Buy JWH-122 Online – Premium Research Chemical for Sale

JWH – 122 for sale Looking to purchase JWH-122 for research purposes? We offer top-quality JWH-122 with verified lab-grade purity (≥98%) suitable for scientific, analytical, and forensic research. JWH-122 is a potent synthetic cannabinoid that acts primarily as a full agonist at the CB1 and CB2 receptors, making it valuable in the study of endocannabinoid system functions and synthetic cannabinoid pharmacology.

🔬 Product Details:

• Chemical Name: (4-Methyl-1-naphthalenyl)(1-pentyl-1H-indol-3-yl)-methanone

• Molecular Formula: C25H27NO

• Molecular Weight: 357.49 g/mol

• Purity: ≥98% (Lab Verified)

• Form: Off-white to white crystalline powder

• Solubility: Soluble in organic solvents like ethanol and DMSO

• Storage: Store in a cool, dry place away from light

🧪 Key Uses of JWH-122:

• CB1/CB2 receptor binding assays

• Toxicology and forensic analysis

• Metabolite profiling and analytical reference standard

• SAR (Structure-Activity Relationship) studies in synthetic cannabinoids

✅ Why Choose Us?

• ISO-certified labs and verified test results

• Fast, discreet worldwide shipping (where legally permitted)

• Bulk order discounts available

• Secure checkout and professional customer support

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🧪 JWH-122: Uses, Properties, and Manufacturing Process

✅ Chemical Overview

• Chemical Name: (4-Methyl-1-naphthalenyl)(1-pentyl-1H-indol-3-yl)-methanone

• Common Name: JWH-122

• Molecular Formula: C25H27NO

• Molecular Weight: 357.49 g/mol

• CAS Number: 619294-47-2

• Class: Synthetic Cannabinoid (Arylalkylindole family)

⚗️ Properties of JWH-122

🔍 Uses of JWH-122⚠️

1. Pharmacological Research

• Used in the study of CB1 and CB2 receptor binding and activation.

• Helps determine the structure-activity relationship (SAR) among synthetic cannabinoids.

2. Forensic Science & Toxicology

• Employed as a reference standard for identifying unknown substances in seized materials.

• Used in the development of drug screening assays (e.g., LC-MS/MS, GC-MS).

3. Analytical Chemistry

• Used in the calibration and testing of lab equipment.

• Provides a benchmark compound for evaluating metabolites and isomers.

4. Academic & Industrial Research

• Contributes to research in neuropharmacology, behavioral science, and substance interaction studies.

⚙️ Manufacturing Process of JWH-122 (General Overview)⚠️ 

🔬 General Synthetic Route:

JWH-122 is part of the naphthoylindole class of cannabinoids. The process involves combining a naphthoyl chloride with a substituted indole via Friedel–Crafts-type acylation or amide bond formation.

🔧 Step-by-Step Summary

1. Synthesis of Naphthoyl Chloride Intermediate

   • Begin with 4-methyl-1-naphthoic acid.

   • React it with thionyl chloride (SOCl₂) or oxalyl chloride to convert the acid to 4-methyl-1-naphthoyl chloride.

2. Preparation of Substituted Indole

   • Use 1-pentylindole as the indole component, which is often synthesized separately by alkylating indole with 1-bromopentane.

3. Coupling Reaction

   • The naphthoyl chloride is reacted with the 1-pentylindole in the presence of a base (like triethylamine or pyridine) and a solvent (such as dichloromethane or THF).

   • This forms the target compound JWH-122 via nucleophilic acyl substitution.

4. Purification

   • The crude product is purified using column chromatography, recrystallization, or vacuum distillation, depending on purity goals.

5. Characterization

   • Final product is characterized and verified using:

     • NMR (¹H and ¹³C)

     • Mass spectrometry (MS)

     • Infrared spectroscopy (IR)

     • High-performance liquid chromatography (HPLC) for purity

🌍 Legal Status (Overview)

• JWH-122 is classified as a controlled substance in many countries, including:

  • United States: Schedule I (DEA)

  • United Kingdom: Class B substance

  • Germany: Covered under NpSG (New Psychoactive Substances Act)

  • Canada: Schedule II

• Always check local regulations before handling or purchasing this compound.

⚠️ Important Disclaimer

JWH-122 is sold exclusively for laboratory research and forensic use. It is not approved for human consumption, medical use, or veterinary application. Handling requires appropriate PPE and should occur in a certified research environment.

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