Sotalol hydrochloride EP impurity B HCl

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For Research Use Only | Not For Clinical Use

What is the product name of this impurity?

The product name is Sotalol hydrochloride EP impurity B HCl.

What is the CAS number of this impurity?

The CAS number is 5576-49-8.

What is the molecular weight of Sotalol hydrochloride EP impurity B HCl?

The molecular weight is 306.81.

What is the molecular formula of this impurity?

The molecular formula is C12H19ClN2O3S.

Is Sotalol hydrochloride EP impurity B HCl a salt or a hydrochloride?

It is a hydrochloride, as indicated by the "HCl" in its name.

What elements are present in the molecular formula of this impurity?

The molecular formula includes carbon (C), hydrogen (H), chlorine (Cl), nitrogen (N), oxygen (O), and sulfur (S).

Why is it important to know the impurity profile of a pharmaceutical product?

Understanding the impurity profile is crucial for ensuring the quality, safety, and efficacy of the product.

How can impurities like Sotalol hydrochloride EP impurity B HCl affect the stability of a drug?

Impurities can degrade the active ingredient, alter its pharmacological properties, or lead to toxic effects.

What methods are typically used to detect and quantify impurities in pharmaceuticals?

Analytical techniques such as HPLC, GC-MS, and NMR spectroscopy are commonly used for impurity analysis.

How can the presence of impurities be minimized during the manufacturing process?

Stringent quality control measures, proper storage conditions, and purification steps can help minimize impurities in pharmaceutical products.

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