L-Phenylglycinol
CAS No.
3182-95-4
Chemical Name:
L-Phenylglycinol
Synonyms
L-PHE-OL;H-PHE-OL;H-L-PHE-OL;l-1-propano;L-PHENYLANINOL;L璓henylalaninol;L-PHENYLALAINOL;5-PHENYLALANINOL;L-Phenylglycinol;L-PHENYLALANINOL
CBNumber:
CB6460985
Molecular Formula:
C9H13NO
Formula Weight:
151.21
MOL File:
3182-95-4.mol
L-Phenylglycinol Properties
Melting point:
92-94 °C(lit.)
alpha
-23 º (c=5,EtOH)
Boiling point:
273.23°C (rough estimate)
Density
1.0406 (rough estimate)
refractive index
-24.5 ° (C=5, EtOH)
storage temp.
-15°C
solubility
Soluble in chloroform, ethyl acetate, ethanol and methanol.
pka
12.85±0.10(Predicted)
form
Crystalline Powder
color
White to light yellow
optical activity
[α]22/D 22.8°, c = 1.2 in 1 M HCl
Sensitive
Air Sensitive
BRN
2208238
InChIKey
STVVMTBJNDTZBF-VIFPVBQESA-N
CAS DataBase Reference
3182-95-4(CAS DataBase Reference)
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Risk and Safety Statements
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Product description
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Sigma-Aldrich
190438
(S)-(?)-2-Amino-3-phenyl-1-propanol
98%, optical purity ee: 99% (HPLC)
3182-95-4
1g
$33.9
2020-08-18
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Sigma-Aldrich
190438
(S)-(?)-2-Amino-3-phenyl-1-propanol
98%, optical purity ee: 99% (HPLC)
3182-95-4
10g
$237
2020-08-18
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TCI Chemical
P1028
L-Phenylalaninol >98.0%(GC)(T)
3182-95-4
5g
$82
2020-06-24
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TCI Chemical
P1028
L-Phenylalaninol >98.0%(GC)(T)
3182-95-4
25g
$274
2020-06-24
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Alfa Aesar
A11586
L-Phenylalaninol, 98%
3182-95-4
25g
$306
2020-06-24
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L-Phenylglycinol Chemical Properties,Uses,Production
Chemical Properties
white to light yellow crystal powder
Uses
Enantiomer of L-Phenylalaninol, an inhibitor of intestinal Phenylalanine absorption.
Uses
Inhibits the intestinal absorption of Phenylalanine, making it a prospective treatment for phenylketonuria.
Uses
antiulcer
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.]
L-Phenylglycinol Preparation Products And Raw materials
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Global 454
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L-Phenylglycinol Spectrum
3182-95-4(L-Phenylglycinol)Related Search:
((1S)-1-HydroxyMethyl-2-phenylethyl)aMine
(2S)-2-AMino-3-phenyl-1-propanol
(S)-(-)-2-AMino-3-phenyl-1-glycinol
(S)-2-AMino-1-hydroxy-3-phenylpropane
(βS)-β-AMino-benzenepropanol
(S)-(-)-2-AMINO-3-PHENYL-1-PROPANOL FOR
(S)-3-Phenyl-2-aMino-1-propanol
1-Propanol, 2-aMino-3-phenyl-, L- (8CI)
(2S)-2-amino-3-phenylpropan-1-ol
(S)-(-)-2-Amino-3-phenyl-1-propanol~H-Phe-ol
(S)-(-)-2-Amino-3-phenyl-1-propanol 98%, optical purity ee: 99% (HPLC)
L-Phenylalaninol≥ 99% (Chiral Purity)
L-2-Amino-3-phenyl-1-propanol,99%e.e.
(S)-2-AMINO-3-PHENYL-1-PROPANOL
(S)-2-AMINO-3-PHENYL-PROPAN-1-OL
(S)-(-)-2-AMINO-3-PHENYL-PROPANOL
(S)-(-)-PHENYLALANINOL
(S)-PHENYLALANINOL
L璓henylalaninol
(S)-(-)-2-Amino-3-phenyl-propanolL-Phenylalaninol
L-Phenylalaninol, 98%+
Benzenepropanol, .beta.-amino-, (.beta.S)-
L-PHENYLALAINOL
5-PHENYLALANINOL
(L)-(-)-2-PHENYLALANINOL / L-(-)-2-AMINO-3-PHENYL-1-PROPANOL
L-PHENYLANINOL
L-Phenylglycinol
L(-)-2-AMINO-3-PHENYL-1-PROPANOL
L-2-amino-3-phenylpropan-1-ol
L-2-PHENYLALANINOL
L-PHE-OL
(-)-L-PHENYLALANINOL
L(-)-PHENYLALANINOL
L-PHENYLALANINOL
L-(S)-PHENYLALANINOL
L-BENZYLGLYCINOL
H-L-PHE-OL
H-PHENYLALANINOL
H-PHE-OL
BENZENEPROPANOL, B-AMINO-, (BS)-
1-PHENYLALANINOL
(S)-(-)-2-AMINO-3-PHENYL-1-PROPANOL
(S)-(-)-2-amino-3-phenyl-1-propanol (L-phenylalaninol)
L(-)-2-Amino-3-phenyl-1-propano
Benzenepropanol, beta-amino-, (S)-
3-Phenyl-2-amino-1-propanol
β-Aminobenzene-1-propanol
L(-)-2-Amino-3-phenyl-1-propanol,98%
(s)-2-benzylethanolamine
(s)-benzenepropano
-2-Amino-3-phenyl-1-propanol
l-1-propano
L-Phenylalaninol>
3182-95-4
C6H5CH2CHNH2CH2OH
Amino Alcohols (Chiral)
Asymmetric Synthesis
Organic Building Blocks