MilliporeSigma

Small Molecules Analysis & Quality Control (QC)

Small molecules characterization, method development, validation, quality control and quality assurance (QA/QC), safety, purity, potency

Small molecule method development and analysis which includes medicinal chemistry, metabolite identification, impurity profiling, drug metabolism and pharmacokinetics, are key to the success of pharmaceutical quality control and assurance. Successful testing and release of small molecule drugs is dependent on efficient analytical tools, validation guidelines and practices.

There are several methods available for the separation of small molecules and their identification. Some include wet chemistry, high performance liquid chromatography (HPLC), gas chromatography (GC), thin-layer chromatography (TLC), capillary electrophoresis (CE), nuclear magnetic resonance spectroscopy (NMR) and mass spectrometry (MS).

Contact our analytical expert today and get advanced support on method development and workflow tools for accurate and reproducible small molecule analysis.


Related Technical Articles

Related Protocols

Find More Articles and Protocols





Highlights

From development to drug release, this interactive PDF outlines a range of reliable, consistent filters and reagents for dissolution testing protocol
A Quick Guide to Successful Dissolution Testing

From development to drug release, this interactive PDF outlines a range of reliable, consistent filters and reagents for dissolution testing protocol

Download Now
This series of technical articles of the Analytix Reporter special edition outlines biologics characterization being performed in the LC-MS lab.
Analytix Reporter: Pharma Analysis & QC

This serie of technical articles of the Analytix Reporter special edition outlines biologics characterization being performed in the LC-MS lab.

Download Now
This capabilities brochure outlines our extensive pharma analysis & QC portfolio and how our expertise and services can support all workflow steps.
Brochure: Secure your Pharma QC

This capabilities brochure outlines our extensive pharma analysis & QC portfolio and how our expertise and services can support all workflow steps.

Download Now
With over 200 respondents balanced across regions, roles and company types, we believe the results of our survey to be meaningfu
A Practical Guide to HPLC: Develop Your Method with Confidence

Get extensive details on developing and optimizing your HPLC method, including column and mobile phase selection, and troubleshooting common issues.

Download Now
Sign In To Continue

To continue reading please sign in or create an account.

Don't Have An Account?