Leflunomide impurity 1

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For Research Use Only | Not For Clinical Use

CAT	APB61643230
CAS	61643-23-0
Structure
Molecular Weight	270.21
Molecular Formula	C12H9F3N2O2

What is the name of the impurity with CAS number 61643-23-0?

The name of the impurity is Leflunomide impurity 1.

What is the molecular weight of Leflunomide impurity 1?

The molecular weight of Leflunomide impurity 1 is 270.21.

What is the molecular formula of Leflunomide impurity 1?

The molecular formula of Leflunomide impurity 1 is C12H9F3N2O2.

How is Leflunomide impurity 1 different from the main compound leflunomide?

Leflunomide impurity 1 is a separate impurity with a different chemical structure and molecular formula compared to the main compound leflunomide.

What role does Leflunomide impurity 1 play in pharmaceutical production?

Leflunomide impurity 1 may be monitored and controlled during pharmaceutical production to ensure the quality and purity of the final product.

Are impurities like Leflunomide impurity 1 typically harmful or beneficial in pharmaceuticals?

Impurities like Leflunomide impurity 1 are generally considered undesirable in pharmaceuticals because they may affect the safety and efficacy of the drug.

How can the presence of Leflunomide impurity 1 be detected in a pharmaceutical product?

Analytical techniques such as chromatography and spectroscopy can be used to detect and quantify Leflunomide impurity 1 in a pharmaceutical product.

Is Leflunomide impurity 1 a common impurity found in leflunomide-based medications?

Leflunomide impurity 1 may be a common impurity found in leflunomide-based medications, but its presence should be minimized to ensure product quality.

What precautions should be taken during the manufacturing process to prevent the formation of Leflunomide impurity 1?

Manufacturers may implement strict quality control measures, use high purity raw materials, and optimize reaction conditions to minimize the formation of Leflunomide impurity 1.

Can Leflunomide impurity 1 be removed from a pharmaceutical product once it has formed?

It may be challenging to remove Leflunomide impurity 1 once it has formed, but steps can be taken to reduce its concentration to acceptable levels in the final product.

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