An Analytical Reference Standard
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Parent Compound(s)
ISO00122PB-22
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PB-22 3-carboxyindole metabolite

Item No. 14385

Technical Information
Formal Name
1-pentyl-1H-indole-3-carboxylic acid
CAS Number
727421-73-0
Molecular Formula
C14H17NO2
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5 mg/mlEthanol: 10 mg/ml
λmax
216, 289 nm
SMILES
O=C(O)C1=CN(CCCCC)C2=C1C=CC=C2
InChi Code
InChI=1S/C14H17NO2/c1-2-3-6-9-15-10-12(14(16)17)11-7-4-5-8-13(11)15/h4-5,7-8,10H,2-3,6,9H2,1H3,(H,16,17)
InChi Key
HAPJUNILBCTRIJ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    PB-22 (Item No. 14096) is an analog of the potent synthetic cannabinoid, JWH 018 (Item No. 10900), which differs by having 8-hydroxyquinoline replacing the naphthalene group of JWH 018.1,2 PB-22 3-carboxyindole metabolite is expected to be a metabolite of PB-22 that would be detectable both in serum and urine. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sobolevsky, T., Prasolov, I., and Rodchenkov, G. Detection of JWH-018 metabolites in smoking mixture post-administration urine. Forensic Sci. Int. 200(1-3), 141-147 (2010).

    2. Moran, C.L., Le, V.H., Chimalakonda, K.C., et alQuantitative measurement of JWH-018 and JWH-073 metabolites excreted in human urine. Anal. Chem. 83(11), 4228-4236 (2011).

    Product Citations

    Ong, R.S., Kappatos, D.C., Russell, S.G.G., et alSimultaneous analysis of 29 synthetic cannabinoids and metabolites, amphetamines, and cannabinoids in human whole blood by liquid chromatography-tandem mass spectrometry - A New Zealand perspective of use in 2018. Drug. Test. Anal. 12(2), 195-214 (2020).

    Thomas, B.F., Lefever, T.W., Cortes, R.A., et alThermolytic degradation of synthetic cannabinoids: Chemical exposures and pharmacological consequences. J. Pharmacol. Exp. Ther. 361(1), 162-171 (2017).

    Minakata, K., Hasegawa, K., Yamagishi, I., et alSensitive quantification of 5F-PB-22 and its three metabolites 5F-PB-22 3-carboxyindole, B-22 N-5-hydroxypentyl and PB-22 N-pentanoic acid in authentic urine specimens obtained from four individuals by liquid chromatography-tandem mass spectrometry. Forensic Toxicol. (2017).