An Analytical Reference Material
Features
  • This product is qualified as a Reference Material that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
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PB-22

Item No. ISO00122

GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • QUPIC
Technical Information
Formal Name
1-pentyl-1H-indole-3-carboxylic acid, 8-quinolinyl ester
CAS Number
1400742-17-7
Molecular Formula
C23H22N2O2
Formula Weight
Purity
≥98%
Formulation
A neat solid
SMILES
O=C(OC1=C(N=CC=C2)C2=CC=C1)C3=CN(CCCCC)C4=C3C=CC=C4
InChi Code
InChI=1S/C23H22N2O2/c1-2-3-6-15-25-16-19(18-11-4-5-12-20(18)25)23(26)27-21-13-7-9-17-10-8-14-24-22(17)21/h4-5,7-14,16H,2-3,6,15H2,1H3
InChi Key
ZAVGICCEAOUWFM-UHFFFAOYSA-N
Regulatory Information
DEA Schedule
I
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. ISO00122) is an analytical reference material categorized as a synthetic cannabinoid.1 It mimics the effects of Δ9-THC (Item Nos. 12068 | ISO60157).1 PB-22 is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Banister, S.D., Stuart, J., Kevin, R.C., et alEffects of bioisosteric fluorine in synthetic cannabinoid designer drugs JWH-018, AM-2201, UR-144, XLR-11, PB-22, 5F-PB-22, APICA, and STS-135. ACS Chem. Neurosci. 6(8), 1445-1458 (2015).

    Product Citations

    Cho, B., Cho, H.S., Kim, J., et alSimultaneous determination of synthetic cannabinoids and their metabolites in human hair using LC-MS/MS and application to human hair. Forensic Sci. Int. 306, 110058 (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).