Description

Piperidolate Hydrochloride is a pharmaceutical-grade active pharmaceutical ingredient (API) and chemical intermediate of significant commercial importance. Its primary value lies in its anticholinergic and antispasmodic properties, making it a critical component for research and development in therapeutic applications. This compound is essential for pharmaceutical manufacturers, research institutions, and chemical synthesis laboratories focused on developing treatments for gastrointestinal disorders and other related conditions.

Application

• Pharmaceutical API: Primary use as an active ingredient in the formulation of antispasmodic and anticholinergic medications.
• Chemical Intermediate: Serves as a key building block in the synthesis of more complex pharmaceutical compounds and fine chemicals.
• Biomedical Research: Utilized in pharmacological studies to investigate muscarinic receptor antagonism and smooth muscle physiology.
• Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
• Preclinical Development: Used in the early-stage development of new therapeutic agents targeting gastrointestinal motility.

Basic Information

Product Name	Piperidolate Hydrochloride
CAS No.	129-77-1
Molecular Formula	C21H25NO2·HCl
Molecular Weight	359.89 g/mol
Synonyms	Piperidolate HCl; 1-Ethyl-3-piperidyl diphenylacetate hydrochloride; Dactil; Piptal; JB-305; Diphenylacetic acid 1-ethyl-3-piperidinyl ester hydrochloride; NSC 73913
EINECS	204-950-9

Quality Control

Our Piperidolate Hydrochloride is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and conformance to agreed specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled under appropriate conditions to prevent degradation.

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%
Loss on Drying	≤1.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Individual impurity ≤0.5%; Total impurities ≤1.5%

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