3-Me-PCE

buy high purity 3-MeO-PCE online – Comprehensive Analytical Profile for Laboratory Study

3-MeO-PCE, formally known as 3-Methoxyeticyclidine, is a dissociative research chemical of growing interest in analytical chemistry, forensic toxicology, and structural–activity research. As part of the arylcyclohexylamine family, it is structurally related to ketamine and PCP analogues, making it a valuable compound for laboratory studies, reference standard validation, and comparative analysis.

---

1. Chemical Identity & Classification

3-MeO-PCE belongs to the arylcyclohexylamine dissociative family, which includes ketamine analogues and PCP derivatives.

Chemical Overview

• IUPAC Name: 2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone

• Class: Dissociative research chemical

• Family: Arylcyclohexylamine derivatives

• Common Research Applications: Analytical method development, forensic identification, SAR studies, instrument calibration

The 3-methoxy substitution on the phenyl ring and the ethylamino side chain provide unique analytical fingerprints, which distinguish 3-MeO-PCE from other dissociatives in forensic and laboratory analysis.

---

2. Research Significance of 3-MeO-PCE reference material

3-MeO-PCE has gained attention in the scientific community for its analytical value, especially in the study of novel psychoactive substances (NPS).

Key Research Applications

• Forensic Toxicology: Used to identify and differentiate dissociative analogues in seized samples.

• Instrument Calibration: Provides consistent reference data for GC-MS, LC-MS, and NMR.

• Structure–Activity Relationship (SAR) Studies: Supports research on the effects of minor substitutions on arylcyclohexylamines.

• Metabolic Profiling: Assists in understanding breakdown pathways and potential metabolites.

Its reproducibility and structural clarity make 3-MeO-PCE a reliable analytical reference for laboratories focusing on dissociative research chemicals.

---

3. Characteristics of 3-MeO-PCE analytical standard

3-MeO-PCE is valued for its distinct chromatographic and spectroscopic features, which are essential for accurate laboratory identification.

3.1 Mass Spectrometry (MS)

• EI-MS and ESI-MS: Produces identifiable fragmentation patterns.

• HRMS: Determines precise molecular formulas for unknown or novel analogues.

3.2 Chromatography

• GC-MS: Useful for volatile or thermally stable samples.

• LC-MS/MS: Ideal for polar or labile compounds.

• HPLC: Supports retention-time comparison and analytical method validation.

3.3 NMR & FTIR

• NMR Spectroscopy: Confirms molecular structure and detects positional isomers.

• FTIR: Provides rapid, non-destructive functional group analysis.

These analytical techniques make 3-MeO-PCE a benchmark compound for modern forensic and analytical laboratories.

---

4. Laboratory and Forensic Applications of 3-MeO-PCE reference material

4.1 Forensic Analysis

Forensic laboratories often utilize 3-MeO-PCE to:

• Identify novel dissociatives in casework

• Update early-warning NPS databases

• Provide validated reference spectra for unknown samples

4.2 Method Validation

Analytical chemists incorporate 3-MeO-PCE into instrument validation studies, ensuring:

• Calibration accuracy

• Retention-time consistency

• Fragmentation pattern reproducibility

4.3 Research and SAR Studies

In academic settings, 3-MeO-PCE helps explore:

• Effects of methoxy substitution on receptor binding

• Structural analogues comparison

• Stability and degradation under laboratory conditions

Its inclusion in comparative datasets strengthens data reliability for peer-reviewed studies.

---

5. Purity, Stability, and Handling of dissociative research chemical

Maintaining high-purity 3-MeO-PCE is critical for reproducible results in analytical studies. Impurities can:

• Complicate spectral analysis

• Affect retention times

• Introduce quantification errors

Stability Considerations

• Sensitive to light, heat, and moisture

• Degrades over time if stored improperly

• Requires airtight, light-resistant containers in controlled environments

---

6. Safety and Storage Guidelines

Handling 3-MeO-PCE requires professional laboratory practices.

Recommended Guidelines

• Use gloves, lab coat, and protective eyewear

• Avoid direct contact and inhalation

• Store in a cool, dark, and dry environment

• Follow local regulations and institutional safety protocols

Note: 3-MeO-PCE is for research use only and not intended for human or veterinary consumption.

---

7. Subtle Benefits of Using High-Quality Reference Standards

Using well-documented 3-MeO-PCE from a trusted supplier provides several advantages:

• Reliable Analytical Data: High-purity standards ensure accuracy in MS and NMR analysis.

• Time-Saving: Reduces preparation errors and repeat analyses.

• Enhanced Compliance: Supports labs in meeting regulatory requirements for reference material usage.

• Benchmarking: Helps maintain consistency across multiple laboratories for comparative research.

---

8. Emerging Trends in Dissociative Research (2025)

• AI-Assisted Spectral Analysis: Machine learning predicts fragmentation patterns for new arylcyclohexylamines.

• Portable Detection Tools: On-site GC-MS and FTIR devices allow rapid preliminary analysis.

• Global Early-Warning Networks: Shared datasets enable labs worldwide to respond faster to emerging analogues.

• Metabolomics Integration: Research increasingly examines dissociative metabolism for toxicology studies.

These innovations make 3-MeO-PCE an increasingly valuable component of analytical workflows.

---

9. Conclusion

3-MeO-PCE remains a critical research chemical for laboratories studying dissociative NPS and arylcyclohexylamine analogues. Its distinct structural features, reliable chromatographic and spectroscopic properties, and broad utility in forensic and analytical research make it a trusted reference material.

For researchers looking for precision, reproducibility, and reliable analytical standards, high-quality 3-MeO-PCE ensures consistent results while supporting scientific compliance and integrity.