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Levosimendan Impurity 10

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For Research Use Only | Not For Clinical Use
CATAPB220246811
CAS220246-81-1
Structure
Molecular Weight245.28
Molecular FormulaC13H15N3O2

What is the product name of CAS 220246-81-1?

The product name is Levosimendan Impurity 10.

What is the molecular weight of Levosimendan Impurity 10?

The molecular weight of Levosimendan Impurity 10 is 245.28.

What is the molecular formula of Levosimendan Impurity 10?

The molecular formula of Levosimendan Impurity 10 is C13H15N3O2.

Is Levosimendan Impurity 10 a pure substance?

No, Levosimendan Impurity 10 is an impurity.

What is the significance of Levosimendan Impurity 10 in pharmaceutical manufacturing?

Levosimendan Impurity 10 is important to monitor and control to ensure the purity of the final product.

How is Levosimendan Impurity 10 detected during the manufacturing process?

Levosimendan Impurity 10 can be detected using analytical techniques such as HPLC or LC-MS.

What are the potential risks of having Levosimendan Impurity 10 in the final product?

Having Levosimendan Impurity 10 in the final product can affect the efficacy and safety of the medication.

Can Levosimendan Impurity 10 impact the shelf life of the pharmaceutical product?

Yes, Levosimendan Impurity 10 can potentially reduce the shelf life of the product.

How can pharmaceutical companies prevent the presence of Levosimendan Impurity 10 in their products?

Pharmaceutical companies can implement rigorous quality control and analytical testing procedures to minimize the presence of Levosimendan Impurity 10.

Are there regulatory guidelines that specify the acceptable levels of Levosimendan Impurity 10 in pharmaceutical products?

Yes, regulatory bodies like the FDA and EMA have guidelines on impurities, including Levosimendan Impurity 10, in pharmaceutical products.

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