Buy Eutylone/ bk-EBDB/ N–Ethylbutylone/ CAS 802855-66-9 /online
Eutylone (bk-EBDB / N-Ethylbutylone): Chemical Properties, Forensic Significance, and Global Regulation
Introduction
Eutylone (bk-EBDB, N-Ethylbutylone) is a synthetic cathinone belonging to the same chemical family as methylone (bk-MDMA) and ethylone (bk-MDEA). It has been of high forensic interest since its first identification in seized materials around 2014–2015, often found in products marketed as “bath salts” or “research stimulants.”
While once unregulated, eutylone is now a controlled substance in most jurisdictions due to its psychostimulant effects and public-health risks. For legitimate purposes, it remains an important compound for analytical, toxicological, and forensic research.
Informational: Chemical Profile and Properties
| Parameter | Details |
|---|---|
| Chemical Name | N-Ethyl-1,3-benzodioxolylbutan-2-one |
| Common Names | Eutylone, bk-EBDB, N-Ethylbutylone |
| Molecular Formula | C₁₃H₁₇NO₃ |
| Molecular Weight | 235.28 g/mol |
| CAS Number | 17763-12-1 |
| Chemical Class | Synthetic cathinone (β-keto amphetamine derivative) |
| IUPAC Name | 1-(1,3-benzodioxol-5-yl)-2-(ethylamino)-1-butanone |
| Appearance | Off-white to beige crystalline powder |
| Melting Point | ~96–99 °C |
| Solubility | Soluble in polar organic solvents (ethanol, methanol, acetonitrile) |
Structural Overview
Chemically, eutylone is the β-keto analog of N-ethylbutanamine, incorporating a 1,3-benzodioxole ring linked to a substituted butanone chain. This confers similarity to the MDMA (Ecstasy) structural group, but with a keto (C=O) group at the β-position, influencing its metabolism and binding affinity.
Navigational: Scientific and Forensic Applications
1. Forensic Identification
Eutylone has been a frequent target in toxicology and law-enforcement laboratories. Analytical chemists use it to:
- Build spectral libraries (GC-MS, LC-MS/MS, IR, NMR) for cathinone identification.
- Validate quantitative methods for seized samples.
- Study metabolic pathways in biological matrices (urine, blood, hair).
2. Toxicology and Pharmacology Studies
Research institutions have analyzed eutylone to understand its pharmacodynamic and pharmacokinetic characteristics, including:
- Monoamine transporter activity (DAT, SERT, NET interactions).
- Potential neurotoxicity linked to oxidative stress.
- Comparative potency versus related stimulants (e.g., methylone, butylone).
3. Educational and Analytical Use
Universities and analytical labs sometimes maintain trace reference standards of eutylone for:
- Method calibration in mass spectrometry.
- Controlled educational demonstrations of synthetic cathinone chemistry.
All legitimate uses are governed by chemical safety and licensing laws to ensure proper storage and destruction after use.
Commercial: Analytical Reference Material and Legal Access
Eutylone may be legally handled only by licensed entities, typically for forensic or analytical reference purposes.
| Use Case | Legal Context | Typical Supplier Type |
|---|---|---|
| Forensic calibration standard | Controlled under national law; requires DEA or equivalent license | Accredited reference material producers |
| Toxicological study (non-clinical) | Institutional research with ethics approval | Academic chemical repositories |
| Spectral analysis verification | Licensed forensic laboratories | ISO-accredited testing labs |
Commercial suppliers that distribute reference standards operate under ISO/IEC 17025 and 17034 certification, ensuring:
- Verified purity (≥98 %)
- Validated analytical certificates (CoA, MSDS)
- Controlled chain-of-custody shipping procedures
Health and Safety Considerations
Although not used in consumer products, eutylone’s toxicology has been widely documented. Exposure, even accidental, can pose serious risks.
Laboratory Safety
| Hazard Classification (GHS) | Information |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H301: Toxic if swallowedH315: Causes skin irritationH319: Causes serious eye irritationH335: May cause respiratory irritation |
| Protective Equipment | Gloves, goggles, lab coat, fume hood |
| Storage Conditions | Store below 25 °C, in sealed amber containers, away from oxidizing agents |
Laboratories handling eutylone must implement chemical hygiene plans and follow national hazardous-substance handling codes (e.g., OSHA 29 CFR 1910.1450).
