Description

Bencyclane is a synthetic organic compound with significant pharmacological activity, primarily functioning as a vasodilator. This makes it a critical intermediate in the synthesis of active pharmaceutical ingredients (APIs) for treating cerebrovascular and peripheral circulatory disorders. It is essential for pharmaceutical manufacturers and R&D facilities focused on developing and producing cardiovascular and nootropic medications.

Application

• Pharmaceutical Intermediate: Primary use as a key building block in the synthesis of the vasodilator drug Bencyclane Fumarate.
• API Production: Serves as a direct precursor in the manufacturing of the final Active Pharmaceutical Ingredient for medicinal formulations.
• Research & Development: Used in pharmacological studies and the development of new therapeutic agents targeting vascular and cerebral functions.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Chemical Synthesis: Utilized in organic synthesis for creating novel compounds with potential spasmolytic and vasoactive properties.

Basic Information

Item	Detail
Product Name	Bencyclane
CAS No.	2179-37-5
Molecular Formula	C19H27NO2
Molecular Weight	301.43 g/mol
Synonyms	3-(1-Benzylcycloheptyl)oxy-1-methylpropylamine; Bencyclan; Bencyclane base; Fludilat; Halidor; Ludilat; 1-[(1-Benzylcycloheptyl)oxy]-3-(methylamino)propane; NSC 113986
EINECS	218-546-9

Quality Control

Our Bencyclane is produced under strict quality management systems to ensure high purity and batch-to-batch consistency. Quality is verified through a comprehensive suite of analytical tests including HPLC, GC, and NMR. A Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each shipment. We support compliance with cGMP, ICH Q7 guidelines, and relevant pharmacopoeial standards for pharmaceutical intermediates.

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 the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 10 ppm

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