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chiral chromatography

Chiral Chromatography: Principles, Methods & Pharma Applications

Two enantiomers of the same molecule share almost every physical property. They boil at the same temperature. They melt at the same point. They dissolve the same way in the same solvent. A standard distillation column cannot tell them apart, and neither can ordinary chromatography. So how does the pharmaceutical industry actually separate one mirror-image

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nitrosamine impurities

Nitrosamine Impurities in APIs: Causes, Risks & FDA Guidelines

In 2018, regulators pulled valsartan tablets off shelves worldwide after finding trace amounts of a chemical called NDMA inside the active ingredient. Ranitidine and metformin followed a similar path over the next two years. The common thread was a class of compounds known as nitrosamines, and the fallout changed how the entire industry looks at

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racemization

What is Racemization in Chemistry? Mechanisms & Pharma Impact

You spend weeks purifying a compound to 99% ee, and if storage conditions are wrong, that single enantiomer slides back toward a 50:50 mixture within days. That process is racemization, the conversion of an optically active compound into a racemic mixture, along with the loss of optical activity. The molecule doesn’t disappear and no bonds

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Optical Isomerism

What is Optical Isomerism? Definition, Examples & Pharma Impact

Two molecules can share the exact same chemical formula and the exact same atom-to-atom connections, yet behave completely differently in the body. The only difference between them is a mirror-image arrangement in 3D space. This is optical isomerism, and it’s one of the more surprising ideas in organic chemistry once you see it in action.

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Solid Phase Peptide Synthesis

A Comprehensive Guide to Solid Phase Peptide Synthesis (SPPS)

Peptide drugs are having a moment. GLP-1 medicines like semaglutide and tirzepatide have turned peptide manufacturing into one of the busiest corners of the pharmaceutical industry. Behind almost all of that production sits one core method: solid phase peptide synthesis, or SPPS. The technique was developed by Robert Bruce Merrifield in the 1960s, work that

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Enantiomeric Excess

Enantiomeric Excess (ee): Definition, Formula, and Pharmaceutical Importance

In chiral chemistry, making a molecule with the right handedness is only half the job. What actually matters is how much of the wrong handed version is mixed in. Enantiomeric excess, usually written as ee, is the number chemists use to describe that purity. It tells you how far a mixture sits from being 50:50

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