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JWH 122 N-(5-hydroxypentyl) metabolite-d5

Item No. 11475

Synonyms
Synonyms
  • MAM2201 N-(5-hydroxypentyl) metabolite-d5
Technical Information
Formal Name
[1-(5-hydroxypentyl)-1H-indol-3-yl-2,4,5,6,7-d5](4-methyl-1-naphthalenyl)-methanone
CAS Number
2749387-95-7
Molecular Formula
C25H20D5NO2
Formula Weight
Purity
≥99% deuterated forms (d1-d5)
Formulation
A 1 mg/ml solution in methanol
DMF: 10 mg/mlDMSO: 12.5 mg/mlEthanol: 10 mg/ml
λmax
221, 246, 316 nm
SMILES
O=C(C1=CC=C(C)C2=C1C=CC=C2)C3=C([2H])N(CCCCCO)C4=C([2H])C([2H])=C([2H])C([2H])=C43
InChi Code
InChI=1S/C21H22ClNO2/c1-15(24)7-6-12-23-14-18(17-9-3-5-11-20(17)23)21(25)13-16-8-2-4-10-19(16)22/h2-5,8-11,14-15,24H,6-7,12-13H2,1H3/i3D,5D,9D,11D,14D
InChi Key
ALUOSHHIHVCMCU-QMJOWLLBSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    JWH 122 N-(5-hydroxypentyl) metabolite-d5 contains five deuterium atoms at the 2, 4 ,5, 6, and 7 positions. It is intended for use as an internal standard for the quantification of JWH 122 N-(5-hydroxypentyl) metabolite (Item No. 10925) by GC- or LC-mass spectrometry. JWH 122 is a synthetic cannabinoid (CB) of the naphthoylindole class that is structurally related to JWH 018 and JWH 073. It displays high-affinities for both CB1 (Ki = 0.69 nM) and CB2 (Ki = 1.2 nM) receptors.1,2 JWH 122 N-(5-hydroxypentyl) metabolite is a metabolite of JWH 122 (Item No. 10591) that is characterized by monohydroxylation of the N-alkyl chain. Currently, there are no reports of its biological activity.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ernst, L., Schiebel, H.M., Theuring, C., et alIdentification and characterization of JWH-122 used as new ingredient in "spice-like" herbal incenses. Forensic Sci. Int. 208(1-3), e31-e35 (2011).

    2. Kikura-Hanajiri, R., Uchiyama, N., and Goda, Y. Survey of current trends in the abuse of psychotropic substances and plants in Japan. Leg. Med. (Tokyo) 13(3), 109-115 (2011).