Description

1-(2-Benzhydryloxy-Ethyl)-Piperazine Dihydrochloride is a high-purity, specialized organic salt primarily used as a key pharmaceutical intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its value lies in its well-defined chemical structure, which is critical for constructing complex molecules with specific biological activity. This compound is essential for research and development chemists and manufacturers in the pharmaceutical and fine chemical industries, particularly those focused on developing new therapeutic agents.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel drug candidates, particularly in central nervous system (CNS) and other therapeutic areas.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in the multi-step production of complex APIs requiring a piperazine-based moiety.
• Chemical Research & Development: Serves as a versatile reagent in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization.
• Fine Chemical Production: Employed in the manufacture of high-value, low-volume specialty chemicals for advanced applications.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control in pharmaceutical laboratories.

Basic Information

Product Name	1-(2-Benzhydryloxy-Ethyl)-Piperazine Dihydrochloride
CAS No.	110407-21-1
Molecular Formula	C19H24N2O·2HCl
Molecular Weight	377.33 g/mol
Synonyms	1-[2-(Diphenylmethoxy)ethyl]piperazine dihydrochloride; 1-(2-(Benzhydryloxy)ethyl)piperazine dihydrochloride; 2-(Benzhydryloxy)ethylpiperazine dihydrochloride; 1-(2-(Diphenylmethoxy)ethyl)piperazine hydrochloride (1:2); Piperazine, 1-[2-[(diphenylmethyl)oxy]ethyl]-, dihydrochloride
EINECS	Contact for details

Quality Control

Our 1-(2-Benzhydryloxy-Ethyl)-Piperazine Dihydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing purity, impurity profile, and physical characteristics is provided with every shipment to support your quality assurance and regulatory compliance needs.

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). This material is hygroscopic (moisture-sensitive) and must be kept under dry conditions to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Water Content (KF)	≤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.