Basic information Safety Supplier Related

5-Methyltryptamine hydrochloride

Basic information Safety Supplier Related

5-Methyltryptamine hydrochloride Basic information

Product Name:
5-Methyltryptamine hydrochloride
Synonyms:
  • 5-METHYLTRYPTAMNE HCL 98.0%MIN
  • 2-(5-METHYL-1H-INDOL-3-YL)ETHYLAMINE HYDROCHLORIDE
  • 2-(5-METHYL-1H-INDOL-3-YL)ETHANAMINE HYDROCHLORIDE
  • 2-[5-METHYLINDOL-3-YL]ETHYLAMINE HYDROCHLORIDE
  • 3-(2-AMINOETHYL)-5-METHYLINDOLE HYDROCHLORIDE
  • 3-(2-AMINOETHYL)-5-METHYLINDOLE HCL
  • 5-METHYLTRYPTAMINE HCL
  • 5-METHYLTRYPTAMINE HYDROCHLORIDE
CAS:
1010-95-3
MF:
C11H15ClN2
MW:
210.7
EINECS:
213-777-8
Mol File:
1010-95-3.mol
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5-Methyltryptamine hydrochloride Chemical Properties

Melting point:
290-292 °C
solubility 
DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form 
Solid
color 
Pale Beige to Light Tan
Sensitive 
Hygroscopic
CAS DataBase Reference
1010-95-3
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Safety Information

Hazard Codes 
T+
Risk Statements 
26/27/28
Safety Statements 
22-24/25
RIDADR 
2811
WGK Germany 
3
10
HazardClass 
6.1
PackingGroup 

MSDS

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5-Methyltryptamine hydrochloride Usage And Synthesis

Chemical Properties

Light Tan Solid

Uses

  • reactant in synthesis of kinesin spindle protein (KSP) inhibitors
  • reactant in intramolecular furan Diels-Alder reactions
  • reactant in Pictet-Spengler-like reactions

Uses

5-Methyltryptamine hydrochloride is a methylated derivative of tryptamine, it is a weak antagonist of 5-Hydroxytryptamine (H974990) with weak potency as stimulants of the cardiac sympathetic nerves. 5-Methyltryptamine hydrochloride is also used in the preparation of inhibitors of kinesin spindle protein (KSP), a promising class of anticancer agents.

Purification Methods

Recrystallise the hydrochloride from H2O. The free base has m 96-98o (from *C6H6/cyclohexane) or m 99-100o (from pet ether), and the picrate has m 243o(dec) (from EtOH). [Young J Chem Soc 3493 1958, Gaddum et al. Quart J Exp Physiol 40 49 1955, R.hm Hoppe Seyler's Z Physiol Chem 297 229 1954, Beilstein 22 III/IV 4364, 22/10 V 167.]

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