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Methylphenidate EP Impurity C

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For Research Use Only | Not For Clinical Use
CATAPB50288625
CAS50288-62-5
Molecular Weight218.3
Molecular FormulaC13H18N2O

What is the CAS number for Methylphenidate EP Impurity C?

The CAS number for Methylphenidate EP Impurity C is 50288-62-5.

What is the molecular weight of Methylphenidate EP Impurity C?

The molecular weight of Methylphenidate EP Impurity C is 218.3.

What is the molecular formula of Methylphenidate EP Impurity C?

The molecular formula of Methylphenidate EP Impurity C is C13H18N2O.

What is the structure of Methylphenidate EP Impurity C based on its molecular formula?

The structure of Methylphenidate EP Impurity C based on its molecular formula contains 13 carbon atoms, 18 hydrogen atoms, 2 nitrogen atoms, and 1 oxygen atom.

How does Methylphenidate EP Impurity C differ from the active ingredient Methylphenidate?

Methylphenidate EP Impurity C is an impurity of Methylphenidate and is not the active ingredient itself.

What role does Methylphenidate EP Impurity C play in formulations containing Methylphenidate?

Methylphenidate EP Impurity C can affect the purity and quality of formulations containing Methylphenidate.

Is Methylphenidate EP Impurity C considered safe for human consumption?

As an impurity, Methylphenidate EP Impurity C may not be safe for human consumption and should be minimized in drug formulations.

How can the presence of Methylphenidate EP Impurity C be detected in pharmaceutical products?

Analytical techniques such as HPLC (high-performance liquid chromatography) can be used to detect and quantify Methylphenidate EP Impurity C in pharmaceutical products.

Can the levels of Methylphenidate EP Impurity C in pharmaceutical products be regulated?

Regulatory agencies may set limits on the acceptable levels of Methylphenidate EP Impurity C in pharmaceutical products to ensure safety and efficacy.

What are the potential risks associated with high levels of Methylphenidate EP Impurity C in drug formulations?

High levels of Methylphenidate EP Impurity C in drug formulations may lead to impurities, decreased effectiveness, or potential adverse effects on patients.

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