06840
1-Methyltryptamine
≥95.0% (GC)
Synonym(s):
1-Methyl-1H-indole-3-ethanamine, 1-Methyl-3-(2-aminoethyl)indole, 2-(1-Methyl-1H-indol-3-yl)ethylamine, N1-Methyltryptamine, NMT
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C11H14N2
CAS Number:
Molecular Weight:
174.24
UNSPSC Code:
12352200
NACRES:
NA.25
PubChem Substance ID:
EC Number:
231-377-1
Beilstein/REAXYS Number:
6874
MDL number:
InChI
1S/C11H14N2/c1-13-8-9(6-7-12)10-4-2-3-5-11(10)13/h2-5,8H,6-7,12H2,1H3
InChI key
CAAGZPJPCKMFBD-UHFFFAOYSA-N
SMILES string
Cn1cc(CCN)c2ccccc12
assay
≥95.0% (GC)
form
liquid
color
light yellow
Quality Level
Biochem/physiol Actions
Metabolite in N-methyltransferase metabolism of tryptamine and decarboxylation of 1-methyltryptophan.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
E M Adkins et al.
Molecular pharmacology, 59(3), 514-523 (2001-02-17)
The serotonin (5-hydroxytryptamine, 5-HT) transporter (SERT) is responsible for the inactivation of synaptic 5-HT and is also a target for multiple psychostimulants. Despite the critical role of SERT in 5-HT inactivation and psychostimulant response, many aspects of the transporter's recognition
N-methylation of 1-methyltryptamines by indolethylamine N-methyltransferase.
R Lin et al.
Biochemical pharmacology, 24(11-12), 1239-1240 (1975-06-15)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service