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4-fluoro MDMB-BUTINACA 3-carboxyindazole metabolite

Item No. 27819

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
1-(4-fluorobutyl)-1H-indazole-3-carboxylic acid
CAS Number
2027536-90-7
Molecular Formula
C12H13FN2O2
Formula Weight
236.2
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 30 mg/mlDMSO: 20 mg/mlEthanol: 30 mg/mlEthanol:PBS (pH 7.2) (1:30): 0.03 mg/ml
λmax
300 nm
SMILES
O=C(O)C1=NN(CCCCF)C2=C1C=CC=C2
InChi Code
InChI=1S/C12H13FN2O2/c13-7-3-4-8-15-10-6-2-1-5-9(10)11(14-15)12(16)17/h1-2,5-6H,3-4,7-8H2,(H,16,17)
InChi Key
NUNURCOLPAGUIS-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $183

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    Product Description

    4-fluoro MDMB-BUTINACA 3-carboxyindazole metabolite (Item No. 27819) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. 4-fluoro MDMB-BUTINACA 3-carboxyindazole metabolite is a precursor in the synthesis of 4-fluoro MDMB-BUTINACA (Item No. 26645).1 It is a potential metabolite of 4-fluoro MDMB-BUTINACA based on the published metabolism of 5-fluoro AMB (Item No. 15489) and MDMB-PINACA.2 At the time 4-fluoro MDMB-BUTINACA 3-carboxyindazole metabolite (Item No. 27819) was made available for purchase, specific metabolism data had not been published. Contact us if updated information on this molecule is now available. 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. Cannaert, A., Sparkes, E., Pike, E., et al. Synthesis and in vitro cannabinoid receptor 1 activity of recently detected synthetic cannabinoids 4F-MDMB-BICA, 5F-MPP-PICA, MMB-4en-PICA, CUMYL-CBMICA, ADB-BINACA, APP-BINACA, 4F-MDMB-BINACA, MDMB-4en-PINACA, A-CHMINACA, 5F-AB-P7AICA, 5F-MDMB-P7AICA, and 5F-AP7AICA. ACS Chem. Neurosci. 11(24), 4434-4446 (2020).

    2. 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).