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RANDOX Synthetic Cannabinoids ((JWH-018 / AM-2201)*

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R-JWH-018 RANDOX Synthetic Cannabinoids ((JWH-018 / AM-2201)* EA call for price none
Introduction:

JWH-018 is a synthetic cannabinoid which became commercially popular in 2008 when it was identified as one of the main active ingredients in herbal blends such as 'Spice'. JWH-018 is not structurally related to marijuana however it binds to the same cannabinoid receptor in the brain. Initial studies of the metabolism of JWH have highlighted metabolic processes such as ring and alkyl substituent hydroxylation, carboxylation and glucuronidation. The risk of accidental overdose and severe psychiatric complications may be more likely to occur as the type and amount of active compound may vary considerably from batch to batch. Reported adverse effects include agitation, rapid heart rate, confusion, dizziness and nausea.

Cross Reactivity

Analyte Compound
Cross Reactivity %
Synthetic Cannabinoids JWH-018 / AM-2001
LOD: 2.5 ng/mL
 JWH-018 100
4-OH JWH-018 (JWH-018 4-hydroxyindole)
9
5-OH JWH-018 (JWH-018 5-hydroxyindole metabolite)
56
 
6-OH JWH-018 (JWH-018 6 hydroxyindole metabolite)
215
 
7-OH JWH-018 (JWH-018 7-hydroxyindole metabolite)
89
 
N-desalkyl JWH-018: LK1012 10CD194
3
 
(±)-JWH-018 N-(4-hydroxypentyl) metabolite
195
 
JWH-018 N-(5-hydroxypentyl) metabolite
231
 
JWH-018 N-pentanoic acid metabolite
85
 
JWH-018 N-(1-methylbutyl) isomer
54
 
JWH-018 N-(1,2-dimethylpropyl) isomer
70
 
JWH- 018 N-(2,2-dimethylpropyl) isomer
62
 
JWH-018 6-methoxyindole analogue
95
 
JWH-018 N-(2-methylbutyl) isomer (JWH-073 2-methylbutyl homologue)
78
 
JWH 018 N-(3-methylbutyl) isomer (JWH-073 3-methylbutyl homologue)
217
 
JWH 018 2'-napthyl-N-(3-methylbutyl)isomer
2
 
JWH-018 (5'-Carboxy)
206
 
JWH-018 (1-(4-Carboxybutyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone(N-carboxybutyl)
133
 
