HXE Powder

A. Introduction

HXE Powder is a premium laboratory-grade research chemical containing hydroxetamine, an arylcyclohexylamine dissociative analog structurally related to O-desmethyl methoxetamine (MXE), designed for scientific institutions and analytical laboratories investigating NMDA receptor ligands. This high-purity powder provides researchers with consistent material for method validation, structural analysis, and reference comparisons in controlled settings.

B. Scientific Overview

HXE belongs to the arylcyclohexylamine class characterized by its 3-hydroxyphenyl-cyclohexanone-ethylamine scaffold suitable for analytical profiling. In research contexts, it functions as an analytical reference for studying chromatographic behavior, mass spectrometry fragmentation patterns ([M+H]+ m/z 234.1489), and spectroscopic signatures of hydroxylated dissociative structures.

Laboratory investigations focus on its chemical properties including solubility profiles (20 mg/mL DMF, 10 mg/mL DMSO), thermal stability, and quantitative recovery characteristics under LC-MS/MS conditions, without reference to biological interactions.

C. Product Specifications

• Form: White to off-white fine crystalline powder for precise lab handling

• Label per unit: 1g analytical portions (resealable, inert packaging)

• Synonym: Hydroxetamine, 3-HO-2′-Oxo-PCE, O-Desmethyl MXE

• CAS Number: 1620054-73-0

• Molecular Formula: C₁₄H₁₉NO₂

• Molecular Weight: 233.31 g/mol

• Purity: ≥98% (HPLC, typical batch purity)

• Storage Conditions: -20°C freezer, desiccated, protected from light/moisture for stability

D. Laboratory Use Context

HXE Powder is designated solely for in-vitro analytical research, including reference standard preparation, LC-MS/MS method optimization for arylcyclohexylamines, forensic profiling of dissociative metabolites, and impurity detection in complex matrices.

Researchers apply it in controlled environments for quantitative analysis at ng/mL concentrations, positive ionization studies, and stability testing via HPLC/UV protocols. The fine powder form ensures reproducible mass transfer critical for LOQ/LOD determination in forensic workflows.

E. Quality & Testing

Every batch receives comprehensive quality control:

• Certificate of Analysis (COA) with HPLC, LC-HRMS, NMR identity confirmation

• Full batch traceability from synthesis through recrystallization and verification

• Third-party laboratory testing for purity, homogeneity, and residual solvents

• Manufactured under controlled conditions ensuring consistent crystal morphology and analytical performance

F. Shipping & Handling

Discreet worldwide shipping to verified research laboratories via secure, compliant carriers. Packaging meets IATA/DOT standards for research chemicals, with thermal protection and full documentation for customs clearance. Tracking provided; buyers confirm jurisdictional import compliance prior to purchase.

G. Compliance Disclaimer

For Research Use Only. Not for human consumption.
This product is supplied strictly as a laboratory reagent for analytical purposes. It is not approved for human, veterinary, diagnostic, or therapeutic applications. No statements imply biological effects beyond in-vitro research contexts.

Qualified researchers and institutions assume full responsibility under local, federal, and international laws. Seller disclaims all liability for non-research use. Consult safety data sheets and institutional protocols before handling.