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Carbazochrome Sodium Sulfonate Impurity 25

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For Research Use Only | Not For Clinical Use
CATAPB10344
Molecular Weight382.36
Molecular FormulaC10H14N4O8S2

What is the molecular weight of Carbazochrome Sodium Sulfonate Impurity 25?

The molecular weight of Carbazochrome Sodium Sulfonate Impurity 25 is 382.36.

What is the molecular formula of Carbazochrome Sodium Sulfonate Impurity 25?

The molecular formula of Carbazochrome Sodium Sulfonate Impurity 25 is C10H14N4O8S2.

What is the chemical structure of Carbazochrome Sodium Sulfonate Impurity 25?

The chemical structure of Carbazochrome Sodium Sulfonate Impurity 25 is composed of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms.

What is the significance of Carbazochrome Sodium Sulfonate Impurity 25?

Carbazochrome Sodium Sulfonate Impurity 25 is an impurity that may be found in pharmaceutical products and needs to be monitored and controlled.

What are the potential effects of Carbazochrome Sodium Sulfonate Impurity 25 in pharmaceutical products?

Carbazochrome Sodium Sulfonate Impurity 25 may affect the purity and efficacy of the pharmaceutical product containing it.

How is Carbazochrome Sodium Sulfonate Impurity 25 detected in pharmaceutical products?

Carbazochrome Sodium Sulfonate Impurity 25 can be detected through analytical techniques such as HPLC (High-Performance Liquid Chromatography) and spectroscopy.

What steps can be taken to control the presence of Carbazochrome Sodium Sulfonate Impurity 25?

Manufacturers can implement strict quality control measures during the production process to minimize the presence of Carbazochrome Sodium Sulfonate Impurity 25.

How can the amount of Carbazochrome Sodium Sulfonate Impurity 25 be quantified in a pharmaceutical product?

The amount of Carbazochrome Sodium Sulfonate Impurity 25 can be quantified by comparing its peak area in chromatographic analysis to that of a standard reference.

What is the regulatory requirement regarding Carbazochrome Sodium Sulfonate Impurity 25 in pharmaceutical products?

Regulatory agencies may set limits on the allowable amount of Carbazochrome Sodium Sulfonate Impurity 25 in pharmaceutical products to ensure safety and efficacy.

How can the presence of Carbazochrome Sodium Sulfonate Impurity 25 impact the shelf life of a pharmaceutical product?

The presence of Carbazochrome Sodium Sulfonate Impurity 25 can lead to degradation and reduced shelf life of a pharmaceutical product.

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