Dicycloverine EP Impurity A

INQUIRY Add to cart

For Research Use Only | Not For Clinical Use

CAT	APB60263549
CAS	60263-54-9
Structure
Molecular Weight	210.32
Molecular Formula	C13H22O2

What is the specific chemical compound referred to as Dicycloverine EP Impurity A?

Dicycloverine EP Impurity A refers to a specific chemical compound with CAS number 60263-54-9.

What is the molecular weight of Dicycloverine EP Impurity A?

The molecular weight of Dicycloverine EP Impurity A is 210.32 g/mol.

What is the molecular formula of Dicycloverine EP Impurity A?

The molecular formula of Dicycloverine EP Impurity A is C13H22O2.

What is the significance of identifying impurities in pharmaceutical compounds?

Identifying impurities in pharmaceutical compounds is crucial for ensuring the safety, efficacy, and quality of the final product.

How is Dicycloverine EP Impurity A typically synthesized or produced?

Dicycloverine EP Impurity A may be synthesized through various chemical reactions or processes in a laboratory setting.

Why is it important to accurately characterize impurities in pharmaceutical products?

Accurately characterizing impurities in pharmaceutical products is essential for regulatory compliance and ensuring patient safety.

Can impurities in pharmaceutical products potentially impact their stability or shelf life?

Yes, impurities in pharmaceutical products can potentially impact their stability, efficacy, and shelf life.

What analytical techniques are commonly used to identify and quantify impurities in pharmaceutical compounds?

Common analytical techniques used to identify and quantify impurities in pharmaceutical compounds include HPLC, GC-MS, and NMR spectroscopy.

How does the presence of impurities in a pharmaceutical compound affect its overall purity?

The presence of impurities in a pharmaceutical compound reduces its overall purity and can have negative implications for its safety and efficacy.

How can the identification and removal of impurities in pharmaceutical products be achieved?

The identification and removal of impurities in pharmaceutical products can be achieved through rigorous testing, quality control measures, and purification processes.

* Products or Services Interested: Dicycloverine EP Impurity A (60263-54-9)
* Your question
* Name
* Email
Verification Code

Send Us a Request

What is your specific need? We will do everything we can to meet your expectations.

Online Inquiry