Key Documents

View All Documentation

134228

5-Methyltryptamine hydrochloride

Name: 5-Methyltryptamine hydrochloride
Brand: ALDRICH

98%

Synonym(s):

3-(2-Aminoethyl)-5-methylindole hydrochloride

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₄N₂ · HCl

CAS Number:

1010-95-3

Molecular Weight:

210.70

NACRES:

NA.22

PubChem Substance ID:

24848138

UNSPSC Code:

12352100

EC Number:

213-777-8

MDL number:

MFCD00012683

Assay:

98%

Form:

powder

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

98%

form

powder

mp

289-292 °C (dec.) (lit.)

solubility

H₂O: soluble 50 mg/mL, clear, yellow

functional group

amine

SMILES string

Cl.Cc1ccc2[nH]cc(CCN)c2c1

InChI

1S/C11H14N2.ClH/c1-8-2-3-11-10(6-8)9(4-5-12)7-13-11;/h2-3,6-7,13H,4-5,12H2,1H3;1H

InChI key

RBHDFGBPJGEYCK-UHFFFAOYSA-N

Description

Application

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

5-Methyltryptamine hydrochloride was used to study the mechanism of metabolism of 9-methyl 1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine in rats. It was used as internal standard in the determination of urinary metabolites of 5-methoxy-N,N-diisopropyltryptamine in humans. It was used as reactant in:

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ruan, X., et al.

Huaxue Xuebao, 66, 1731-1731 (2008)

"Pictet-Spengler-like" Synthesis of Tetrahydro-beta-carbolines under Hydrolytic Conditions. Direct Use of Azalactones as Phenylacetaldehyde Equivalents.

James E. Audia et al.

The Journal of organic chemistry, 61(22), 7937-7939 (1996-11-01)

Detection and mass spectrometric characterization of the major urinary and fecal metabolites of 9-methyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]-quinolizine in the rat.

A Sparatore et al.

European journal of drug metabolism and pharmacokinetics, 20(2), 135-144 (1995-04-01)

The metabolic fate of 9-methyl 1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine (MIQ), a compound with promising pharmacological action on the CNS system, was investigated in the rat after an oral dose of 200 mg/kg, the maximal tolerated dose. Urine and feces were collected, exhaustively extracted

View All Related Papers

Global Trade Item Number

SKU	GTIN
134228-250MG	04061832841540