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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AB-CHMINACA

Item No. 15434

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N-[(1S)-1-(aminocarbonyl)-2-methylpropyl]-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide
CAS Number
1185887-21-1
Molecular Formula
C20H28N4O2
Formula Weight
356.5
Purity
≥98%
Formulation
A neat solid
SMILES
O=C(N[C@H](C(N)=O)C(C)C)C1=NN(CC2CCCCC2)C3=C1C=CC=C3
InChi Code
InChI=1S/C20H28N4O2/c1-13(2)17(19(21)25)22-20(26)18-15-10-6-7-11-16(15)24(23-18)12-14-8-4-3-5-9-14/h6-7,10-11,13-14,17H,3-5,8-9,12H2,1-2H3,(H2,21,25)(H,22,26)/t17-/m0/s1
InChi Key
KJNZIEGLNLCWTQ-KRWDZBQOSA-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

    AB-CHMINACA (Item No. 15434) is an analytical reference material categorized as a synthetic cannabinoid.1 It has been found in Spice-type herbal blends and is associated with slurred speech, confusion, lethargy, and lack of coordination in cases of driving under the influence.2 AB-CHMINACA 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. Wurita, A., Hasegawa, K., Minakata, K., et al. Identification and quantification of metabolites of AB-CHMINACA in a urine specimen of an abuser. Leg. Med. (Tokyo) 19, 113-118 (2015).

    2. Peterson, B.L., and Couper, F.J. Concentrations of AB-CHMINACA and AB-PINACA and driving behavior in suspected impaired driving cases. J. Anal. Toxicol. 39(8), 642-647 (2015).

    Product Citations

    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).

    Mohammad, S.A., Mousa, R.E.A., Gebril, S.M., et al. Toxic effects of AB-CHMINACA on liver and kidney and detection of its blood level in adult male mice. Forensic Toxicol. (2023).

    Patel, M., Manning, J.J., Finlay, D.B., et al. Signalling profiles of a structurally diverse panel of synthetic cannabinoid receptor agonists. Biochem. Pharmacol. 175, 113871 (2020).

    Cho, B., Cho, H.S., Kim, J., et al. Simultaneous 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).

    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).

    Minakata, K., Hasegawa, K., Yamagishi, I., et al. Sensitive 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).

    Erratico, C., Negreira, N., Norouzizadeh, H., et al. In vitro and in vivo human metabolism of the synthetic cannabinoid AB-CHMINACA. Drug Test Anal. 7(10), 866-876 (2015).

    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).