Description

Glycopyrronium Tosylate is a high-purity pharmaceutical intermediate and active ingredient salt. It is a critical compound valued for its anticholinergic properties, which are essential in the development of specific therapeutic formulations. This product is primarily required by manufacturers in the pharmaceutical and advanced fine chemical sectors for research, development, and production.

Application

• Pharmaceutical Active Ingredient (API): Core component in the formulation of anticholinergic medications.
• Research & Development: Key intermediate for synthesizing novel drug candidates targeting muscarinic receptors.
• Production of Finished Dosage Forms: Used in the manufacture of tablets, injectables, or topical preparations requiring glycopyrronium activity.
• Reference Standard: Serves as a high-purity standard for analytical testing and quality control in laboratories.
• Chemical Synthesis: Building block for further chemical modifications and derivative synthesis in advanced organic chemistry.

Basic Information

Product Name	Glycopyrronium Tosylate
CAS No.	1624259-25-1
Molecular Formula	C26H37NO7S
Molecular Weight	507.64 g/mol
Synonyms	Glycopyrrolate Tosylate; Glycopyrronium p-Toluenesulfonate; 3-[(Cyclopentylhydroxyphenylacetyl)oxy]-1,1-dimethylpyrrolidinium Tosylate; Glycopyrrolate Tosylate Salt; 1-Methyl-3-pyrrolidyl α-cyclopentylmandelate p-Toluenesulfonate; Glycopyrronium Tosylate Monohydrate (common form); Glycopyrrolonium Tosylate
EINECS	Contact for details

Quality Control

Our Glycopyrronium Tosylate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) with detailed batch-specific results are provided to guarantee traceability and compliance with relevant industry standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and purity.

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%
Water Content (KF)	≤5.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Individual impurity ≤0.5%; Total impurities ≤2.0%

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