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Sumatriptan EP Impurity E

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For Research Use Only | Not For Clinical Use
CATAPB88919226
CAS88919-22-6
Structure
Molecular Weight267.35
Molecular FormulaC12H17N3O2S

What is the product name of the compound with CAS number 88919-22-6?

The product name is Sumatriptan EP Impurity E.

What is the molecular weight of Sumatriptan EP Impurity E?

The molecular weight is 267.35.

What is the molecular formula of Sumatriptan EP Impurity E?

The molecular formula is C12H17N3O2S.

Is Sumatriptan EP Impurity E a pure substance or an impurity?

It is an impurity of Sumatriptan.

What does EP stand for in Sumatriptan EP Impurity E?

EP stands for European Pharmacopoeia.

What are the possible sources of Sumatriptan EP Impurity E in pharmaceutical manufacturing?

Sumatriptan EP Impurity E can be a result of degradation of Sumatriptan or impurities in starting materials.

How can Sumatriptan EP Impurity E be detected and quantified in pharmaceutical products?

It can be detected and quantified using analytical techniques such as HPLC (High Performance Liquid Chromatography) or mass spectrometry.

What impact can the presence of Sumatriptan EP Impurity E have on the quality and safety of pharmaceutical products?

The presence of impurities like Sumatriptan EP Impurity E can affect the potency, stability, and safety of the pharmaceutical products.

How can the levels of Sumatriptan EP Impurity E be controlled during the manufacturing process?

Control strategies such as using high-quality starting materials, optimizing synthesis conditions, and implementing purification steps can help control impurity levels.

Are there specific regulatory limits for Sumatriptan EP Impurity E in pharmaceutical products?

Regulatory agencies may have specific limits or guidelines regarding the acceptable levels of Sumatriptan EP Impurity E in pharmaceutical products.

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