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N-Pyrrolidino Isotonitazene (citrate)

Item No. 34909

Synonyms
Synonyms
  • Isotonitazepine
  • Isotonitazepyne
Technical Information
Formal Name
2-(4-isopropoxybenzyl)-5-nitro-1-(2-(pyrrolidin-1-yl)ethyl)-1H-benzo[d]imidazole, 2-hydroxy-1,2,3-propanetricarboxylate
Molecular Formula
C23H28N4O3 • C6H8O7
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 10 mg/mlDMSO: 10 mg/mlPBS (pH 7.2): 1 mg/ml
λmax
240 nm
SMILES
CC(C)[O]C1=CC=C(C=C1)CC2=[N]C3=CC([N+]([O-])=O)=CC=C3[N]2CCN4CCCC4.OC(CC(O)=O)(C(O)=O)CC(O)=O
InChi Code
InChI=1S/C23H28N4O3.C6H8O7/c1-17(2)30-20-8-5-18(6-9-20)15-23-24-21-16-19(27(28)29)7-10-22(21)26(23)14-13-25-11-3-4-12-25;7-3(8)1-6(13,5(11)12)2-4(9)10/h5-10,16-17H,3-4,11-15H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)
InChi Key
XZGLLCLVIOGQGU-UHFFFAOYSA-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

    N-Pyrrolidino isotonitazene (Item No. 34909) is an analytical reference standard that is categorized as an opioid.1 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. Kozell, L.B., Eshleman, A.J., Wolfrum, K.M., et alPharmacology of newly identified nitazene variants reveals structural determinants of affinity, potency, selectivity for mu opioid receptors. Neuropharmacology 276, 110512 (2025).

    Product Citations

    Robinson, M.J., Chen, L., Thakur, A., et alCoordinated subpocket engagement underlies nitazene potency at the μ‑opioid receptor. ACS Chem. Neurosci. (2026).

    Sapkota, R., Lomnicki, E.E., and Subedi, B. Nitazenes discharged during Super Bowl and Mardi Gras celebrations in New Orleans, USA. Environ. Sci. Tech. Lett. (2026).

    Truver, M.T., Roman, M., Gomonit, M.M., et alFatal intoxications with nitazenes: Postmortem findings, toxicology, and in vitro characterization at the μ-opioid receptor of six nitazene analogues. Arch. Toxicol. (2026).

    Leonard, A.C., Lenert-Mondou, C., Chayer, R., et alComputational design of dynamic biosensors for emerging synthetic opioids. BioRxiv (2025).

    Kriikku, P., Pelander, A., Jylhä, A., et alPost-mortem identification and toxicological findings of fluetonitazepyne and isotonitazepyne. Drug Test. Anal. 17(7), 1-6 (2025).

    Hardwick, E.K., and Davidson, J.T. Structural characterization of nitazene analogs using electrospray ionization-tandem mass spectrometry (ESI-MS/MS). Drug Test Anal. (2025).

    Kozell, L.B., Eshelman, A., J., Wolfrum, K.M., et alPharmacologic characterization of substituted nitazenes at μ, κ, and Δ opioid receptors suggests high potential for toxicity. J. Pharmacol. Exp. Ther. 389(2), 219-228 (2024).