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AB-PINACA N-(4-fluoropentyl) isomer

Item No. 15441

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • AB-PINACA N-(4-fluoropentyl) analog
  • 4-fluoro AB-PINACA
Technical Information
Formal Name
N-[1-(aminocarbonyl)-2-methylpropyl]-1-(4-fluoropentyl)-1H-indazole-3-carboxamide
CAS Number
2748160-98-5
Molecular Formula
C18H25FN4O2
Formula Weight
348.4
Purity
≥95%
Formulation
A 1 mg/ml solution in methanol
Solubility(Learn about Variance in Solubility)
DMF: 10 mg/mlDMSO: 10 mg/mlDMSO:PBS (pH 7.2) (1:8): 0.1 mg/mlEthanol: 10 mg/ml
λmax
209, 302 nm
SMILES
O=C(NC(C(N)=O)C(C)C)C1=NN(CCCC(F)C)C2=C1C=CC=C2
InChi Code
InChI=1S/C18H25FN4O2/c1-11(2)15(17(20)24)21-18(25)16-13-8-4-5-9-14(13)23(22-16)10-6-7-12(3)19/h4-5,8-9,11-12,15H,6-7,10H2,1-3H3,(H2,20,24)(H,21,25)
InChi Key
KSBISSAWUAIQIT-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    AB-PINACA (Item No. 14038) is a synthetic cannabinoid recently identified in illegal herbal products.1 Structurally, this designer drug is developed on an indazole base, which distinguishes it from the many JWH compounds having an indolyl base.1,2 AB-PINACA N-(4-fluoropentyl) isomer is a derivative of AB-PINACA featuring a fluorine atom added to the pentyl group. The physiological and toxicological properties of this compound have not been determined. 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. Uchiyama, N., Matsuda, S., Wakana, D., et al. New cannabimimetic indazole derivatives, N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide (AB-PINACA) and N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide (AB-FUBINACA) identified as designer drugs in illegal products. Forensic Toxicol. 31(1), 93-100 (2013).

    2. Huffman, J.W., Zengin, G., Wu, M.J., et al. Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB1 and CB2 receptors: Steric and electronic effects of naphthoyl substituents. New highly selective CB2 receptor agonists. Bioorg. Med. Chem. 13(1), 89-112 (2005).