Description

Dicycloverine is a synthetic anticholinergic agent, primarily recognized for its antispasmodic properties on smooth muscle. This compound is a critical active pharmaceutical ingredient (API) valued for its ability to provide targeted relief from gastrointestinal spasms and associated pain. It is essential for manufacturers in the pharmaceutical industry, particularly those developing and producing antispasmodic and antiulcer medications. Our high-purity Dicycloverine ensures reliable performance and consistency in final drug formulations.

Application

• Primary Active Pharmaceutical Ingredient (API) in antispasmodic medications.
• Key component in formulations for treating irritable bowel syndrome (IBS) and related gastrointestinal disorders.
• Used in the synthesis of combination drugs for peptic ulcer disease and gastrointestinal hypermotility.
• Intermediate in advanced pharmaceutical research and development of new anticholinergic therapies.
• Reference standard in analytical laboratories for quality control and method validation.

Basic Information

Product Name	Dicycloverine
CAS No.	77-19-0
Molecular Formula	C19H35NO2
Molecular Weight	309.49 g/mol
Synonyms	Dicyclomine; Dicycloverine Hydrochloride; Bentyl; Procyclomin; 2-(Diethylamino)ethyl 1-cyclohexylcyclohexanecarboxylate; 1-Cyclohexylcyclohexanecarboxylic Acid 2-(Diethylamino)ethyl Ester; Merbentyl
EINECS	201-005-8

Quality Control

Our Dicycloverine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, aligning with pharmacopeial 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, well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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