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 |
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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 |
TRYPTAMINE HYDROCHLORIDE
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