Description

Antilirium is a high-purity pharmaceutical compound, also known by its systematic chemical name. This compound is a critical active pharmaceutical ingredient (API) and intermediate, valued for its specific pharmacological activity in targeted therapeutic applications. It is essential for manufacturers in the pharmaceutical and advanced life science research sectors requiring reliable, high-quality raw materials for formulation and development.

Application

• Pharmaceutical API: Primary use as an active pharmaceutical ingredient in formulated drug products.
• Neurological Research: Utilized in preclinical and clinical research studies targeting specific neurological pathways.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Chemical Synthesis: Acts as a key intermediate or building block in the synthesis of more complex therapeutic molecules.

Basic Information

Product Name	Antilirium
CAS No.	71214-04-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Antilirium; 71214-04-5; (RS)-2-[(Diethylamino)methyl]-1-phenylcyclopentanol cyclopentyl(2-hydroxyethyl) ether; 1-Phenyl-1-cyclopentyl-2-(diethylamino)ethanol; Cyclopentadrine; Cyclopentamine; Phencyclopentamine
EINECS	Contact for details

Quality Control

Our Antilirium is produced and tested under strict quality management systems to ensure it meets the stringent requirements for pharmaceutical use. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant ICH guidelines and can support compliance with cGMP standards for API manufacturing upon request.

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). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture. For long-term storage, consider the use of desiccants.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
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.