An Analytical Reference Standard
Features
  • This product has been formulated as an exempt preparation which meets criteria established by the US DEA
  • Possession of a DEA Controlled Substance registration is not necessary nor is a DEA 222 form required to purchase this product
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing
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Psilocybin-d10 (exempt preparation)

Item No. 40356

Technical Information
Formal Name
3-[2-((dimethyl-d3)amino)ethyl-1,1,2,2-d4]-1H-indol-4-ol, 4-(dihydrogen phosphate)
CAS Number
2641522-10-1
Molecular Formula
C12H7D10N2O4P
Formula Weight
Purity
≥99% deuterated forms (d1-d10)
Formulation
A 100 µg/ml solution in acetonitrile:water (1:1)
SMILES
O=P(O)(O)OC1=CC=CC2=C1C(C([2H])([2H])C([2H])([2H])N(C([2H])([2H])[2H])C([2H])([2H])[2H])=CN2
InChi Code
InChI=1S/C12H17N2O4P/c1-14(2)7-6-9-8-13-10-4-3-5-11(12(9)10)18-19(15,16)17/h3-5,8,13H,6-7H2,1-2H3,(H2,15,16,17)/i1D3,2D3,6D2,7D2
InChi Key
QVDSEJDULKLHCG-HXOHQZFQSA-N
Regulatory Information
DEA Exempt Notification
This product is a DEA exempt preparation of a scheduled compound - does not require DEA Controlled Substance registration or DEA 222 form. For alternate sizes please contact sales.
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Psilocybin-d10 (exempt preparation) (Item No. 40356) is intended for use as an internal standard for the quantification of psilocybin (Item Nos. 9003134 | 14041) by GC- or LC-MS. Psilocybin is categorized as a tryptamine.1,2 It induces the head-twitch response (HTR) in mice, indicating hallucinogenic potential.2 Psilocybin-d10 is regulated as a Schedule I compound in the United States. Psilocybin-d10 (exempt preparation) (Item No. 40356) is provided as a DEA exempt preparation. 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. Nichols, D.E., and Frescas, S. Improvements to the synthesis of psilocybin and a facile method for preparing the O-acetyl prodrug of psilocin. Synthesis 6, 935-938 (1999).

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