Description

Chlorphenoxamine is a versatile organic compound with significant applications in pharmaceutical research and development. This compound is valued for its specific pharmacological activity, making it a key intermediate in the synthesis of active pharmaceutical ingredients (APIs). It is primarily sought after by research institutions and manufacturers in the pharmaceutical and fine chemical industries for developing therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of antihistaminic and anticholinergic active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and development of new therapeutic compounds targeting specific receptors.
• Reference Standard: Serves as a high-purity analytical standard in quality control laboratories for method development and validation.
• Fine Chemical Synthesis: Employed as a specialized intermediate in multi-step organic synthesis for producing complex molecules.

Basic Information

Product Name	Chlorphenoxamine
CAS No.	77-38-3
Molecular Formula	C18H22ClNO
Molecular Weight	303.83 g/mol
Synonyms	2-[1-(4-Chlorophenyl)-1-phenylethoxy]-N,N-dimethylethanamine; Chlorphenoxamine Hydrochloride (salt form); Paryzol; Histachlorphen; Clorevan; Phenoxene; N,N-Dimethyl-2-[(1-phenyl-1-(4-chlorophenyl)ethoxy]ethylamine
EINECS	201-019-1

Quality Control

Our Chlorphenoxamine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets stringent specifications for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all critical quality attributes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0%

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