Description

Apoatropine CAS NO 500-55-0 is a tropane alkaloid and a key pharmaceutical intermediate derived from atropine. This compound is valued for its specific pharmacological activity and serves as a crucial building block in advanced organic synthesis. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of specialized therapeutics, analytical reference standards, and novel bioactive molecules.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the synthesis of more complex therapeutic agents and active pharmaceutical ingredients (APIs).
• Biochemical Research: Used as a reference standard and tool compound in pharmacological studies, particularly those investigating anticholinergic pathways and receptor binding.
• Analytical Chemistry: Employed as a high-purity standard for method development and quality control in HPLC, LC-MS, and other chromatographic analyses.
• Academic & Industrial R&D: Facilitates exploratory chemistry and the development of new chemical entities in both university and corporate research laboratories.

Basic Information

Product Name	Apoatropine
CAS No.	500-55-0
Molecular Formula	C17H21NO2
Molecular Weight	271.35 g/mol
Synonyms	Apoatropine; Atropamine; DL-Apoatropine; (±)-Apoatropine; NSC 406170; Tropic acid ester with apotropine; 3α-Hydroxy-8-methyl-8-azabicyclo[3.2.1]octane-2β-carboxylic acid tropate
EINECS	207-904-5

Quality Control

Our Apoatropine is produced and tested under a rigorous quality management system. Each batch is analyzed to meet exacting purity standards suitable for research and pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided to ensure full traceability and compliance with your project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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