L-Phenylglycinol

Chemical properties

white to light yellow crystal powder

The Uses of L-Phenylglycinol

Enantiomer of L-Phenylalaninol, an inhibitor of intestinal Phenylalanine absorption.

The Uses of L-Phenylglycinol

Inhibits the intestinal absorption of Phenylalanine, making it a prospective treatment for phenylketonuria.

The Uses of L-Phenylglycinol

antiulcer

What are the applications of Application

L-Phenylalaninol is a reagent that reduces the secretion of gastric acid and prevents ulcer formation

Definition

ChEBI: L-phenylalaninol is an amino alcohol resulting from the formal reduction of the carboxy group of L-phenylalanine to the corresponding alcohol. It is a member of amphetamines, an amino alcohol, a primary amino compound and a primary alcohol.

General Description

(S)-(-)-2-Amino-3-phenyl-1-propanol is a chiral amino alcohol.

Purification Methods

It can be recrystallised from Et2O, *C6H6/pet ether (b 40-60o) or toluene and distilled in a vacuum. It has been purified by dissolving in Et2O, drying over K2CO3, filtering, evaporating to a small volume, cooling in ice and collecting the plates. Store them in the presence of KOH (i.e. CO2—free atm). [Karrer & Ehrhardt Helv Chim Acta 34 3203 1951, Oeda Bull Chem Soc Jpn 13 465 1938.] The picrate has m 141-141.5o (from EtOH/pet ether). The hydrogen oxalate has m 177o, 161-162o [Hunt & McHale J Chem Soc 2073 1957]. The racemate has m 87-88o from *C6H6/pet ether (75-77o from Et2O), and the hydrochloride has m 139-141o [Fodor et al. J Chem Soc 1858 1951]. [Beilstein 13 IV 1920.]