JWH-073
135
 
4-OH JWH-073 (JWH-073 4-hydroxyindole metabolite)
15
 
5-OH JWH-073 (JWH-073 5-hydroxyindole metabolite)
135
 
6-OH JWH-073 (JWH-073 6-hydroxyindole metabolite)
162
 
7-OH JWH-073 (JWH-073 7-hydroxyindole metabolite)
113
 
JWH-073 n-(3-hydroxybutyl) metabolite
164
 
JWH-073 N-(4-hydroxybutyl) metabolite
255
 
JWH-073 N-Butanol
96
 
JWH-073 N-Butanoic acid metabolite
37
 
JWH-073 4 Butanoic Acid
38
 
JWH-073 2-methylnaphthyl analogue
14
 
JWH-073 4-methylnaphthyl analogue
10
 
JWH-073 N-(2-methylpropyl) isomer
113
 
JWH-007
2
 
JWH-015
3
 
JWH-016
3
 
JWH-019
35
 
JWH 019 5-hydroxyindole metabolite (JWH-019-M2)
38
 
JWH-020
22
 
JWH-022
102
 
JWH-030
6
 
JWH-081 2-methoxynaphthyl isomer or (JWH-267)
3
 
JWH-081 5-methoxynaphthyl isomer
6.5
 
JWH-081 7-methoxynaphthyl isomer (JWH-164)
5
 
JWH-081 N-(5-hydroxypentyl) metabolite
3
 
JWH-122
10
 
JWH 122 6-methylnaphthyl isomer
7
 
JWH 122 7-methylnaphthyl isomer
13
 
JWH 122 2-methylnaphthyl isomer
12
 
JWH-122 N-(5-hydroxypentyl) metabolite
16
 
JWH-147
4
 
JWH-164 (JWH-081 7-methoxynaphthyl isomer)
1.7
 
JWH-200 4-hydroxyindole metabolite
3
 
JWH-200 5-hydroxyindole metabolite
63
 
JWH-200 6-hydroxyindole metabolite
133
 
JWH-210 2-ethylnaphthyl isomer
2
 
JWH-210 7-ethylnaphthyl isomer or JWH-234
2
 
JWH-398
12
 
JWH-398 5-chloronaphthyl isomer
5
 
JWH-398 N-(5-hydroxypentyl) metabolite
36
 
AM-694
5
 
AM-694 3-iodo isomer
1
 
AM-1220
179
 
AM-2201
119
 
AM-2201 N-(4-fluoropentyl) isomer
176
 
AM-2201 N-(4-hydroxypentyl) metabolite
145
 
AM-2233
7
 
RCS-4 2-methoxy isomer
2
 
RCS-4 3-methoxy isomer
1
 
(+)WIN 55212-2 (mesylate)
2
 
WIN 55212-3 mesylate
3
 
WIN 55225 (other name JWH-200)
127
 
2-OH JWH-018 (JWH-018 2-hydroxyindole metabolite)
<1
 
JWH 018 2'-naphthyl isomer
<1
 
JWH 018 adamantyl analogue
<1
 
JWH 018 2'-naphthyl-N-(1-methylbutyl) isomer
<1
 
JWH 018 2'-naphthyl-N-(1,2-dimethylpropyl) isomer
<1
 
JWH 018 2'-naphthyl-N-(2-methylbutyl) isomer
<1
 
JWH 018 2'-naphthyl-N-(2,2-dimethylpropyl) isomer
<1
 
2-OH JWH-073 (JWH-073 2-hydroxyindole metabolite)
<1
 
JWH 073 2'-naphthyl-N-(1-methylpropyl) isomer
<1
 
JWH 073 2'-naphthyl-N-(2-methylpropyl) isomer
<1
 
JWH-011
<1
 
JWH-081
<1
 
JWH-098
<1
 
JWH-133
<1
 
JWH-182
<1
 
JWH-200 2'naphthyl isomer
<1
 
JWH-201
<1
 
JWH-203
<1
 
JWH 203 3-chloro isomer (JWH-237)
<1
 
JWH-206 (JWH-203 4-chloro isomer)
<1
 
JWH-210
<1
 
JWH-210 N-(5-carboxypentyl) metabolite
<1
 
JWH-210 5-hydroxyindole metabolite
<1
 
JWH-250
<1
 
JWH 250 N-(5-hydroxypentyl) metabolite
<1
 
JWH 250 N-(5-carboxypentyl) metabolite
<1
 
JWH 250 5-hydroxyindole metabolite
<1
 
JWH 250 5-hydroxyindole metabolite
<1
 
JWH-251
<1
 
JWH 251 3-methylphenyl isomer
<1
 
JWH-302
<1
 
AM251
<1
 
AM-630 (other name 6-Iodopravadoline)
<1
 
AM-694 4-iodo isomer
<5
 
AM-1241
<1
 
(S)-AM1241
<1
 
AM2201 2'-naphthyl isomer
<1
 
CB-13
<1
 
CB-25
<1
 
CB-52
<1
 
CB-86
<1
 
CP-49,497-C7 ((+-) CP47,497)
<1
 
CP-47,497-para-quinone analogue
<1
 
CP-49,497-C8-homologue ((+- CP) 47,497-C8-homologue)
<1
 
((+-)-CP 55,940)
<1
 
(-)-CP 55,940
<1
 
(+)-CP 55,940
<1
 
HU-210
<1
 
HU-211 (Dexanabinol)
<1
 
HU-308
<1
 
RCS-4
<1
 
RCS-4
<1
 
RCS-4-C4 homologue (BTM-4,SR-19, OBT-199, E-4)
<1
 
RCS-4 N-(4-hydroxypentyl) metabolite
<1
 
RCS-4 N-(5-hydroxypentyl) metabolite
<1
 
RCS-8 (SR-18)
<1
 
RCS-8 3-methoxy isomer
<1
 
RCS-8 4-methoxy isomer
<1
 
WIN-48,098
<1

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