Description

Etilefrin Hydrochloride is a synthetic sympathomimetic amine used primarily as a pharmaceutical active ingredient. This compound is critical for its vasoconstrictive and cardiac stimulant properties, making it essential for the development of specific therapeutic formulations. It is primarily required by pharmaceutical manufacturers and research institutions engaged in cardiovascular and hypotensive drug development and synthesis.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of finished dosage forms for cardiovascular medications.
• Active Pharmaceutical Ingredient (API): Direct incorporation into formulations for the treatment of hypotension and orthostatic circulatory disorders.
• Research & Development: Used in pharmacological studies and clinical research for investigating adrenergic receptor activity.
• Reference Standard: Serves as a high-purity analytical standard for quality control testing in pharmaceutical laboratories.
• Veterinary Pharmaceuticals: Potential application in veterinary medicine for circulatory support.

Basic Information

Product Name	Etilefrin Hydrochloride
CAS No.	534-87-2
Molecular Formula	C10H15NO2 • HCl
Molecular Weight	217.69 g/mol
Synonyms	Ethylphenylephrine Hydrochloride; 1-(3-Hydroxyphenyl)-2-ethylaminoethanol Hydrochloride; Etilfenin Hydrochloride; Effortil® (trade name); Etilefrine Hydrochloride; 2-Ethylamino-1-(3-hydroxyphenyl)ethanol Hydrochloride; α-[(Ethylamino)methyl]-3-hydroxybenzyl alcohol hydrochloride
EINECS	208-607-7

Quality Control

Our Etilefrin Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee traceability and compliance.

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). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water (KF Titration)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any individual impurity ≤ 0.5%

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