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Palbociclib Impurity 39

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For Research Use Only | Not For Clinical Use
CATAPB2242625369
CAS2242625-36-9
Molecular Weight281.74
Molecular FormulaC13H16ClN3O2

What is the product name of the compound with CAS number 2242625-36-9?

The product name is Palbociclib Impurity 39.

What is the molecular weight of Palbociclib Impurity 39?

The molecular weight is 281.74.

What is the molecular formula of Palbociclib Impurity 39?

The molecular formula is C13H16ClN3O2.

How is Palbociclib Impurity 39 classified based on its molecular formula?

It is classified as an organic compound containing carbon, hydrogen, chlorine, nitrogen, and oxygen atoms.

What is the significance of identifying impurities in pharmaceutical compounds like Palbociclib?

Identifying impurities is important for ensuring the safety, efficacy, and quality of pharmaceutical products.

How is Palbociclib Impurity 39 different from the main active ingredient Palbociclib?

Palbociclib Impurity 39 is a related compound or impurity found in the synthesis or production of Palbociclib, but it is not the main active ingredient in the drug.

How can Palbociclib Impurity 39 affect the potency or stability of the final drug product?

Impurities like Palbociclib Impurity 39 can potentially affect the potency, stability, and overall quality of the final drug product if present in high concentrations.

What are some methods used to detect and quantify impurities in pharmaceutical compounds?

Methods such as chromatography, spectroscopy, and mass spectrometry are commonly used to detect and quantify impurities in pharmaceutical compounds.

How can the presence of impurities like Palbociclib Impurity 39 be controlled during the manufacturing process?

Strict quality control measures, purification techniques, and process optimization can help control and minimize the presence of impurities in pharmaceutical manufacturing.

What regulatory guidelines address the acceptable levels of impurities in pharmaceutical products like Palbociclib?

Regulatory bodies like the FDA and EMA have specific guidelines and limits for impurities in pharmaceutical products to ensure patient safety and product quality.

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