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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NMT (exempt preparation)

Item No. 36744

Synonyms
Synonyms
  • Dipterine
  • N-methyl Tryptamine
Technical Information
Formal Name
N-methyl-1H-indole-3-ethanamine
CAS Number
61-49-4
Molecular Formula
C11H14N2
Formula Weight
Purity
≥98%
Formulation
A 1 mg/ml solution in methanol
λmax
222, 282 nm
SMILES
CNCCC1=CNC2=CC=CC=C21
InChi Code
InChI=1S/C11H14N2/c1-12-7-6-9-8-13-11-5-3-2-4-10(9)11/h2-5,8,12-13H,6-7H2,1H3
InChi Key
NCIKQJBVUNUXLW-UHFFFAOYSA-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

    NMT (exempt preparation) (Item No. 36744) is an analytical reference standard categorized as a tryptamine.1 It is a minor component of ayahuasca, a botanical mixture that has hallucinogenic properties.2 NMT is regulated as a Schedule I compound in the United States. NMT (exempt preparation) (Item No. 36744) 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. Schmid, C.L., and Bohn, L.M. Serotonin, but not N-methyltryptamines, activates the serotonin 2A receptor via a β-arrestin2/Src/Akt signaling complex in vivo. J. Neurosci. 30(40), 13513-13524 (2010).

    2. Riba, J., Mcllhenny, E.H., Valle, M., et alMetabolism and disposition of N,N-dimethyltryptamine and harmala alkaloids after oral administration of ayahuasca. Drug Test Anal. 4(7-8), 610-616 (2012).