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246557

Sigma-Aldrich

Tryptamine hydrochloride

99%

Sinônimo(s):

2-(3-Indolyl)ethylamine hydrochloride, 3-(2-Aminoethyl)indole hydrochloride

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About This Item

Fórmula empírica (Notação de Hill):
C10H12N2 · HCl
Número CAS:
343-94-2
Peso molecular:
196.68
Beilstein:
3568419
Número CE:
206-446-4
Número MDL:
MFCD00012682
Código UNSPSC:
12352100
ID de substância PubChem:
24278134
NACRES:
NA.22

Nível de qualidade

200

Ensaio

99%

forma

powder

pf

253-255 °C (lit.)

solubilidade

water: soluble 0.1 g/10 mL, clear to slightly hazy, colorless to yellow

cadeia de caracteres SMILES

Cl[H].NCCc1c[nH]c2ccccc12

InChI

1S/C10H12N2.ClH/c11-6-5-8-7-12-10-4-2-1-3-9(8)10;/h1-4,7,12H,5-6,11H2;1H

chave InChI

KDFBGNBTTMPNIG-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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

Ações bioquímicas/fisiológicas

Vasoactive; may have a neuromodulator function.

Outras notas

Biogenic amine formed from the decarboxylation of tryptophan by L-aromatic amino acid decarboxylase.

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H317,H318

Classificações de perigo

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1A

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
MKCK1360
MKBZ1617V
MKBH7797V
MKBC2907V
MKBC2907

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Photochemistry and photobiology, 73(2), 97-104 (2001-03-29)
The fluorescence properties of 3-methylindole (MI), 3-indoleacetic acid (IAA), 3-indoleethyltrimethylammonium bromide (IETA), L-tryptophan (Trp) and tryptamine hydrochloride (TA) were studied in reverse micelles solutions made with the cationic surfactant benzylhexadecyldimethylammonium chloride (BHDC) in benzene as a function of the molar
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