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Trimebutinil maleate EP impurity C (trimethoprim EP impurity H)

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For Research Use Only | Not For Clinical Use
CATAPB1916070
CAS1916-07-0
Structure
Molecular Weight226.23
Molecular FormulaC11H14O5

What is the molecular weight of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H)?

The molecular weight of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H) is 226.23.

What is the molecular formula of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H)?

The molecular formula of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H) is C11H14O5.

What is the CAS number of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H)?

The CAS number of Trimebutinil maleate EP impurity C (trimethoprim EP impurity H) is 1916-07-0.

How is Trimebutinil maleate EP impurity C related to trimethoprim EP impurity H?

Trimebutinil maleate EP impurity C is also known as trimethoprim EP impurity H.

What class of compound does Trimebutinil maleate EP impurity C belong to?

Trimebutinil maleate EP impurity C belongs to the class of impurities.

What is the significance of identifying impurity C in Trimebutinil maleate?

Identifying impurity C in Trimebutinil maleate is important for quality control and regulatory purposes.

How can impurity C affect the purity of Trimebutinil maleate?

Impurity C can impact the overall purity of Trimebutinil maleate and potentially affect its efficacy and safety.

Are there specific guidelines for the acceptable levels of impurity C in Trimebutinil maleate?

Yes, regulatory agencies often have guidelines for the maximum allowable levels of impurities in pharmaceutical products.

How can impurity levels in pharmaceuticals be determined?

Impurity levels in pharmaceuticals can be determined through various analytical techniques such as HPLC or GC.

What steps can be taken to reduce impurity levels in pharmaceutical manufacturing?

To reduce impurity levels in pharmaceutical manufacturing, strict quality control measures, purification processes, and adherence to good manufacturing practices can be implemented.

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