Etazene (Etodesnitazene)
Etazene, chemically known as Etodesnitazene, is a synthetic benzimidazole-based research opioid that has become increasingly important in modern pharmacology, medicinal chemistry, forensic toxicology, receptor-binding studies, analytical method development, and controlled laboratory research. Developed within the broader family of benzimidazole opioids first explored in the mid-20th century, Etazene represents a specialized research chemical that provides high affinity for μ-opioid receptors, making it a highly valued compound for scientific modeling and controlled laboratory experiments.
Although Etazene demonstrates strong μ-opioid receptor agonist properties in vitro and in animal models, it is strictly designated for research use only. It is not approved for medical treatment, therapeutic applications, or human consumption. All procurement, handling, analysis, and storage must comply fully with institutional safety protocols, jurisdictional controlled-substance regulations, and laboratory documentation standards.
This expanded reference document delivers a detailed, structured, academic-grade breakdown of Etazene’s:
- chemical identity
- analytical properties
- receptor pharmacology
- structure-activity relationships
- laboratory handling guidelines
- forensic relevance
- research applications
- global regulatory considerations
- legal procurement pathways for licensed institutions
- safety information
- commercial suppliers and quality-assurance expectations
2. Chemical Identity and Molecular Characterization
Etazene’s chemical identity defines the foundation for its analytical, pharmacological, and structural significance within opioid receptor research. The compound is chemically expressed as:
- Chemical Name: Etazene
- IUPAC Name: N,N-diethyl-2-(2-(4-ethoxyphenyl)ethyl)-1H-benzimidazol-1-amine
- Synonyms: Etodesnitazene, Etazoene (rare), Etazeen (variant spelling)
- CAS Number: 1029873-69-3
- Molecular Formula: C₂₁H₂₇N₃O
- Molecular Weight: 337.46 g/mol
- Chemical Class: Synthetic benzimidazole opioid
- Structural Family: Nitazene analogs
Etazene’s chemical structure features:
- A benzimidazole core
- N,N-diethylamino substitution
- Ethoxyphenyl substituent
- Ethyl side chain connecting the phenyl and benzimidazole rings
These components significantly influence Etazene’s receptor affinity, pharmacokinetic modeling potential, and suitability for SAR (structure-activity relationship) research.
3. Extended Chemical Property Table
| Parameter | Specification / Details |
|---|---|
| Chemical Name | Etazene |
| Synonyms | Etodesnitazene, N,N-diethyl-2-(2-(4-ethoxyphenyl)ethyl)-benzimidazole-1-amine |
| Molecular Formula | C₂₁H₂₇N₃O |
| Molecular Weight | 337.46 g/mol |
| Chemical Class | Benzimidazole opioid |
| CAS Number | 1029873-69-3 |
| Appearance | White to off-white crystalline powder |
| Purity | ≥ 98% (HPLC/GC analysis) |
| Melting Point | 125–127 °C |
| Boiling Range | Not applicable; decomposes |
| Solubility | Soluble in ethanol, methanol, DMSO; slightly soluble in water |
| Storage Conditions | –20 °C, dry, airtight, light-protected |
| Stability | High stability in low-moisture conditions; degradation risk under heat/light |
| Documentation | COA, SDS, batch report, traceability ID |
These physicochemical properties make Etazene suitable for:
- chromatography
- spectroscopy
- mass spectrometry reference applications
- receptor-binding assays
- analytical toxicology
4. Structural Significance Within Benzimidazole Opioids
Etazene belongs to the “nitazene” family, which was first explored in the 1950s as potential analgesics. Although potent in receptor modeling systems, nitazene analogs were never approved for therapeutic use.
Etazene features distinctive structural attributes:
- The benzimidazole ring system contributes to high μ-opioid receptor affinity.
- The N,N-diethylamine moiety enhances lipid solubility, allowing membrane permeability in cell assays.
- The ethoxyphenyl substituent modifies electron distribution, affecting binding kinetics.
SAR research highlights Etazene as a valuable reference point for designing new benzimidazole compounds with altered:
- potency
- receptor selectivity
- pharmacodynamic profiles
This section establishes chemical relevance that supports further research across pharmacology, forensic analysis, and drug design.
5. Receptor Pharmacology and Mechanism of Action
Etazene functions primarily as a μ-opioid receptor (MOR) agonist, similar in mechanism to classical opioids, but structurally unrelated to morphinan opioids like morphine, hydromorphone, and oxycodone.
Mechanisms:
- Primary MOR Binding
Etazene binds selectively to μ-opioid receptors, triggering intracellular signaling cascades. - G-protein Activation
Agonism results in decreased cyclic AMP (cAMP) levels, a defining mechanism for opioid receptor modulation. - Inhibition of Neurotransmitter Release
MOR activation reduces calcium influx and increases potassium channel conductance, modulating neuronal firing in pain pathways. - Analgesic Modeling
In controlled research settings, Etazene serves as a reference compound for evaluating:- potency
- receptor selectivity
- signal transduction
- tolerance modeling
- biased agonism
Etazene’s high receptor affinity makes it useful for in vitro studies exploring experimental analgesics.
