Amifostine Impurity 18 (Trihydrobromide)

INQUIRY Add to cart

For Research Use Only | Not For Clinical Use

CAT	APB03288
Synonyms	2,2'-((azanediylbis(propane-3,1-diyl))bis(azanediyl))diethanol trihydrobromide
Molecular Weight	462.05
Molecular Formula	C10H25N3O2·3HBr

What is the molecular weight of Amifostine Impurity 18 (Trihydrobromide)?

The molecular weight of Amifostine Impurity 18 (Trihydrobromide) is 462.05.

What is the molecular formula of Amifostine Impurity 18 (Trihydrobromide)?

The molecular formula of Amifostine Impurity 18 (Trihydrobromide) is C10H25N3O2·3HBr.

What are the synonyms for Amifostine Impurity 18 (Trihydrobromide)?

One of the synonyms is 2,2'-((azanediylbis(propane-3,1-diyl))bis(azanediyl))diethanol trihydrobromide.

How many hydrogen bromide molecules are present in the molecular formula of Amifostine Impurity 18?

There are 3 hydrogen bromide molecules present in the molecular formula of Amifostine Impurity 18.

What is the chemical structure of Amifostine Impurity 18 (Trihydrobromide)?

The chemical structure of Amifostine Impurity 18 (Trihydrobromide) consists of a central nitrogen atom bonded to two propane-diol groups and three hydrogen bromide molecules.

How does Amifostine Impurity 18 differ from the main compound Amifostine?

Amifostine Impurity 18 is a specific impurity of the main compound Amifostine, typically present in small quantities during synthesis or storage.

Is Amifostine Impurity 18 (Trihydrobromide) a commonly encountered impurity in pharmaceutical manufacturing?

The presence of Amifostine Impurity 18 (Trihydrobromide) as an impurity in pharmaceutical manufacturing may vary depending on specific synthesis and purification processes.

What is the significance of identifying impurities like Amifostine Impurity 18 in pharmaceutical products?

Identifying and characterizing impurities like Amifostine Impurity 18 is crucial for ensuring the quality, safety, and efficacy of pharmaceutical products.

How can analytical techniques be used to detect and quantify impurities like Amifostine Impurity 18?

Analytical techniques such as chromatography, spectroscopy, and mass spectrometry can be utilized to detect and quantify impurities like Amifostine Impurity 18.

Are there regulatory guidelines that address the control of impurities in pharmaceutical products, including Amifostine Impurity 18?

Yes, regulatory authorities such as the FDA and EMA have guidelines that specify limits and requirements for the control of impurities in pharmaceutical products, including Amifostine Impurity 18.

* Products or Services Interested: Amifostine Impurity 18 (Trihydrobromide) ()
* 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