Description

Ecabet Sodium is a synthetic diterpenoid derivative with potent gastroprotective and anti-ulcer properties. This compound is valued for its unique mechanism of action, which involves strengthening the gastric mucosal barrier and inhibiting the activity of *Helicobacter pylori*. It is primarily utilized in the pharmaceutical industry for the formulation of prescription medications targeting peptic ulcers and gastritis.

Application

• Pharmaceutical Active Ingredient (API): Core component in prescription drugs for the treatment and prevention of gastric and duodenal ulcers.
• Gastroprotective Formulations: Used in combination therapies to enhance mucosal defense mechanisms against acid and pepsin.
• Anti-*H. pylori* Agents: Incorporated into therapeutic regimens aimed at eradicating *Helicobacter pylori* infections.
• Clinical Research: Serves as a reference standard and key material in pharmacological studies and drug development pipelines.
• Veterinary Pharmaceuticals: Applied in formulations for treating gastrointestinal disorders in animals.

Basic Information

Product Name	Ecabet Sodium
CAS No.	86408-72-2
Molecular Formula	C20H27NaO5S
Molecular Weight	402.48 g/mol
Synonyms	Ecabet Sodium; Sodium Ecabet; (+)-(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-6-sulfo-1-phenanthrenecarboxylic Acid Sodium Salt; TA-2711; Gastrom; GU-ECABET; UNII-8K713B34Y5
EINECS	Contact for details

Quality Control

Our Ecabet Sodium is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC, to ensure it meets high-purity pharmaceutical standards. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry conditions to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm

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