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Lidocaine EP impurity K (free acid)

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For Research Use Only | Not For Clinical Use
CATAPB74634665
CAS74634-66-5
Structure
Molecular Weight220.32
Molecular FormulaC13H20N2O

What is the molecular weight of Lidocaine EP impurity K (free acid)?

The molecular weight of Lidocaine EP impurity K (free acid) is 220.32.

What is the molecular formula of Lidocaine EP impurity K (free acid)?

The molecular formula of Lidocaine EP impurity K (free acid) is C13H20N2O.

Is Lidocaine EP impurity K (free acid) a free acid form?

Yes, Lidocaine EP impurity K is in its free acid form.

What is the CAS number of Lidocaine EP impurity K (free acid)?

The CAS number of Lidocaine EP impurity K (free acid) is 74634-66-5.

What is the chemical structure of Lidocaine EP impurity K (free acid)?

The chemical structure of Lidocaine EP impurity K (free acid) contains carbon, hydrogen, nitrogen, and oxygen atoms.

What is the significance of impurities in pharmaceuticals?

Impurities can impact the efficacy, safety, and stability of pharmaceutical products, so it is important to monitor and control impurity levels.

How can impurities in pharmaceuticals be identified and characterized?

Impurities can be identified and characterized using analytical techniques such as mass spectrometry, chromatography, and spectroscopy.

Why is it important to specify the type of impurity present in a pharmaceutical product?

Different types of impurities may have different effects on the quality and safety of a pharmaceutical product, so it is important to know the specific impurity present.

What are some common sources of impurities in pharmaceutical products?

Impurities can arise from starting materials, intermediates, byproducts, degradation products, and environmental contaminants during the manufacturing process.

How can impurities be controlled or minimized in pharmaceutical manufacturing?

Impurities can be controlled or minimized by optimizing manufacturing processes, using high-quality raw materials, monitoring and testing for impurities at various stages, and implementing good manufacturing practices.

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