Description

Hydroxyamphetamine is a synthetic organic compound belonging to the class of phenethylamines. This chemical is valued for its role as a key intermediate and reference standard in advanced pharmaceutical research and analytical chemistry. It is primarily utilized by research institutions, pharmaceutical development laboratories, and quality control facilities. The compound's specific structure makes it relevant for studies in neuroscience and metabolic pathways.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of more complex active pharmaceutical ingredients (APIs) and diagnostic agents.
• Analytical Reference Standard: Used as a high-purity calibrant in chromatographic methods (HPLC, GC) for quantitative and qualitative analysis in forensic, clinical, and pharmaceutical testing.
• Biochemical Research: Employed in neuroscience and pharmacological studies to investigate adrenergic and dopaminergic receptor interactions and metabolic processes.
• Metabolite Standard: Essential for the identification and quantification of amphetamine-related metabolites in toxicology and doping control laboratories.
• Process Development: Used in scaling up and optimizing synthetic routes within R&D and pilot-scale chemical production.

Basic Information

Product Name	Hydroxyamphetamine
CAS No.	1518-86-1
Molecular Formula	C9H13NO
Molecular Weight	151.21 g/mol
Synonyms	4-Hydroxyamphetamine; p-Hydroxyamphetamine; Oxilofrine; 1-(4-Hydroxyphenyl)-2-aminopropane; 4-HA; Norfenefrine Impurity; Para-hydroxyamphetamine; α-Methyl-4-hydroxybenzeneethanamine
EINECS	Contact for details

Quality Control

Our Hydroxyamphetamine is produced and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, detailing results from tests such as HPLC assay, related substances, residual solvents, and identification. Our quality commitment aligns with cGMP principles 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 (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider inert atmosphere conditions to ensure stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 1.0%

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