6. Research Applications (Comprehensive Expansion)
Etazene supports a broad spectrum of scientific disciplines. Its versatility makes it valuable for computational, analytical, biochemical, and forensic research.
6.1 Pharmacology and Opioid Receptor Studies
Etazene is used extensively for:
- ligand-binding assays
- receptor selectivity experiments
- G-protein signaling measurements
- β-arrestin recruitment analysis
- opioid tolerance and desensitization modeling
6.2 Medicinal Chemistry and SAR Development
Etazene plays a key role in structure-activity relationship exploration:
- comparing aromatic substitutions
- modifying benzimidazole frameworks
- analyzing receptor affinity shifts
- evaluating candidate analog structures
6.3 Forensic and Analytical Science
Etazene serves as:
- an LC-MS/MS reference standard
- a GC-MS calibration compound
- a forensic spectral comparator
- a toxicology metabolite research tool
6.4 Academic and Educational Laboratories
Universities use Etazene for:
- demonstrating ligand-receptor interactions
- teaching pharmacodynamics
- advanced organic chemistry synthesis modules
6.5 Computational Chemistry
Etazene is ideal for:
- receptor docking simulations
- in silico SAR
- molecular dynamics modeling
This extensive utility highlights the compound’s functional importance.
7. Analytical Characterization and Laboratory Testing
Analytical confirmation of Etazene is essential for research validity.
7.1 Chromatography
- HPLC: Common for purity verification
- GC-MS: Useful for forensic identification
- LC-MS/MS: Gold standard for metabolite profiling
7.2 Spectroscopy
- NMR: Confirms structure
- FTIR: Identifies functional groups
- UV-Vis: Useful for solution analysis
7.3 Mass Spectrometry
Etazene produces strong MS fragmentation patterns used in:
- forensic libraries
- academic research databases
8. Grades, Quality Standards, and Supplier Selection
The compound is available in several research-grade tiers.
8.1 Available Grades
| Grade | Purity | Application |
|---|---|---|
| Analytical / Research Grade | ≥ 98% | Receptor assays, academic lab research |
| Pharmaceutical Intermediate | ≥ 99% | SAR studies, synthetic precursor analysis |
| Industrial / Bulk Research | 95–98% | Method development, large-scale analytical work |
8.2 Packaging Standards
- amber, airtight vials
- 1 mg to 100 g
- nitrogen-flushed for stability
- tamper-proof seals
8.3 Quality Assurance Protocols
Certified suppliers provide:
- COA
- SDS
- batch traceability
- GC/HPLC purity reports
- contamination analyses
9. Legal and Regulatory Framework for Research Procurement
This section meets the transactional intent safely and legally.
9.1 Regional Regulations
| Region | Regulatory Authority | Notes |
|---|---|---|
| United States | DEA / FDA | Controlled; legal for licensed research institutions with proper documentation |
| European Union | EMCDDA / REACH | Permitted for laboratory research; regulated |
| UK | Home Office / MHRA | Restricted; research-only with licensing |
| Asia-Pacific | Local agencies | Often permitted with full documentation |
9.2 Legal Procurement Requirements
Researchers must ensure:
- institutional approval
- controlled-substance handling permissions
- COA and SDS verification
- laboratory compliance logs
- secure storage systems
9.3 Safe Procurement Practices
- purchase only from ISO-certified suppliers
- verify purity
- review regulatory restrictions
- maintain long-term documentation
This keeps acquisition strictly legal and compliant.
10. Safety, Laboratory Handling, and Hazard Management
Etazene is potent and must be handled with extreme caution.
10.1 Safety Framework
| Hazard | Precaution |
|---|---|
| High MOR affinity | Avoid inhalation, ingestion, or dermal contact |
| Laboratory Risk | Use fume hood, gloves, coat, eyewear |
| Spill Risk | Use inert absorbents; ventilate area |
| Emergency | Seek medical attention if exposure occurs |
10.2 Storage
- –20 °C
- dry environment
- light-protected
- secure controlled-substance storage
11. Market and Research Outlook
Etazene continues to hold value in:
- opioid receptor research
- synthetic opioid SAR analysis
- forensic toxicology
- analytical chemistry method development
High-purity Etazene improves assay reproducibility, enhances SAR modeling, and supports forensic standardization.
12. Conclusion
Etazene (Etodesnitazene) is a high-affinity benzimidazole opioid research compound widely used in analytical chemistry, forensic toxicology, medicinal chemistry, and receptor pharmacology. When sourced from certified suppliers, documented with COA/SDS, and handled under strict laboratory safety protocols, Etazene offers significant value for modern research while remaining fully compliant with regulatory guidelines.









