0

Aztreonam Amination Impurity 1

INQUIRY Add to cart
For Research Use Only | Not For Clinical Use
CATAPB06715
Molecular Weight434.44
Molecular FormulaC13H18N6O7S2

What is the molecular weight of Aztreonam Amination Impurity 1?

The molecular weight of Aztreonam Amination Impurity 1 is 434.44.

What is the molecular formula of Aztreonam Amination Impurity 1?

The molecular formula of Aztreonam Amination Impurity 1 is C13H18N6O7S2.

What is the significance of the term "Amination Impurity 1" in the product name?

The term "Amination Impurity 1" indicates that this is a specific impurity related to amination in the Aztreonam compound.

How does the molecular weight of Aztreonam Amination Impurity 1 impact its chemical properties?

The molecular weight of Aztreonam Amination Impurity 1 can impact its solubility, stability, and interactions with other compounds.

What are the atoms present in the molecular formula of Aztreonam Amination Impurity 1?

The molecular formula of Aztreonam Amination Impurity 1 contains carbon, hydrogen, nitrogen, oxygen, and sulfur atoms.

How does the presence of sulfur in the molecular formula affect the properties of Aztreonam Amination Impurity 1?

The presence of sulfur can contribute to the chemical reactivity and potential for forming different types of bonds in Aztreonam Amination Impurity 1.

Is Aztreonam Amination Impurity 1 considered a pure substance or a mixture?

Aztreonam Amination Impurity 1 is considered an impurity, which means it is a substance present in a compound or mixture that is not the desired product.

What is the role of impurities like Aztreonam Amination Impurity 1 in pharmaceutical manufacturing?

Understanding and controlling impurities like Aztreonam Amination Impurity 1 is important for ensuring the quality, safety, and efficacy of pharmaceutical products.

Are there specific analytical techniques used to detect and quantify Aztreonam Amination Impurity 1?

Yes, analytical techniques such as chromatography and spectroscopy are commonly used to identify and quantify impurities in pharmaceutical compounds.

How can the presence of Aztreonam Amination Impurity 1 impact the regulatory approval of a pharmaceutical product?

The presence of impurities like Aztreonam Amination Impurity 1 must be carefully monitored and controlled to meet regulatory requirements for pharmaceutical purity and safety.

  • Verification code
Contact Us

Send Us a Request

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

Online Inquiry

For any inquiry, question or recommendation, please call: or fill out the following form.

  • Verification code

Head Office

  • Tel:
  • Email:

Follow us on

qrcode