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Methyl salicylate EP impurity E

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For Research Use Only | Not For Clinical Use
CATAPB5985240
CAS5985-24-0
Structure
Molecular Weight210.19
Molecular FormulaC10H10O5

What is the full name of the chemical compound with CAS 5985-24-0?

The full name of the chemical compound with CAS 5985-24-0 is Methyl salicylate EP impurity E.

What is the molecular weight of Methyl salicylate EP impurity E?

The molecular weight of Methyl salicylate EP impurity E is 210.19.

What is the molecular formula of Methyl salicylate EP impurity E?

The molecular formula of Methyl salicylate EP impurity E is C10H10O5.

What is the chemical structure of Methyl salicylate EP impurity E?

The chemical structure of Methyl salicylate EP impurity E is made up of 10 carbon atoms, 10 hydrogen atoms, and 5 oxygen atoms bonded together in a specific arrangement.

How is Methyl salicylate EP impurity E used in pharmaceutical manufacturing?

Methyl salicylate EP impurity E is used as an impurity reference standard in pharmaceutical manufacturing to ensure product quality and consistency.

What is the significance of EP in the name Methyl salicylate EP impurity E?

The EP in the name indicates that Methyl salicylate EP impurity E meets the standards set by the European Pharmacopoeia.

Can Methyl salicylate EP impurity E be used as an active ingredient in pharmaceutical products?

No, Methyl salicylate EP impurity E is not used as an active ingredient in pharmaceutical products but as an impurity reference standard.

How is Methyl salicylate EP impurity E synthesized in the laboratory?

Methyl salicylate EP impurity E can be synthesized in the laboratory through specific chemical reactions involving the appropriate precursors.

What role does Methyl salicylate EP impurity E play in quality control processes of pharmaceutical products?

Methyl salicylate EP impurity E serves as a benchmark in quality control processes to ensure that pharmaceutical products meet regulatory standards for impurity levels.

What are the potential risks associated with the presence of Methyl salicylate EP impurity E in pharmaceutical products?

The presence of Methyl salicylate EP impurity E in pharmaceutical products can lead to potential quality control issues, regulatory non-compliance, and potential adverse effects on patient safety.

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