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TRYPTAMINE HYDROCHLORIDE

Basic information Safety Supplier Related

TRYPTAMINE HYDROCHLORIDE Basic information

Product Name:
TRYPTAMINE HYDROCHLORIDE
Synonyms:
  • 2-(indol-3-yl)ethylamine hydrochloride
  • beta-indolaethylamin-chlorhydrat
  • beta-indole-ethylaminehydrochloride
  • indole-3-ethylaminehydrochloride
  • Tryptamine hydrochloride, 98+%
  • 3-(2-Aminoethyl)indoleHCl~2-(3-Indolyl)ethylamineHCl
  • TRYPTAMINE HCL
  • TRYPTAMINE HYDROCHLORIDE
CAS:
343-94-2
MF:
C10H13ClN2
MW:
196.68
EINECS:
206-446-4
Product Categories:
  • Indoles
  • Indole
  • Tryptamines
  • Heterocyclic Compounds
Mol File:
343-94-2.mol
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TRYPTAMINE HYDROCHLORIDE Chemical Properties

Melting point:
253-255 °C(lit.)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
water: soluble0.1g/10 mL, clear to slightly hazy, colorless to yellow
form 
Powder
color 
Beige to light orange
Sensitive 
Light Sensitive
Merck 
14,9796
BRN 
3568419
Stability:
Hygroscopic
CAS DataBase Reference
343-94-2(CAS DataBase Reference)
EPA Substance Registry System
1H-Indole-3-ethanamine, monohydrochloride (343-94-2)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-20/21/22-41-37/38-22
Safety Statements 
22-24/25-36/37/39-36-26
WGK Germany 
3
RTECS 
NL4375000
3-8-10
TSCA 
Yes
HS Code 
29339900

MSDS

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TRYPTAMINE HYDROCHLORIDE Usage And Synthesis

Chemical Properties

beige to light orange powder

Uses

Reactant for preparation of:

  • Tryptamine derivatives as inhibitors against hepatitis B virus
  • Carbamoyl epipodophyllotoxins as potential antitumor agents
  • Anthranilic acid derivatives as CCK receptor antagonists
  • Brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors
  • Antispasmodic agents
  • β-carbolinium cations as new antimalarial agents

General Description

The fluorescence property of tryptamine hydrochloride was studied in reverse micelles solution made with benzylhexadecyldimethylammonium chloride (BHDC) in benzene.

Purification Methods

Crystallise the salt from EtOH/water or EtOH/Et2O. See previous entry for UV. [Beilstein 22 II 347, 22 III/IV 4319, 22/10 V 46.]

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