Description

Penthienate is a synthetic organic compound belonging to the class of anticholinergic agents. This compound is valued for its specific pharmacological activity, making it a critical intermediate in the research and development of therapeutic drugs. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on neurology and gastroenterology.

Application

• Pharmaceutical Intermediate: Key starting material or intermediate in the synthesis of anticholinergic and antispasmodic medications.
• Research & Development: Used in preclinical and clinical research to study muscarinic receptor antagonists and their effects.
• Active Pharmaceutical Ingredient (API) Synthesis: Employed in the manufacturing process of final drug substances targeting gastrointestinal and urinary tract disorders.
• Biochemical Research: Serves as a tool compound in pharmacological assays and studies of the autonomic nervous system.
• Reference Standard: Used as a certified reference material (CRM) in analytical laboratories for quality control and method validation.

Basic Information

Product Name	Penthienate
CAS No.	22064-27-3
Molecular Formula	C21H29NO3S
Molecular Weight	375.53 g/mol
Synonyms	Penthienate Bromide; (3-Hydroxy-1-methylpiperidin-1-ium-1-yl) 2-cyclopentyl-2-thiophen-2-ylacetate bromide; 2-Cyclopentyl-2-(2-thienyl)acetic Acid 3-Hydroxy-1-methylpiperidinium Bromide Ester; Monodral Bromide; Penthienatum; Poldine (as methosulfate); Thiphenamil; Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our Penthienate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via techniques such as HPLC, IR, and NMR to ensure it meets high-grade standards suitable for pharmaceutical research. A Certificate of Analysis (COA) detailing all test results is 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). Keep away from incompatible materials.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
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.