Production Semi-Synthétique d'Amoxicilline
Embed This Widget
Add the script tag and a data attribute to embed this widget.
Embed via iframe for maximum compatibility.
<iframe src="https://chemfyi.com/iframe/entity//" width="420" height="400" frameborder="0" style="border:0;border-radius:10px;max-width:100%" loading="lazy"></iframe>Paste this URL in WordPress, Medium, or any oEmbed-compatible platform.
https://chemfyi.com/entity//Add a dynamic SVG badge to your README or docs.
[](https://chemfyi.com/entity//)Use the native HTML custom element.
L'antibiotique le plus prescrit au monde
Aperçu
Amoxicillin is a broad-spectrum semi-synthetic penicillin and the most prescribed antibiotic globally. It is produced by enzymatic coupling of 6-aminopenicillanic acid (6-APA) with D-p-hydroxyphenylglycine (D-HPG) using penicillin G acylase. This enzymatic route has largely replaced chemical acylation methods, providing higher selectivity, milder conditions, and dramatically reduced solvent waste. The process exemplifies the successful integration of biocatalysis in pharmaceutical manufacturing.
Procédé chimique
6-APA is obtained by enzymatic deacylation of penicillin G using immobilized penicillin G acylase. The 6-APA is then coupled with activated D-HPG methyl ester using the same or similar acylase enzyme under controlled pH and temperature to produce amoxicillin trihydrate.
Matières premières
-
6-APA (6-aminopenicillanic acid) — Enzymatic cleavage of penicillin G (Beta-lactam core)
-
D-p-Hydroxyphenylglycine (D-HPG) — Enzymatic resolution or fermentation (Side-chain amino acid)
-
Penicillin G acylase (enzyme) — Recombinant E. coli (Biocatalyst)
Produits finis
-
Amoxicillin trihydrate (C₁₆H₁₉N₃O₅S·3H₂O) — Broad-spectrum antibiotic (Compendial grade)
Environmental Impact
The enzymatic process is significantly greener than chemical acylation, eliminating the need for silylation reagents, organic solvents, and cryogenic conditions. Immobilized enzymes can be reused hundreds of times. Wastewater treatment is simplified due to reduced chemical usage.
Considérations de sécurité
- ⚠ Beta-lactam allergen exposure — dedicated production facilities required
- ⚠ API dust is a potent sensitizer
- ⚠ Enzyme preparations may cause respiratory sensitization
- ⚠ Cold chain required for enzyme storage
Innovations récentes
New engineered acylases with improved thermostability and selectivity are enabling fully aqueous, room-temperature synthesis.
Integration of continuous enzymatic reactors with in-line crystallization is reducing production costs in developing countries.
Échelle de production
21000
tonnes/an
$2.5 billion
valeur marchande
Plus dans Pharmaceutical & Drug Manufacturing
Production de Pénicilline G par Fermentation
Global Industrial Scale
Production d'Insuline Humaine Recombinante
Global Industrial Scale
Synthèse de l'Aspirine par Acétylation de l'Acide Salicylique
Global Industrial Scale
Synthèse de l'Ibuprofène — Procédé Vert BHC
Global Industrial Scale
Synthèse de l'Oméprazole pour les Inhibiteurs de la Pompe à Protons
Global Industrial Scale
Synthèse du Chlorhydrate de Metformine
Global Industrial Scale
Synthèse du Paracétamol (Acétaminophène)
Global Industrial Scale