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
Related Products
Alternative(s)
446948β,9β-epoxy Hexahydrocannabinol (exempt preparation)
Diastereomer(s)
446938α,9α-epoxy Hexahydrocannabinol (exempt preparation)
Isomer(s)
36517(–)-7-hydroxy Cannabidiol 33076(–)-7-hydroxy Cannabidiol (CRM) 21667(±)-11-hydroxy-Δ9-THC (CRM) 41185(±)-11-hydroxy-Δ9-THC (CRM) 40854(±)-6',7'-epoxy Cannabichromene 40853(±)-8'-hydroxy Cannabichromene 29469(−)-11-hydroxy-Δ8-THC 34023(−)-11-hydroxy-Δ8-THC (CRM) 14239(−)-11-hydroxy-Δ9-THC 27576(−)-6α-hydroxy Cannabidiol 38231(6aR,9R)-11-hydroxy-Δ10-THC 41299(6aR,9R)-11-hydroxy-Δ10-THC (exempt preparation) 390241(R),2(S)-epoxy Cannabidiol 3802010α-hydroxy-exo-THC 3802210α-hydroxy-Δ8-THC 275776β-hydroxy Cannabidiol 377658α-hydroxy-exo-THC 397958α-hydroxy-exo-THC (exempt preparation) 376348α-hydroxy-Δ9-THC 397938α-hydroxy-Δ9-THC (exempt preparation) 420218α,9α-epoxy Hexahydrocannabinol 446098α,9α-epoxy Hexahydrocannabinol (exempt preparation) 377668β-hydroxy-exo-THC 397968β-hydroxy-exo-THC (exempt preparation) 376358β-hydroxy-Δ9-THC 397948β-hydroxy-Δ9-THC (exempt preparation) 399729α,10α-epoxy Hexahydrocannabinol 446109α,10α-epoxy Hexahydrocannabinol (exempt preparation) 446929α,10α-epoxy Hexahydrocannabinol (exempt preparation) 420239β,10β-epoxy Hexahydrocannabinol 446079β,10β-epoxy Hexahydrocannabinol (exempt preparation) 446959β,10β-epoxy Hexahydrocannabinol (exempt preparation) 21092Cannabielsoin 36661Cannabielsoin (CRM) 30862CBGQ36829Hexocannabitriol
Non-Exempt Preparation(s)
420228β,9β-epoxy Hexahydrocannabinol
Parent Compound(s)
35329(+)-Δ8-THC 14042Δ8-THC 41193Δ8-THC (Alt. Batch CRM) ISO60158Δ8-THC (CRM)
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8β,9β-epoxy Hexahydrocannabinol (exempt preparation)

Item No. 44608

Exempt Product (US)
Product Insert (PDF)
Synonyms
Synonyms
  • 8β,9β-EHHC
  • 8β,9β-epoxy HHC
Technical Information
Formal Name
6aR,7,7aR,8aS,9,9aR-hexahydro-6,6,8a-trimethyl-3-pentyl-6H-oxireno[4,5]benzo[1,2-c][1]benzo-1-ol
CAS Number
64783-83-1
Molecular Formula
C21H30O3
Formula Weight
330.5
Purity
≥95%
Formulation (Request formulation change)
A 1 mg/ml solution in acetonitrile
SMILES
CC1(C)[C@@]2([H])[C@](C[C@](C)(O3)[C@@]3([H])C2)([H])C4=C(C=C(CCCCC)C=C4O)O1
InChi Code
InChI=1S/C21H30O3/c1-5-6-7-8-13-9-16(22)19-14-12-21(4)18(24-21)11-15(14)20(2,3)23-17(19)10-13/h9-10,14-15,18,22H,5-8,11-12H2,1-4H3/t14-,15-,18-,21+/m1/s1
InChi Key
DIZIBWOZVJVYLY-YOZRSPHLSA-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
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $571

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    Product Description

    8β,9β-epoxy Hexahydrocannabinol (Item No. 44608) is an analytical reference standard categorized as a phytocannabinoid metabolite.1 8β,9β-epoxy Hexahydrocannabinol is an active metabolite of Δ8-THC (Item Nos. ISO60158 | 41193 | 14042). It prolongs pentobarbital-induced sleeping time in mice. 8β,9β-epoxy Hexahydrocannabinol is regulated as a Schedule I compound in the United States. 8β,9β-epoxy Hexahydrocannabinol (exempt preparation) (Item No. 44608) 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. Narimatsu, S., Watanabe, K., Shimonishi, T., et al. Metabolic disposition of 8α, 9α- and 8β, 9β-epoxyhexahydrocannabinols in the mouse. J. Pharmacobiodyn. 7(9), 671-676 (1984).