Ursodeoxycholic Acid (UDCA)

Ursodeoxycholic Acid (UDCA)

Nombre del producto Ursodeoxycholic Acid (UDCA)
Número CAS 128-13-2
Otros nombres 3α,7β-Dihydroxy-5β-cholan-24-oic acid; Ursodiol; Actigall; Urso; Ursofalk
Fórmula molecular C24H40O4
Peso molecular 392.57 g/mol
Apariencia Polvo cristalino de color blanco a blanquecino
Ensayo (HPLC) ≥99,01 TP3T
Punto de fusión 200-204°C
Specific Rotation [α]D20 +58° to +62° (c=2, ethanol)
Pérdida por secado ≤0,51 TP3T
Residuo tras la combustión ≤0,11 TP3T
Metales pesados ≤10 ppm
Solubilidad Sparingly soluble in ethanol, practically insoluble in water
Paquete 25 kg fiber drum with double polyethylene liner

Ursodeoxycholic Acid (UDCA) Structure

Sinónimos: 3α,7β-Dihydroxy-5β-cholan-24-oic acid, Ursodiol, Actigall, Urso, Ursofalk, UDCA

Ursodeoxycholic acid (UDCA) has steadily climbed the ranks of essential bile acid ingredients, driven by its well-documented therapeutic profile and expanding applications in both pharmaceutical and nutraceutical sectors. As the global demand for liver-support formulations and gallstone management therapies rises, UDCA stands out for its dual role as an active pharmaceutical ingredient (API) and a functional excipient in drug delivery systems. Its unique hydrophilic character among bile acids makes it a preferred choice for formulators seeking efficacy and tolerability.

UDCA is a secondary bile acid originally isolated from bear bile, but today it is predominantly produced through multi-step chemical synthesis from cholic acid or chenodeoxycholic acid. This synthetic route ensures consistent supply, high purity, and freedom from animal-derived contaminants, aligning with modern regulatory expectations for pharmaceutical-grade materials. The compound occurs naturally in small quantities in human bile, where it helps maintain cholesterol homeostasis and protects hepatocytes from toxic bile acid accumulation.

Commercially available UDCA is standardized to ≥99.0% purity (HPLC), with strict control over related substances, residual solvents, and heavy metals. Its crystalline form offers excellent stability and flow properties, making it suitable for direct compression, wet granulation, and encapsulation. For B2B buyers, the key selling points are reliable large-scale supply, full regulatory documentation, and a proven track record in approved drug products worldwide.

Descripción general y composición del producto

Chemically, UDCA is a dihydroxy bile acid with a 5β-cholane skeleton, featuring hydroxyl groups at the 3α and 7β positions. This epimerization at C-7 distinguishes it from chenodeoxycholic acid (CDCA) and deoxycholic acid (DCA), conferring greater hydrophilicity and reduced cytotoxicity. The molecule’s amphiphilic nature allows it to interact with cell membranes and modulate signaling pathways without disrupting membrane integrity at therapeutic doses.

In pharmaceutical formulations, UDCA is often used as the active ingredient in tablets and capsules for hepatobiliary disorders. It also serves as a key starting material for the synthesis of other bile acid derivatives, such as tauroursodeoxycholic acid (TUDCA) and glycoursodeoxycholic acid (GUDCA), which are gaining traction in research and supplement markets. Its compatibility with common excipients and ability to form stable salts further broaden its utility.

Aplicaciones principales

  • Pharmaceutical APIs: Primary treatment for primary biliary cholangitis (PBC) and gallstone dissolution; also used in cholestatic liver diseases.
  • Nutraceuticals: Incorporated into liver health and detox supplements, often combined with milk thistle or artichoke extracts.
  • Research & Development: Reference standard for analytical method development and bile acid metabolism studies.
  • Drug Delivery: Enhances bioavailability of poorly soluble drugs through bile acid transport mechanisms.
  • Cosmeceuticals: Emerging use in anti-aging and skin barrier repair formulations due to its cytoprotective properties.

Calidad y normas

Parámetro Especificaciones
Ensayo (HPLC) ≥99,01 TP3T
Pérdida por secado ≤0,51 TP3T
Metales pesados ≤10 ppm
Residuo tras la combustión ≤0,11 TP3T
Límites microbianos Total aerobic count ≤1000 CFU/g; Yeast & Mold ≤100 CFU/g; E. coli absent
Disolventes residuales Meets ICH Q3C requirements

Embalaje y suministros

  • Embalaje: 25 kg fiber drum with double polyethylene liner, or as per customer request.
  • Cantidad mínima de pedido: 1 kg for trial orders; 25 kg for commercial orders.
  • Plazo de entrega: 3-5 días laborables (artículos en stock)
  • Documentación: COA, MSDS, TDS, stability data, and regulatory support available upon request.

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