An Analytical Reference Standard
Features
  • This product has been formulated as an exempt preparation which meets criteria established by the US DEA
  • Possession of a DEA Controlled Substance registration is not necessary nor is a DEA 222 form required to purchase this product
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing
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JWH 398 (exempt preparation)

Item No. 15686

Exempt Product (US)
Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(4-chloro-1-naphthalenyl)(1-pentyl-1H-indol-3-yl)-methanone
CAS Number
1292765-18-4
Molecular Formula
C24H22ClNO
Formula Weight
375.9
Purity
≥95%
Formulation
A 1 mg/mL solution in methanol
λmax
218, 316 nm
SMILES
ClC1=CC=C(C(C2=CN(CCCCC)C3=C2C=CC=C3)=O)C4=C1C=CC=C4
InChi Code
InChI=1S/C24H22ClNO/c1-2-3-8-15-26-16-21(19-11-6-7-12-23(19)26)24(27)20-13-14-22(25)18-10-5-4-9-17(18)20/h4-7,9-14,16H,2-3,8,15H2,1H3
InChi Key
IUWBHGFOHXVVKV-UHFFFAOYSA-N
Regulatory Information
DEA Exempt Notification
This product is a DEA exempt preparation of a scheduled compound - does not require DEA Controlled Substance registration or DEA 222 form. For alternate sizes please contact sales.
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $69

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    Product Description

    JWH 398 (exempt preparation) (Item No. 15686) is an analytical reference standard categorized as a synthetic cannabinoid.1 JWH 398 is regulated as a Schedule I compound in the United States. JWH 398 (exempt preparation) (Item No. 15686) is provided as a DEA exempt preparation. 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. Huffman, J.W. Cannabimimetic indoles, pyrroles, and indenes: Structure-activity relationships and receptor interactions. The cannabinoid receptors 49-95 (2009).