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Isotodesnitazene (citrate)

Item No. 30286

Synonyms
Synonyms
  • Desnitroisotonitazene
Technical Information
Formal Name
N,N-diethyl-2-[[4-(1-methylethoxy)phenyl]methyl]-1H-benzimidazole-1-ethanamine, 2-hydroxy-1,2,3-propanetricarboxylate
Molecular Formula
C23H31N3O • C6H8O7
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 10 mg/mlDMSO: 10 mg/mlPBS (pH 7.2): 1 mg/ml
λmax
229 nm
SMILES
CCN(CC)CCN1C(CC2=CC=C(OC(C)C)C=C2)=NC3=CC=CC=C31.OC(CC(O)=O)(C(O)=O)CC(O)=O
InChi Code
InChI=1S/C23H31N3O.C6H8O7/c1-5-25(6-2)15-16-26-22-10-8-7-9-21(22)24-23(26)17-19-11-13-20(14-12-19)27-18(3)4;7-3(8)1-6(13,5(11)12)2-4(9)10/h7-14,18H,5-6,15-17H2,1-4H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)
InChi Key
KWIINCAJOQGWPO-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Isotodesnitazene (citrate) (Item No. 30286) is an analytical reference standard 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. Vandeputte, M.M., Van Uytfanghe, K., Layle, N.K., et alSynthesis, chemical characterization, and µ-opioid receptor activity assessment of the emerging group of "nitazene" 2-benzylbenzimidazole synthetic opioids. ACS Chem. Neurosci. 12(7), 1241-1251 (2021).

    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).

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

    Vandeputte, M.M., Van Uytfanghe, K., Layle, N.K., et alSynthesis, chemical characterization, and µ-opioid receptor activity assessment of the emerging group of "nitazene" 2-benzylbenzimidazole synthetic opioids. ACS Chem. Neurosci. 12(7), 1241-1251 (2021).