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63-91-2 - L-Phenylalanine, 99% - (S)-2-Amino-3-phenylpropionic acid - H-Phe-OH - A13238 - Alfa Aesar

A13238 L-Phenylalanine, 99%

Número CAS
63-91-2
Nombre Alternativo
(S)-2-Amino-3-phenylpropionic acid
H-Phe-OH

Tamaño Precio ($) Cantidad Disponibilidad
25g 23,70
50g 34,50
100g 59,40
500g 217,00
1000g 373,00
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L-Phenylalanine, 99%

MDL
MFCD00064227
EINECS
200-568-1

Propiedades químicas

Fórmula
C9H11NO2
Peso molecular
165.19
Punto de fusión
ca 275° dec.
Solubilidad
Soluble in water. Slightly soluble in methanol and ethanol. Insoluble in ethyl ether and benzene.

Aplicaciones

L-Phenylalanine is an aromatic organic compound containing amine and acid as functional groups. It is an essential amino acid and its structure can be considered as the derivative of 3-phenylpropionic acid, in which one hydrogen atom present at C-2 position is substituted with amino group. It is a chiral compound and consists of two optical isomers. It is also known as 2-amino-3-phenylpropanoic acid, beta-phenylalanine, L-alfa-amino-beta-phenylpropionic acid, H-Phe-OH and (S)-2-amino-3-phenylpropionic acid.

Notas

Incompatible with strong oxidizing agents.

Referencias documentales

Other amino acids have been resolved by crystallization of their complexes with L-phenylalanine, and decomplexation with activated carbon: Chem. Lett., 113 (1984).

Formation of the N,N-dibenzyl benzyl ester by reaction with benzyl bromide and base, followed by LAH reduction and Swern oxidation, lead to the N,N-dibenzyl (S)-ɑ-amino aldehyde, a useful chiral intermediate: Org. Synth., 76, 110 (1998).

Hou, Y.; Hossain, G. S.; Li, J.; Shin, H. D.; Liu, L.; Du, G. Production of phenylpyruvic acid from L-phenylalanine using an L-amino acid deaminase from Proteus mirabilis: comparison of enzymatic and whole-cell biotransformation approaches. Appl. Microbiol. Biotechnol. 2015, 99 (20), 8391-8402.

Liu, S. P.; Liu, R. X.; Xiao, M. R.; Zhang, L.; Ding, Z. Y.; Gu, Z. H.; Shi, G. Y. A systems level engineered E. coli capable of efficiently producing L-phenylalanine. Process Biochem. 2014, 49 (5), 751-757.

Otras referencias

Merck
14,7271
Beilstein
1910408
Código de tarifa arancelaria unificado
2922.49
TSCA
Yes
RTECS
AY7535000

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