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Psilocin-d6

Item No. 34780

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 4-hydroxy-N,N-Dimethyltryptamine-d6
  • 4-hydroxy DMT-d6
Technical Information
Formal Name
3-[2-[di(methyl-d3)amino]ethyl]-1H-undol-4-ol
CAS Number
2684212-54-0
Molecular Formula
C12H10D6N2O
Formula Weight
210.3
Purity
≥99% deuterated forms (d1-d6)
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 25 mg/mlDMSO: 25 mg/mlDMSO:PBS (pH 7.2) (1:2): 025 mg/mlEthanol: 1 mg/ml
λmax
224 nm
SMILES
OC1=CC=CC2=C1C(CCN(C([2H])([2H])[2H])C([2H])([2H])[2H])=CN2
InChi Code
InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3/i1D3,2D3
InChi Key
SPCIYGNTAMCTRO-WFGJKAKNSA-N
Regulatory Information
DEA Schedule
I
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    1 mg

    $334

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    Product Description

    Psilocin-d6 (Item No. 34780) is an analytical reference standard intended for use as an internal standard for the quantification of psilocin (Item Nos. 9003135 | 11864 | 36971) by GC- or LC-MS. Psilocin is categorized as a tryptamine.1 Psilocin is the active metabolite of the psychedelic compound psilocybin (Item Nos. 9003134 | 14041) and the synthetic tryptamine 4-acetoxy DMT (psilacetin; Item Nos. 14056 | 35188).2,3 It induces the head-twitch response (HTR) in mice, indicating hallucinogenic potential.4 Psilocin 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. Blair, J.B., Kurrasch-Orbaugh, D., Marona-Lewicka, D., et al. Effect of ring fluorination on the pharmacology of hallucinogenic tryptamines. J. Med. Chem. 43(24), 4701-4710 (2000).

    2. Halberstadt, A.L., Koedood, L., Powell, S.B., et al. Differential contributions of serotonin receptors to the behavioral effects of indoleamine hallucinogens in mice. J. Psychopharmacol. 25(11), 1548-1561 (2011).

    3. Geiger, H.A., Wurst, M.G., and Daniels, R.N. DARK classics in chemical neuroscience: Psilocybin. ACS Chem. Neurosci. 9(10), 2438-2447 (2018).

    4. Glatfelter, G.C., Pottie, E., Partilla, J.S., et al. Structure–activity relationships for psilocybin, baeocystin, aeruginascin, and related analogues to produce pharmacological effects in mice. ACS Pharmacol. Transl. Sci. 5(11), 1181-1196 (2022).