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Tryptophan EP Impurity G

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For Research Use Only | Not For Clinical Use
CATAPB21704803
CAS21704-80-3
Molecular Weight220.23
Molecular FormulaC11H12N2O3

What is the product name of CAS 21704-80-3?

The product name is Tryptophan EP Impurity G.

What is the molecular weight of Tryptophan EP Impurity G?

The molecular weight is 220.23.

What is the molecular formula of Tryptophan EP Impurity G?

The molecular formula is C11H12N2O3.

Can you explain what is an EP Impurity in relation to Tryptophan?

EP Impurity refers to impurities in Tryptophan that are considered within acceptable limits according to the European Pharmacopoeia standards.

What is the significance of CAS 21704-80-3 in relation to Tryptophan EP Impurity G?

CAS 21704-80-3 is the unique identification number assigned to Tryptophan EP Impurity G for reference and tracking purposes.

How does the molecular weight of Tryptophan EP Impurity G impact its properties?

The molecular weight of Tryptophan EP Impurity G affects its solubility, stability, and reactivity in various chemical processes.

What are the potential uses of Tryptophan EP Impurity G in pharmaceutical or research applications?

Tryptophan EP Impurity G may be used as a reference standard, intermediate, or in research studies related to Tryptophan and its impurities.

How is Tryptophan EP Impurity G typically synthesized or obtained?

Tryptophan EP Impurity G can be synthesized through chemical reactions or isolated from specific sources through extraction and purification processes.

Are there any specific safety precautions or guidelines to be followed while handling Tryptophan EP Impurity G?

It is recommended to follow proper lab safety protocols, use appropriate protective equipment, and handle Tryptophan EP Impurity G in a controlled environment to avoid potential hazards.

How does the presence of Impurity G affect the overall quality or purity of Tryptophan in pharmaceutical products?

The presence of Impurity G in Tryptophan may impact the efficacy, stability, and regulatory compliance of pharmaceutical products, which highlights the importance of monitoring and controlling impurities in drug manufacturing processes.

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