Tenofovir Impurity 29

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For Research Use Only | Not For Clinical Use

CAT	APB31618903
CAS	31618-90-3
Molecular Weight	322.31
Molecular Formula	C12H19O6PS

What is the product name of CAS 31618-90-3?

The product name is Tenofovir Impurity 29.

What is the molecular weight of Tenofovir Impurity 29?

The molecular weight of Tenofovir Impurity 29 is 322.31.

Can you provide the molecular formula of Tenofovir Impurity 29?

The molecular formula of Tenofovir Impurity 29 is C12H19O6PS.

What is the chemical structure of Tenofovir Impurity 29 based on its molecular formula?

The chemical structure of Tenofovir Impurity 29 contains carbon (C), hydrogen (H), oxygen (O), phosphorus (P), and sulfur (S) atoms arranged in a specific configuration.

What is the significance of identifying impurities such as Tenofovir Impurity 29 in pharmaceutical products?

Identifying impurities such as Tenofovir Impurity 29 is crucial in pharmaceutical products as they can affect the efficacy and safety of the drug, leading to potential adverse effects on patients.

How is Tenofovir Impurity 29 detected and quantified in pharmaceutical formulations?

Tenofovir Impurity 29 can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

What are the possible sources of Tenofovir Impurity 29 in pharmaceutical manufacturing processes?

Tenofovir Impurity 29 can potentially arise from raw materials, intermediates, reaction by-products, degradation processes, or impurities in equipment used during pharmaceutical manufacturing.

How can the presence of Tenofovir Impurity 29 impact the shelf life of pharmaceutical products?

The presence of Tenofovir Impurity 29 can lead to accelerated degradation of the active pharmaceutical ingredient, potentially reducing the shelf life of the product.

What measures can be taken to control and minimize the formation of Tenofovir Impurity 29 during pharmaceutical manufacturing?

Measures such as optimizing reaction conditions, using high-quality raw materials, implementing robust analytical methods for impurity detection, and proper equipment maintenance can help control and minimize the formation of Tenofovir Impurity 29.

How important is the identification and control of impurities like Tenofovir Impurity 29 in ensuring the quality and safety of pharmaceutical products?

The identification and control of impurities such as Tenofovir Impurity 29 are essential for ensuring the quality, safety, and efficacy of pharmaceutical products, as regulatory agencies have strict guidelines for impurity limits in pharmaceutical formulations.

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