Levosimendan Impurity 13

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For Research Use Only | Not For Clinical Use

What is the product name of CAS 103416-88-2?

The product name is Levosimendan Impurity 13.

What is the molecular weight of Levosimendan Impurity 13?

The molecular weight is 204.23.

What is the molecular formula of Levosimendan Impurity 13?

The molecular formula is C11H12N2O2.

How is Levosimendan Impurity 13 categorized?

It is categorized as an impurity of Levosimendan.

What is the significance of understanding Levosimendan Impurity 13 in pharmaceutical research?

Understanding Levosimendan Impurity 13 is important for ensuring the purity and efficacy of Levosimendan in pharmaceutical formulations.

How can Levosimendan Impurity 13 be detected and quantified in pharmaceutical samples?

It can be detected and quantified through analytical techniques such as HPLC or LC-MS.

What are the potential implications of the presence of Levosimendan Impurity 13 in pharmaceutical products?

The presence of impurities like Levosimendan Impurity 13 can impact the quality, safety, and efficacy of pharmaceutical products.

How is Levosimendan Impurity 13 synthesized or produced?

Levosimendan Impurity 13 may be synthesized through specific chemical reactions or processes during the manufacturing of Levosimendan.

What precautions should be taken to minimize the formation of impurities like Levosimendan Impurity 13 in pharmaceutical production?

Strict quality control measures, proper storage conditions, and adherence to good manufacturing practices can help minimize impurity formation.

Are there any regulatory guidelines or limits regarding the presence of Levosimendan Impurity 13 in pharmaceutical products?

Regulatory bodies may set specific limits or guidelines for impurities in pharmaceutical products, which may include Levosimendan Impurity 13.

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