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Metaraminol bitartrate Impurity G

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For Research Use Only | Not For Clinical Use
CATAPB08698
Molecular Weight299.28
Molecular FormulaC13H17NO7

What is the molecular weight of Metaraminol bitartrate Impurity G?

The molecular weight of Metaraminol bitartrate Impurity G is 299.28.

What is the molecular formula of Metaraminol bitartrate Impurity G?

The molecular formula of Metaraminol bitartrate Impurity G is C13H17NO7.

What is the name of the impurity referred to as Metaraminol bitartrate Impurity G?

The impurity referred to as Metaraminol bitartrate Impurity G.

How many carbon atoms are present in the molecular formula of Metaraminol bitartrate Impurity G?

There are 13 carbon atoms present in the molecular formula of Metaraminol bitartrate Impurity G.

What is the total number of atoms in the molecular formula of Metaraminol bitartrate Impurity G?

The total number of atoms in the molecular formula of Metaraminol bitartrate Impurity G is 37.

Are there any nitrogen atoms present in the molecular formula of Metaraminol bitartrate Impurity G?

Yes, there is one nitrogen atom present in the molecular formula of Metaraminol bitartrate Impurity G.

What is the significance of identifying impurities like Metaraminol bitartrate Impurity G in pharmaceutical products?

Identifying impurities like Metaraminol bitartrate Impurity G is important for ensuring the safety and efficacy of pharmaceutical products.

How is Metaraminol bitartrate Impurity G detected and quantified in pharmaceutical formulations?

Metaraminol bitartrate Impurity G can be detected and quantified using analytical techniques such as HPLC or GC.

What are the potential sources of Metaraminol bitartrate Impurity G in pharmaceutical manufacturing processes?

Metaraminol bitartrate Impurity G can be introduced as a byproduct of synthesis or as a degradation product during storage or handling.

How can the presence of Metaraminol bitartrate Impurity G impact the stability and shelf-life of pharmaceutical products?

The presence of Metaraminol bitartrate Impurity G can impact the stability and shelf-life of pharmaceutical products by affecting their potency, purity, and overall quality.

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