DeschcloroKetamine (DCK) Pellets – 20mg

A. Introduction

Deschloroketamine (DCK) Pellets 20mg are premium laboratory-grade research pellets containing arylcyclohexylamine dissociative analog lacking chlorine substitution, designed for scientific institutions and analytical laboratories investigating NMDA receptor ligands. This high-purity compressed pellet format provides researchers with consistent 20mg units for method validation, structural analysis, and reference comparisons in controlled settings.

B. Scientific Overview

DCK belongs to the arylcyclohexylamine class structurally related to ketamine but featuring 2-oxo-ethylamino substitution on phenylcyclohexyl 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 244), and spectroscopic signatures of dechlorinated dissociative anesthetics.

Laboratory investigations focus on its chemical properties including solubility profiles (10-15 mg/mL DMSO/methanol), thermal stability, and quantitative recovery characteristics under LC-MS/MS conditions, without reference to biological interactions.

C. Product Specifications

• Form: Compressed pellets containing 20mg deschloroketamine HCl per unit for precise lab handling

• Label per unit: 20mg analytical portions (resealable packaging)

• Synonym: 2′-Oxo-PCM, DXE, DCK

• CAS Number: 4631-27-0

• Molecular Formula: C₁₅H₂₁NO- HCl

• Molecular Weight: 267.80 g/mol

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

• Storage Conditions: Cool, dry place (2-8°C recommended), protected from light/moisture for stability

D. Laboratory Use Context

Deschloroketamine (DCK) Pellets 20mg are 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 them in controlled environments for quantitative analysis at ng/mL concentrations, positive ionization studies, and stability testing via HPLC/UV protocols. The standardized 20mg pellet format ensures reproducible mass transfer and quantitative recovery in analytical workflows.

E. Quality & Testing

Every batch receives comprehensive quality control:

• Certificate of Analysis (COA) with HPLC, MS, NMR identity confirmation and pellet uniformity testing

• Full batch traceability from synthesis through compression and verification

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

• Manufactured under controlled conditions ensuring consistent pellet weight (±2%) and dissolution performance

F. Shipping & Handling

Discreet worldwide shipping to verified research laboratories via secure, compliant carriers. Packaging meets IATA/DOT standards for research chemicals, with protective containment 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.