Description

Tribenoside is a synthetic glycoside compound with established pharmacological properties, primarily recognized for its venotonic and anti-inflammatory effects. This high-purity active pharmaceutical ingredient (API) is essential for formulators requiring reliable and consistent raw material quality for therapeutic applications. It is specifically targeted at the pharmaceutical and advanced research sectors for the development of topical and systemic treatments for vascular disorders.

Application

• Pharmaceutical API: Primary use as the active ingredient in prescription and over-the-counter (OTC) medications for venous insufficiency, hemorrhoids, and related vascular conditions.
• Topical Formulations: Incorporated into creams, ointments, and gels designed to reduce inflammation, edema, and discomfort associated with venous stasis.
• Oral Dosage Forms: Used in the production of tablets and capsules for systemic treatment of chronic venous diseases.
• Veterinary Pharmaceuticals: Applied in medicinal products for treating similar vascular conditions in animals.
• Biomedical Research: Serves as a reference standard and key compound in pharmacological studies focusing on vascular permeability and inflammation pathways.
• Cosmeceutical Preparations: Found in specialized cosmetic products aimed at reducing the appearance of dark circles and puffiness related to microcirculation issues.

Basic Information

Product Name	Tribenoside
CAS No.	10310-32-4
Molecular Formula	C₂₉H₃₈O₁₀
Molecular Weight	546.61 g/mol
Synonyms	Glyvenol; Tribenosidum; 3,5,6-Tri-O-benzyl-D-glucofuranose; 1,2-O-(1-Methylethylidene)-3,5,6-tri-O-phenylmethyl-α-D-glucofuranose; D-Glucofuranose, 1,2-O-(1-methylethylidene)-3,5,6-tris-O-(phenylmethyl)-; Tribenozide; Tribenosid; 1,2-O-Isopropylidene-3,5,6-tri-O-benzyl-α-D-glucofuranose
EINECS	233-689-7

Quality Control

Our Tribenoside is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) detailing purity, related substances, and residual solvents are provided with every shipment to support your regulatory and formulation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after each use to prevent moisture absorption, which may affect stability and performance.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.