Description

Trimebutine Maleate is a high-purity pharmaceutical active ingredient, a maleate salt form of the antispasmodic agent trimebutine. This compound is critical for ensuring the quality and efficacy of finished pharmaceutical products targeting gastrointestinal motility disorders. It is primarily required by manufacturers in the pharmaceutical industry for the production of prescription medications.

Application

• Active Pharmaceutical Ingredient (API) in the formulation of prescription drugs for the treatment of irritable bowel syndrome (IBS).
• Key Intermediate in advanced pharmaceutical synthesis and research for gastrointestinal therapeutics.
• Reference Standard for quality control and analytical method development in pharmaceutical laboratories.
• Clinical Research Material for studies investigating treatments for functional gastrointestinal disorders.
• Formulation Development for creating various dosage forms such as tablets and capsules.

Basic Information

Product Name	Trimebutine Maleate
CAS No.	345659-09-8
Molecular Formula	C22H31NO5 • C4H4O4
Molecular Weight	503.56 g/mol
Synonyms	Trimebutine hydrogen maleate; 2-(Dimethylamino)-2-phenylbutyl 3,4,5-trimethoxybenzoate maleate; 3,4,5-Trimethoxybenzoic acid 2-(dimethylamino)-2-phenylbutyl ester maleate; Debridat (as maleate salt); Polibutin (as maleate salt); Trimedat; Modulon
EINECS	Contact for details

Quality Control

Our Trimebutine Maleate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are provided with every shipment.

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). Due to its hygroscopic nature, protect from moisture and store under inert conditions if the container is opened frequently.

Specification

Item	Specification
Appearance	White to off-white crystalline 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)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0%; Any single impurity ≤ 0.5%

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