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Pentoxifylline EP Impurity D

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For Research Use Only | Not For Clinical Use
CATAPB59413148
CAS59413-14-8
Molecular Weight238.25
Molecular FormulaC10H14N4O3

What is the CAS number for Pentoxifylline EP Impurity D?

The CAS number for Pentoxifylline EP Impurity D is 59413-14-8.

What is the molecular weight of Pentoxifylline EP Impurity D?

The molecular weight of Pentoxifylline EP Impurity D is 238.25.

What is the molecular formula for Pentoxifylline EP Impurity D?

The molecular formula for Pentoxifylline EP Impurity D is C10H14N4O3.

How does Pentoxifylline EP Impurity D differ from pure Pentoxifylline?

Pentoxifylline EP Impurity D is an impurity of Pentoxifylline, meaning it is a substance that is present in Pentoxifylline which is not the desired pure form of the drug.

How can the presence of Pentoxifylline EP Impurity D affect the quality of Pentoxifylline?

The presence of impurities like Pentoxifylline EP Impurity D in Pentoxifylline can affect the efficacy and safety of the drug, as impurities can alter the pharmacological properties of the active ingredient.

Are impurities like Pentoxifylline EP Impurity D commonly found in pharmaceutical products?

Yes, impurities in pharmaceutical products are common, and regulatory authorities have strict guidelines regarding the acceptable levels of impurities in drugs.

How is the identification and control of impurities like Pentoxifylline EP Impurity D important in the pharmaceutical industry?

The identification and control of impurities are important in ensuring the quality, safety, and efficacy of pharmaceutical products, as impurities can impact the overall functionality of the drug.

What analytical methods can be used to detect and quantify impurities like Pentoxifylline EP Impurity D in pharmaceutical products?

Analytical methods like HPLC (High-Performance Liquid Chromatography) can be used to detect and quantify impurities in pharmaceutical products with high sensitivity and specificity.

How can the presence of Pentoxifylline EP Impurity D be minimized during the manufacturing process of Pentoxifylline?

To minimize the presence of impurities like Pentoxifylline EP Impurity D, strict quality control measures and good manufacturing practices can be implemented to ensure the purity of the final drug product.

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