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Sulfadimidine EP Impurity G-1

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For Research Use Only | Not For Clinical Use
CATAPB1036633358
CAS1036633-35-8
Molecular Weight312.77
Molecular FormulaC12H13ClN4O2S

What is the CAS number for Sulfadimidine EP Impurity G-1?

The CAS number for Sulfadimidine EP Impurity G-1 is 1036633-35-8.

What is the molecular weight of Sulfadimidine EP Impurity G-1?

The molecular weight of Sulfadimidine EP Impurity G-1 is 312.77.

What is the molecular formula of Sulfadimidine EP Impurity G-1?

The molecular formula of Sulfadimidine EP Impurity G-1 is C12H13ClN4O2S.

What is the chemical structure of Sulfadimidine EP Impurity G-1?

The chemical structure of Sulfadimidine EP Impurity G-1 contains carbon, hydrogen, chlorine, nitrogen, oxygen, and sulfur atoms.

How does Sulfadimidine EP Impurity G-1 differ from pure Sulfadimidine?

Sulfadimidine EP Impurity G-1 is an impurity of Sulfadimidine, which means it is a byproduct or a compound present in small quantities along with the main compound.

What potential effects could Sulfadimidine EP Impurity G-1 have in a pharmaceutical product?

Sulfadimidine EP Impurity G-1 could potentially affect the purity and efficacy of a pharmaceutical product if present in high levels.

Is Sulfadimidine EP Impurity G-1 related to any specific health risks?

Sulfadimidine EP Impurity G-1 may pose health risks if present in pharmaceutical products at high levels, due to its impurity status.

How is Sulfadimidine EP Impurity G-1 detected in pharmaceutical samples?

Sulfadimidine EP Impurity G-1 can be detected using analytical techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

What steps can be taken to minimize the presence of Sulfadimidine EP Impurity G-1 in pharmaceutical manufacturing?

Stringent quality control measures and purification processes can be implemented to minimize the presence of Sulfadimidine EP Impurity G-1 in pharmaceutical manufacturing.

Are there any regulations or guidelines regarding the allowable levels of Sulfadimidine EP Impurity G-1 in pharmaceutical products?

Regulatory authorities may have specific limits or guidelines regarding the allowable levels of Sulfadimidine EP Impurity G-1 in pharmaceutical products to ensure safety and efficacy.

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