3-(2-aminoethyl)-5-fluoro-indolhydrochloride

3-(2-aminoethyl)-5-fluoro-indolhydrochloride - Names and Identifiers

Name	5-fluorotryptamine hcl
Synonyms	AKOS JY2082969 5-FLUOROTRYPTAMINE HCL 5-fluorotryptamine hcl 5-Fluorotryptamine hydrochloride 5-FLUOROTRYPTAMINE HYDROCHLORIDE 2-(5-fluoro-1H-indol-3-yl)ethanamine 3-(2-aminoethyl)-5-fluoro-indolhydrochloride 3-(2-AMINOETHYL)-5-FLUOROINDOLE HYDROCHLORIDE 2-(5-FLUORO-1H-INDOL-3-YL)ETHANAMINE HYDROCHLORIDE 2-(5-FLUORO-1H-INDOL-3-YL)ETHYLAMINE HYDROCHLORIDE 2-(5-FLUORO-1H-INDOL-3-YL)-1-ETHANAMINE HYDROCHLORIDE
CAS	2711-58-2
EINECS	220-307-5
InChI	InChI=1/C10H11FN2.Cl/c11-8-1-2-10-9(5-8)7(3-4-12)6-13-10;/h1-2,5-6,13H,3-4,12H2

3-(2-aminoethyl)-5-fluoro-indolhydrochloride - Physico-chemical Properties

Molecular Formula	C10H12ClFN2
Molar Mass	214.67
Melting Point	277-283
Appearance	Crystalline powder
Storage Condition	-20°C

3-(2-aminoethyl)-5-fluoro-indolhydrochloride - Risk and Safety

Hazard Symbols	Xi - Irritant
WGK Germany	3
RTECS	NL4055600
Hazard Class	IRRITANT

3-(2-aminoethyl)-5-fluoro-indolhydrochloride - Introduction

5-fluorotryptamine hcl(5-fluorotryptamine HCl) is an organic compound with the chemical formula C10H11FN2 • HCl.

This compound is an analog of tryptamine, in which one hydrogen atom is replaced by fluorine. It is in the form of white crystals or crystalline powder. 5-fluorotryptamine hcl is superior to its anhydrous form in solubility and stability. It is mainly used as a reagent in laboratory research.

5-fluorotryptamine hcl has been reported to have antidepressant, hypnotic and sedative activities. It is also used in neurochemical studies as an agonist and modulator of serotonin receptors.

The preparation method of 5-fluorotryptamine hcl is generally obtained by synthetic chemical reaction. The specific method includes reacting tryptamine with fluorine gas, and then reacting with hydrochloric acid to obtain hydrochloride.

Regarding safety information, 5-fluorotryptamine hcl is an organic compound with certain toxicity. It should be operated under suitable laboratory conditions and follow relevant safe operating procedures. Care should be taken to avoid contact with eyes, skin and mucous membranes, and appropriate protective gloves, glasses and laboratory coats should be worn when necessary. Before any use, the safety data sheet of the product should be read carefully and the relevant safety operation guidelines should be followed.

Last Update：2024-04-10 22:29:15