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Palbociclib Impurity G

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For Research Use Only | Not For Clinical Use
CATAPB2377610256
CAS2377610-25-6
Molecular Weight299.1
Molecular FormulaC11H21BF3NO4

What is the product name of the listed chemical compound?

The product name of the listed chemical compound is Palbociclib Impurity G.

What is the CAS number of Palbociclib Impurity G?

The CAS number of Palbociclib Impurity G is 2377610-25-6.

What is the molecular weight of Palbociclib Impurity G?

The molecular weight of Palbociclib Impurity G is 299.1.

What is the molecular formula of Palbociclib Impurity G?

The molecular formula of Palbociclib Impurity G is C11H21BF3NO4.

What is the chemical structure of Palbociclib Impurity G?

The chemical structure of Palbociclib Impurity G is C11H21BF3NO4.

What is the significance of identifying impurities in pharmaceutical compounds?

Identifying impurities in pharmaceutical compounds is crucial for ensuring the safety and efficacy of the final drug product.

How is Palbociclib Impurity G typically detected and analyzed in pharmaceutical manufacturing processes?

Palbociclib Impurity G is typically detected and analyzed using techniques such as chromatography and spectroscopy in pharmaceutical manufacturing processes.

Are there specific guidelines or limits for the presence of Palbociclib Impurity G in pharmaceutical formulations?

Yes, there are usually specific guidelines or limits set by regulatory authorities for the presence of impurities like Palbociclib Impurity G in pharmaceutical formulations.

How can Palbociclib Impurity G impact the stability and quality of a pharmaceutical product?

Palbociclib Impurity G can potentially impact the stability and quality of a pharmaceutical product by altering its chemical composition or properties.

What steps can be taken to minimize or eliminate the presence of Palbociclib Impurity G in pharmaceutical production?

To minimize or eliminate the presence of Palbociclib Impurity G in pharmaceutical production, manufacturers can implement strict quality control measures, optimize production processes, and conduct thorough impurity testing and analysis.

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