A Certified Reference Material
Features
  • This product is qualified as a Certified Reference Material (CRM) that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This CRM has been characterized by metrologically valid procedures and may be used as a quantitative analytical reference standard
  • Certificate of analysis provides the certified property values and the associated uncertainties, including a statement of metrological traceability for the certified values
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
Related Products
Analytical Standard(s)
336704-hydroxy TMT (iodide)
Isomer(s)
37638Bufotenidine (iodide)
Parent Compound(s)
31582Aeruginascin 37762Aeruginascin (CRM)
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4-hydroxy TMT (iodide) (CRM)

A 1 mg/ml solution in acetonitrile:water (1:1)

Item No. 38032

Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 4-hydroxy-N,N,N-Trimethyltryptamine
Technical Information
Formal Name
4-hydroxy-N,N,N-trimethyl-1H-indole-3-ethanaminium, monoiodide
CAS Number
2451455-99-3
Molecular Formula
C13H19N2O • I
Formula Weight
346.2
Formulation
A 1 mg/ml solution in acetonitrile:water (1:1)
SMILES
C[N+](C)(C)CCC1=CNC2=CC=CC(O)=C21.[I-]
InChi Code
InChI=1S/C13H18N2O.HI/c1-15(2,3)8-7-10-9-14-11-5-4-6-12(16)13(10)11;/h4-6,9,14H,7-8H2,1-3H3;1H
InChi Key
QNUXJABHEYPNKW-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $258

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    Product Description

    4-hydroxy TMT (iodide) (CRM) (Item No. 38032) is a certified reference material categorized as a tryptamine.1 4-hydroxy TMT is an active metabolite of aeruginascin (Item Nos. 37762 | 31582). It does not induce the head-twitch response (HTR) in mice.2 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. Chadeayne, A.R., Pham, D.N.K., Reid, B.G., et al. Active metabolite of aeruginascin (4-hydroxy-N,N,N-trimethyltryptamine): Synthesis, structure, and serotonergic binding affinity. ACS Omega 5(27), 16940-16943 (2020).

    2. 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).