Manufacturing fenbendazole is a multi-step chemical synthesis, not a fermentation or natural extraction.
Here’s the simplified version:
Start with the benzimidazole
This is created by combining o-phenylenediamine with certain carboxylic acids under heat to form the basic benzimidazole ring.
Add the carbamate side chain
This step creates fenbendazole’s ability to dissolve in fats and move through the digestive tract effectively.
Attach a phenylthio (sulfur-linked) group
This thioether group increases potency by helping the compound bind to its target in parasites.
Purify, crystallize, and mill
The final compound is filtered, crystallized, and turned into the fine powder used in animal medications.
This synthesis is performed under pharma-grade conditions in regulated facilities.
It’s not made through fermentation, mold, herbs, or anything biological it’s a fully synthetic lab-based compound.