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JWH 016

Item No. 10849

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(1-butyl-2-methyl-1H-indol-3-yl)-1-naphthalenyl-methanone
CAS Number
155471-09-3
Molecular Formula
C24H23NO
Formula Weight
341.5
Purity
≥95%
Formulation
A 10 mg/ml solution in methanol
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 10 mg/mlEthanol: 10 mg/ml
λmax
218, 320 nm
SMILES
O=C(C1=C(C)N(CCCC)C2=C1C=CC=C2)C3=C(C=CC=C4)C4=CC=C3
InChi Code
InChI=1S/C24H23NO/c1-3-4-16-25-17(2)23(21-13-7-8-15-22(21)25)24(26)20-14-9-11-18-10-5-6-12-19(18)20/h5-15H,3-4,16H2,1-2H3
InChi Key
QKXRHYJSCZFHEK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    5 mg

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    Product Description

    JWH 016 (Item No. 10849) is an analytical reference standard categorized as a synthetic cannabinoid.1,2 JWH 016 induces discriminative stimulus effects in rhesus monkeys comparable to those induced by Δ9-THC (Item Nos. ISO60157 | 12068).3 This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Aung, M.M., Griffin, G., Huffman, J.W., et al. Influence of the N-1 alkyl chain length of cannabimimetic indoles upon CB1 and CB2 receptor binding. Drug Alcohol Depend. 60(2), 133-140 (2000).

    2. Wiley, J.L., Compton, D.R., Dai, D., et al. Structure-activity relationships of indole- and pyrrole-derived cannabinoids. J. Pharmacol. Exp. Ther. 285(3), 995-1004 (1998).

    3. Wiley, J.L., Huffman, J.W., Balster, R.L., et al. Pharmacological specificity of the discriminative stimulus effects of Δ9-tetrahydrocannabinol in rhesus monkeys. Drug Alcohol Depend. 40(1), 81-86 (1995).