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4-acetoxy DiPT (acetate)

Item No. 11311

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 4-acetoxy-N,N-Diisopropyltryptamine
  • Ipracetin
Technical Information
Formal Name
3-[2-[bis(1-methylethyl)amino]ethyl]-1H-indol-4-ol, 4-acetate, monoacetate
CAS Number
2749435-22-9
Molecular Formula
C18H26N2O2 • C2H4O2
Formula Weight
362.5
Purity
≥95%
Formulation
A 10 mg/ml solution in acetonitirile
Solubility(Learn about Variance in Solubility)
DMF: 10 mg/mlDMSO: 16 mg/mlEthanol: 20 mg/mlPBS (pH 7.2): 5 mg/ml
λmax
220, 278 nm
SMILES
CC(C)N(C(C)C)CCC1=CNC2=C1C(OC(C)=O)=CC=C2.CC(O)=O
InChi Code
InChI=1S/C18H26N2O2.C2H4O2/c1-12(2)20(13(3)4)10-9-15-11-19-16-7-6-8-17(18(15)16)22-14(5)21;1-2(3)4/h6-8,11-13,19H,9-10H2,1-5H3;1H3,(H,3,4)
InChi Key
VCOMLUJEOMXDIQ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-80°C
Shipping
Dry ice in continental US; may vary elsewhere
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    Product Description

    4-acetoxy DiPT (acetate) (Item No. 11311) is an analytical reference standard categorized as a tryptamine.1 4-acetoxy DiPT induces the head-twitch response (HTR) in mice, indicating hallucinogenic potential. 4-acetoxy DiPT substitutes for DOM (Item No. 11145 | 15703) in a two-lever drug discrimination test.2 4-acetoxy DiPT has a high potential for abuse. 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. Klein, A.K., Chatha, M., Laskowski, L.J., et al. Investigation of the structure−activity relationships of psilocybin analogues. ACS Pharmacol. Transl. Sci. 4(2), 533-542 (2020).

    2. Gatch, M.B., Hoch, A., and Carbonaro, T.M. Discriminative stimulus effects of substituted tryptamines in rats. ACS Pharmacol. Transl. Sci. 4(2), 467-471 (2020).

    Product Citations

    Kozell, L.B., Eshleman, A.J., Swanson, T.L., et al. Pharmacologic activity of substituted tryptamines at 5-HT2AR, 5-HT2CR, 5-HT1AR, and SERT. J. Pharmacol. Exp. Ther. JPET-AR-2022-001454 (2023).

    Klein, A.K., Chatha, M., Laskowski, L.J., et al. Investigation of the structure−activity relationships of psilocybin analogues. ACS Pharmacol. Transl. Sci. 4(2), 533-542 (2020).

    Elmhurst, J.L., Betti, P.A., and Rangachari, P.K. Intestinal effects of isoprostanes: Evidence for the involvement of prostanoid EP and TP receptors. J. Pharmacol. Exp. Ther. 283, 1198-1205 (1997).