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Pregabalin Impurity 44

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For Research Use Only | Not For Clinical Use
CATAPB145328036
CAS145328-03-6
Molecular Weight216.28
Molecular FormulaC11H20O4

What is the product name of the compound with CAS number 145328-03-6?

The product name of the compound is Pregabalin Impurity 44.

What is the molecular weight of Pregabalin Impurity 44?

The molecular weight of Pregabalin Impurity 44 is 216.28.

What is the molecular formula of Pregabalin Impurity 44?

The molecular formula of Pregabalin Impurity 44 is C11H20O4.

What is the chemical structure of Pregabalin Impurity 44 based on its molecular formula?

The chemical structure of Pregabalin Impurity 44 based on its molecular formula is C11H20O4.

What is the significance of identifying Pregabalin Impurity 44 in pharmaceuticals?

Identifying Pregabalin Impurity 44 is important in pharmaceuticals to ensure the purity and quality of pregabalin medications.

How is Pregabalin Impurity 44 synthesized in the laboratory?

The synthesis of Pregabalin Impurity 44 in the laboratory involves specific chemical reactions using precursors and catalysts.

What are the potential impurities that may be present along with Pregabalin Impurity 44?

Potential impurities that may be present along with Pregabalin Impurity 44 could include related organic compounds or byproducts from the synthesis process.

How is Pregabalin Impurity 44 detected and quantified in pharmaceutical samples?

Pregabalin Impurity 44 can be detected and quantified in pharmaceutical samples using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or mass spectrometry.

What are the regulatory requirements regarding the presence of Pregabalin Impurity 44 in pharmaceutical formulations?

Regulatory bodies may have specific limits on the allowable concentration of Pregabalin Impurity 44 in pharmaceutical formulations to ensure safety and efficacy.

How does the presence of Pregabalin Impurity 44 affect the stability and shelf-life of medications?

The presence of Pregabalin Impurity 44 can affect the stability and shelf-life of medications by potentially causing degradation or undesired reactions over time.

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