Free release

TRYPTAMINE HYDROCHLORIDE

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Name: TRYPTAMINE HYDROCHLORIDE
CAS: 61-54-1 ;343-94-2
Synonyms: TRYPTAMINE, 98+% ; 3-(2-AMINOETHYL)INDOLE HCL ; INDOLE-3-ETHYLAMINE HYDROCHLORIDE ; BETA-INDOLE-ETHYLAMINE HYDROCHLORIDE ; TRYPTAMINE HYDROCHLORIDE ; BETA-3-INDOLYLETHYLAMINE HYDROCHLORIDE ; 2-(3-INDOLYL)ETHYLAMINE HYDROCHLORIDE ; 2-(1H-INDOL-3-YL)ETHANAMINE HYDROCHLORIDE ; TRYPTAMINE (HCL) ; 3-(2-AMINOETHYL)INDOLE HYDROCHLORIDE
MDL.: MFCD00012682
H bond acceptor: 2
H bond donor: 2
Smile: c1ccc2c(c1)c(c[nH]2)CCN.Cl
InChi: 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
InChiKey: InChIKey=KDFBGNBTTMPNIG-UHFFFAOYSA-N

Property

Melting Point: 253-255 DEG C(LIT)/253-255 °C
Comments: APPLICATION: 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. BETA-CARBOLINIUM CATIONS AS NEW ANTIMALARIAL AGENTS
BIOCHEM/PHYSIOL ACTIONS: MAY HAVE A NEUROMODULATOR FUNCTION
BIOCHEM/PHYSIOL ACTIONS: VASOACTIVE
OTHER NOTES: BIOGENIC AMINE FORMED FROM THE DECARBOXYLATION OF TRYPTOPHAN BY L-AROMATIC AMINO ACID DECARBOXYLASE
RTECS: NL4375000
UNSPSC: 12352100
WGK: 3

Safety information

Safe Code: S:22,24/25
WGK Germany: 3

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