An Analytical Reference Material
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  • 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
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MMB-FUBINACA

Item No. 9001960

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • ​AMB-FUBINACA
  • FUB-AMB
Technical Information
Formal Name
N-[[1-[(4-fluorophenyl)methyl]-1H-indazol-3-yl]carbonyl]-L-valine, methyl ester
CAS Number
1971007-92-7
Molecular Formula
C21H22FN3O3
Formula Weight
383.4
Purity
≥98%
Formulation
A neat solid
SMILES
FC(C=C1)=CC=C1CN2N=C(C(N[C@H](C(OC)=O)C(C)C)=O)C3=CC=CC=C32
InChi Code
InChI=1S/C21H22FN3O3/c1-13(2)18(21(27)28-3)23-20(26)19-16-6-4-5-7-17(16)25(24-19)12-14-8-10-15(22)11-9-14/h4-11,13,18H,12H2,1-3H3,(H,23,26)/t18-/m0/s1
InChi Key
FRFFLYJQPCIIQB-SFHVURJKSA-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

    MMB-FUBINACA (Item No. 9001960) is an analytical reference material categorized as a synthetic cannabinoid.1 MMB-FUBINACA 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

    Patel, M., Ganeshan, D., Horgan, I., et al. AB-MDMSBA—not a synthetic cannabinoid receptor agonist. Pharmacol. Res. Perspect. 14:e70278 (2026).

    Mohamed Masoud, K.M., Syed, S.M., and Alasiri, A.M. Analyte protectant approach to protect amide-based synthetic cannabinoids from degradation and esterification during GC-MS analysis. J. Chromatogr. A. 1730, 465022 (2024).

    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).

    Schoeder, C.T., Hess, C., Madea, B., et al. Pharmacological evaluation of new constituents of "Spice": Synthetic cannabinoids based on indole, indazole, benzimidazole and carbazole scaffolds. Forensic Toxicol. 36(2), 385-403 (2018).