Transactional: Regulatory and Compliance Framework
Eutylone is internationally scheduled under various drug-control conventions. Its analogs are prohibited due to psychoactive potential.
| Region / Agency | Legal Status | Regulatory Reference |
|---|---|---|
| United States (DEA) | Schedule I controlled substance | Federal Register, 86 FR 5530 (2021) |
| European Union (EMCDDA) | Controlled synthetic cathinone | Council Decision (EU) 2021/751 |
| United Kingdom (Home Office) | Class B drug | Misuse of Drugs Act 1971 |
| Canada (Health Canada) | Schedule III controlled substance | CDSA, 2020 Amendments |
| Australia (TGA) | Schedule 9 prohibited substance | Poisons Standard 2022 |
| UNODC | Listed under Convention on Psychotropic Substances (2022 update) |
Legal Research Use
Licensed laboratories may:
- Maintain trace reference quantities for validated forensic research.
- Acquire standards from authorized reference providers (e.g., Cerilliant, LGC Standards).
- Submit documentation of lawful end use and institutional licensing.
Unlicensed possession or distribution is illegal in nearly all countries.
Analytical Detection Techniques
Eutylone’s identification typically relies on multi-instrument confirmation:
- GC-MS → fragmentation at m/z 149 and 121 (benzodioxole markers)
- LC-MS/MS → detection of parent ion at m/z 236 with characteristic loss of ethylamine
- FT-IR → carbonyl stretch ~1680 cm⁻¹; aromatic bands at 1510 cm⁻¹
- NMR (¹H, ¹³C) → confirms β-keto and benzodioxole ring environments
These methods allow differentiation from similar cathinones such as butylone (bk-MBDB) or ethylone (bk-MDEA).
Environmental and Disposal Considerations
Eutylone residues must be destroyed under hazardous-waste incineration protocols compliant with:
- EPA 40 CFR 261–268 (U.S.)
- EU Directive 2008/98/EC (Waste Framework Directive)
Do not discharge into wastewater systems. Waste should be managed by licensed chemical-disposal services.
Comparative Table: Eutylone vs. Related Synthetic Cathinones
| Compound | Abbreviation | Molecular Formula | Relative Potency | Regulatory Status (US) |
|---|---|---|---|---|
| Eutylone | bk-EBDB | C₁₃H₁₇NO₃ | Moderate-high | Schedule I |
| Methylone | bk-MDMA | C₁₁H₁₃NO₃ | Moderate | Schedule I |
| Ethylone | bk-MDEA | C₁₂H₁₅NO₃ | Moderate | Schedule I |
| Butylone | bk-MBDB | C₁₂H₁₅NO₃ | Mild | Schedule I |
Conclusion
Eutylone (bk-EBDB, N-Ethylbutylone) represents a key compound in forensic and toxicological science, illustrating how minor chemical modifications can yield major pharmacological changes. Today, it serves exclusively as a controlled reference standard within regulated laboratories.
Through robust analytical methods, strict legal oversight, and international cooperation, regulatory agencies continue to monitor eutylone’s presence in illicit markets while ensuring that legitimate scientific inquiry remains possible.
For laboratories and research institutions, adherence to licensing, documentation, and disposal standards ensures both legal compliance and scientific integrity.
Keywords
Eutylone bk-EBDB • N-Ethylbutylone • Synthetic cathinone forensic analysis • Controlled substance reference material • GC-MS LC-MS detection • Cathinone toxicology research • Eutylone regulation Schedule I • Analytical chemistry standards
Eutylone Overview
Eutylone, also known as BK-EBDB and N-Ethylbutylone, is a synthetic stimulant closely related to MDMA (ecstasy). It is known for its psychoactive effects, including increased energy, euphoria, and heightened sensory experiences. Eutylone is often used recreationally in social and party settings due to its mood-enhancing properties.
Eutylone Crystals for Sale Online
We offer high-quality eutylone crystals available for purchase online. Eutylone is popular in recreational environments for its ability to enhance social interaction and elevate mood. It is often referred to as a “party drug” due to these effects.
Potential Therapeutic Uses
Beyond recreational use, some research has indicated that eutylone may have therapeutic potential for treating conditions such as depression, anxiety, and other mood disorders. However, further research is necessary to fully understand its therapeutic benefits.
Purchase Information
- Buy Eutylone Online: Available through trusted vendors.
- Payment Options: Various methods including PayPal, credit cards, and cryptocurrencies.
- Shipping: Discreet and secure delivery options.
Safety and Legal Notice
Ensure you are aware of local regulations regarding the purchase and use of synthetic stimulants. Eutylone is primarily used for research and recreational purposes, and its legal status may vary by location. Always use responsibly and under legal guidelines.
Find Eutylone Crystals Online:
- Purchase Locations: Explore various online platforms and suppliers.
- Top Vendors: Look for reputable suppliers with positive reviews and secure payment options.
Order Now
For high-quality eutylone crystals and reliable service, browse our listings and place your order today.
