2.0 standing after phase separation, the organic phase containing the product of the concentrated to viscous, water crystallization, filtration, washing, drying the product is obtained. Due to the direct the approach to the protection of the main raw materials [...] sodium salt of 7 - ADCA, eliminates the tedious organic compound protection, late stage can be avoided-protecting group of the tedious step again, simplifies the synthetic method, the conversion and yield of the product, the molar yield of 92%; by controlling the pH value of the condensation, the reaction by-product trans-acetyl [...] under control, the reaction end-content is less than 0.1%, thereby improving the purity of the product, the purity of the product can be improved to 98.5%. (by machine translation)

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