Azilsartan Impurity 107

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For Research Use Only | Not For Clinical Use

CAT	APB91526168
CAS	91526-16-8
Synonyms	(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-methylbenzenesulfonate
Molecular Weight	284.29
Molecular Formula	C12H12O6S

What is the product name of CAS 91526-16-8?

The product name is Azilsartan Impurity 107.

What are the synonyms for Azilsartan Impurity 107?

One of the synonyms is (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-methylbenzenesulfonate.

What is the molecular weight of Azilsartan Impurity 107?

The molecular weight is 284.29.

What is the molecular formula of Azilsartan Impurity 107?

The molecular formula is C12H12O6S.

What is the chemical structure of Azilsartan Impurity 107?

The chemical structure is characterized by a 5-methyl-2-oxo-1,3-dioxol-4-yl group attached to a 4-methylbenzenesulfonate group.

What is the significance of Azilsartan Impurity 107 in relation to drug development?

Azilsartan Impurity 107 is an impurity found in the drug Azilsartan, and its identification and quantification are important in ensuring the purity and safety of the drug.

How is Azilsartan Impurity 107 typically detected and analyzed?

Azilsartan Impurity 107 is typically detected and analyzed using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

What is the potential impact of Azilsartan Impurity 107 on the efficacy of Azilsartan as a drug?

The presence of impurities such as Azilsartan Impurity 107 may affect the efficacy and safety of Azilsartan as a drug, highlighting the importance of monitoring and controlling impurity levels.

Are there specific regulations or guidelines related to the presence of Azilsartan Impurity 107 in pharmaceutical products?

There may be specific regulations or guidelines set by regulatory authorities regarding the acceptable levels of Azilsartan Impurity 107 in pharmaceutical products to ensure patient safety and product quality.

How might the synthesis and production process of Azilsartan be optimized to minimize the formation of Azilsartan Impurity 107?

Optimizing the synthesis and production process of Azilsartan may involve using higher purity starting materials, controlling reaction conditions, and implementing purification techniques to minimize the formation of impurities like Azilsartan Impurity 107.

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