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(-JWH 398 N-(4-hydroxypentyl) metabolite-d5

CAS No.
2747914-17-4
Chemical Name:
(-JWH 398 N-(4-hydroxypentyl) metabolite-d5
Synonyms
(-JWH 398 N-(4-hydroxypentyl) metabolite-d5;(±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5;(4-chloronaphthalen-1-yl)(1-(4-hydroxypentyl)-1H-indol-3-yl-2,4,5,6,7-d5)methanone
CBNumber:
CB04665597
Molecular Formula:
C24H17D5ClNO2
Molecular Weight:
396.93
MDL Number:
MOL File:
2747914-17-4.mol
MSDS File:
SDS
Last updated:2025-08-21 11:10:19

(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 Properties

solubility DMF: 20 mg/ml
DMSO: 25 mg/ml
Ethanol: 15 mg/ml

(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 14370 (±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5 ≥99%deuteratedforms(d1-d5) 2747914-17-4 500μg $169 2026-04-30 Buy
Cayman Chemical 14370 (±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5 ≥99%deuteratedforms(d1-d5) 2747914-17-4 1mg $319 2026-04-30 Buy
aablocks AA01EP0R (±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5 ≥99%deuteratedforms(d1-d5) 2747914-17-4 1mg $319 2026-05-30 Buy
Product number Packaging Price Buy
14370 500μg $169 Buy
14370 1mg $319 Buy
AA01EP0R 1mg $319 Buy

(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 Chemical Properties, Uses, Production

Description

(±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5 (Item No. 14370) is intended for use as an internal standard for the quantification of JWH 398 N-(4-hydroxypentyl) metabolite (Item No. 10943) by GC- or LC-MS. JWH 398 (Item No. 13636) is a synthetic cannabinoid (CB) that activates both central CB1 and peripheral CB2 receptors (Ki = 2.3 and 2.8 nM, respectively).1 It has been reported to be an adulterant of herbal products.2,3 (±)-JWH 398 N-(4-hydroxypentyl) metabolite is an expected phase I metabolite of JWH 398 (Item No. 13636), detectable in serum and urine. While similar hydroxylated phase I metabolites of synthetic CBs retain activity, the physiological properties of this compound have yet to be determined.4,5 This product is intended for research and forensic applications.WARNING This product is not for human or veterinary use.

References

[1] HUFFMAN J. Cannabimimetic Indoles, Pyrroles, and Indenes: Structure–Activity Relationships and Receptor Interactions[C]. 1900: 0. DOI: 10.1007/978-1-59745-503-9_3
[2] RURI KIKURA-HANAJIRI  Yukihiro G  Nahoko Uchiyama. Survey of current trends in the abuse of psychotropic substances and plants in Japan[J]. Legal Medicine, 2011, 13 3: Pages 109-115. DOI: 10.1016/j.legalmed.2011.02.003
[3] SEBASTIAN DRESEN. Monitoring of herbal mixtures potentially containing synthetic cannabinoids as psychoactive compounds[J]. Journal of Mass Spectrometry, 2010, 45 10: 1186-1194. DOI: 10.1002/jms.1811
[4] LISA K BRENTS. Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity.[J]. PLoS ONE, 2011: e21917. DOI: 10.1371/journal.pone.0021917
[5] LISA K. BRENTS . Monohydroxylated metabolites of the K2 synthetic cannabinoid JWH-073 retain intermediate to high cannabinoid 1 receptor (CB1R) affinity and exhibit neutral antagonist to partial agonist activity[J]. Biochemical pharmacology, 2012, 83 7: Pages 952-961. DOI: 10.1016/j.bcp.2012.01.004

(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 Preparation Products And Raw materials

Raw materials

Preparation Products

(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 Suppliers

Global Suppliers ( 6)
Supplier Tel Email Country ProdList Advantage
Cayman Chemical Company -- sales@caymanchem.com China 6808 58
United States Biological -- sales@advtechind.com United States 6035 58
Cayman Chemical Company -- cayman@caymanchem.com United States 6987 81
United States Biological -- chemicals@usbio.net United States 6131 80
Toronto Research Chemicals Inc. -- info@trc-canada.com Canada 6661 58
Medical Isotopes, Inc -- info@medicalisotopes.com United States 3178 58
(-JWH 398 N-(4-hydroxypentyl) metabolite-d5 (4-chloronaphthalen-1-yl)(1-(4-hydroxypentyl)-1H-indol-3-yl-2,4,5,6,7-d5)methanone (±)-JWH 398 N-(4-hydroxypentyl) metabolite-d5 2747914-17-4 C24H17D5ClNO2