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JWH 398 N-pentanoic acid metabolite-d5

Item No. 14372

Synonyms
Synonyms
  • JWH 398 N-(5-carboxypentyl) metabolite-d5
Technical Information
Formal Name
5-(3-(4-chloro-1-naphthoyl)-1H-indol-1-yl-2,4,5,6,7-d5)pentanoic acid
CAS Number
2749394-76-9
Molecular Formula
C24H15ClD5NO3
Formula Weight
Purity
≥99% deuterated forms (d1-d5)
Formulation
A 1 mg/ml solution in acetonitrile
DMF: 14 mg/mlDMF:PBS (pH 7.2) (1:1): 0.5 mg/mlDMSO: 11 mg/mlEthanol: 10 mg/ml
λmax
221, 313, 419 nm
SMILES
O=C(C1=C(C=CC=C2)C2=C(Cl)C=C1)C3=C([2H])N(CCCCC(O)=O)C4=C3C([2H])=C([2H])C([2H])=C4[2H]
InChi Code
InChI=1S/C24H20ClNO3/c25-21-13-12-19(16-7-1-2-8-17(16)21)24(29)20-15-26(14-6-5-11-23(27)28)22-10-4-3-9-18(20)22/h1-4,7-10,12-13,15H,5-6,11,14H2,(H,27,28)/i3D,4D,9D,10D,15D
InChi Key
VTGKQZQQXCKOOD-SUBDTABOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    JWH 398 N-pentanoic acid metabolite-d5 is intended for use as an internal standard for the quantification of JWH 398 N-pentanoic acid metabolite by GC- or LC-MS. JWH 398 (Item No. 13636) is a synthetic cannabinoid (CB) that acts as an agonist at both the central CB1 receptor and the peripheral CB2 receptor (Kis = 2.3 and 2.8 nM, respectively).1 It has been detected as an additive of herbal mixtures.2 JWH 398 N-pentanoic acid metabolite is an expected phase I metabolite of JWH 398. The biological and toxicological properties of this compound have not been characterized. This product is intended for forensic and research purposes.

    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).

    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).