Cefathiamidine Impurity 4

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For Research Use Only | Not For Clinical Use

CAT	APB04624
Synonyms	2-bromo-N-((5aR,6R)-1,7-dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl)acetamide
Molecular Weight	333.16
Molecular Formula	C10H9BrN2O4S

What is the synonym for Cefathiamidine Impurity 4?

The synonym for Cefathiamidine Impurity 4 is 2-bromo-N-((5aR,6R)-1,7-dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl)acetamide.

What is the molecular weight of Cefathiamidine Impurity 4?

The molecular weight of Cefathiamidine Impurity 4 is 333.16.

What is the molecular formula of Cefathiamidine Impurity 4?

The molecular formula of Cefathiamidine Impurity 4 is C10H9BrN2O4S.

Is Cefathiamidine Impurity 4 a pure substance?

No, Cefathiamidine Impurity 4 is an impurity of Cefathiamidine.

What are the potential sources of Cefathiamidine Impurity 4 in the manufacturing process?

Potential sources of Cefathiamidine Impurity 4 in the manufacturing process could include reaction byproducts, degradation products, or impurities in raw materials.

How is Cefathiamidine Impurity 4 typically characterized in the pharmaceutical industry?

Cefathiamidine Impurity 4 is typically characterized through analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

What steps can be taken to minimize the formation of Cefathiamidine Impurity 4 during production?

Steps to minimize the formation of Cefathiamidine Impurity 4 may include optimizing reaction conditions, using high-quality starting materials, and implementing purification processes.

Why is it important to monitor and control impurities like Cefathiamidine Impurity 4 in pharmaceutical products?

Monitoring and controlling impurities like Cefathiamidine Impurity 4 is essential to ensure the safety, efficacy, and quality of pharmaceutical products.

What are the potential risks associated with high levels of impurities in pharmaceuticals?

High levels of impurities in pharmaceuticals can lead to decreased drug potency, unwanted side effects, and potential harm to patients.

How can regulatory agencies like the FDA impact the presence of impurities like Cefathiamidine Impurity 4 in pharmaceutical products?

Regulatory agencies like the FDA can set limits on impurity levels, require thorough testing and reporting of impurities, and enforce compliance with good manufacturing practices to ensure the quality of pharmaceutical products.

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