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Sulfamethoxazole EP Impurity A

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For Research Use Only | Not For Clinical Use
CATAPB21312107
CAS21312-10-7
Structure
Molecular Weight295.31
Molecular FormulaC12H13N3O4S

What is the product name of the impurity defined by CAS 21312-10-7?

The product name is Sulfamethoxazole EP Impurity A.

What is the molecular weight of Sulfamethoxazole EP Impurity A?

The molecular weight is 295.31.

What is the molecular formula of Sulfamethoxazole EP Impurity A?

The molecular formula is C12H13N3O4S.

What does the "EP" in Sulfamethoxazole EP Impurity A stand for?

The "EP" stands for European Pharmacopoeia.

What is the significance of having impurities in pharmaceutical products?

Impurities in pharmaceutical products can affect the efficacy and safety of the medication.

How is Sulfamethoxazole EP Impurity A typically removed or reduced in pharmaceutical manufacturing?

Impurities like Sulfamethoxazole EP Impurity A can be removed or reduced through various purification processes during manufacturing.

Are impurities like Sulfamethoxazole EP Impurity A harmful to human health?

Impurities in pharmaceutical products can potentially be harmful to human health if present in high concentrations.

Does Sulfamethoxazole EP Impurity A have any known side effects or interactions with other drugs?

It's important to consult a healthcare professional or pharmacist for information on the side effects or interactions of Sulfamethoxazole EP Impurity A.

How is the purity of pharmaceutical products like Sulfamethoxazole EP Impurity A determined?

The purity of pharmaceutical products is typically determined through analytical testing methods such as chromatography.

What role does Sulfamethoxazole EP Impurity A play in the overall quality control of pharmaceutical products?

Sulfamethoxazole EP Impurity A is included in the quality control processes to ensure the purity and safety of the final pharmaceutical product.

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