An Analytical Reference Material
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  • This product is a qualified Reference Material that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards for reference materials
  • This product is intended to be used as an analytical reference standard
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(S)-5-fluoro ADB

Item No. 23631

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • (S)-5-fluoro MDMB-PINACA
Technical Information
Formal Name
N-[[1-(5-fluoropentyl)-1H-indazol-3-yl]carbonyl]-3-methyl-L-valine, methyl ester
CAS Number
1971007-89-2
Molecular Formula
C20H28FN3O3
Formula Weight
377.5
Purity
≥98%
Formulation
A neat solid
SMILES
O=C(N[C@H](C(OC)=O)C(C)(C)C)C1=NN(CCCCCF)C2=C1C=CC=C2
InChi Code
InChI=1S/C20H28FN3O3/c1-20(2,3)17(19(26)27-4)22-18(25)16-14-10-6-7-11-15(14)24(23-16)13-9-5-8-12-21/h6-7,10-11,17H,5,8-9,12-13H2,1-4H3,(H,22,25)/t17-/m1/s1
InChi Key
PWEKNGSNNAKWBL-QGZVFWFLSA-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

    (S)-5-fluoro ADB (Item No. 23631) is an analytical reference material categorized as a synthetic cannabinoid.1 It is the (S)-enantiomer of (R)-5-fluoro ADB (Item No. 16603). (S)-5-fluoro ADB 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., Longworth, M., Kevin, R., et al. Pharmacology of valinate and tert-leucinate synthetic cannabinoids 5F-AMBICA, 5F-AMB, 5F-ADB, AMB-FUBINACA, MDMB-FUBINACA, MDMB-CHMICA, and their analogues. ACS Chem. Neurosci. 7(9), 1241-1254 (2016).

    Product Citations

    Franz, F., Jechle, H., Wilde, M., et al. Structure-metabolism relationships of valine and tert-leucine-derived synthetic cannabinoid receptor agonists: A systematic comparison of the in vitro phase I metabolism using pooled human liver microsomes and high-resolution mass spectrometry. Forensic Toxicol. 37, 316-329 (2019).