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H-Phe-OEt.HCl

Names

[ CAS No. ]:
3182-93-2

[ Name ]:
H-Phe-OEt.HCl

[Synonym ]:
Ethyl L-phenylalaninate hydrochloride (1:1)
L-Phenylalanine, ethyl ester, hydrochloride (1:1)
L-Phenylalanine Ethyl Ester Hydrochloride
PHENYLALANINE-OET HCL
D,L-phenylalanine ethyl ester hydrochloride
H-Phe-OEt.HCl
L-Phe-OEt.HCL
Ethyl L-phenylalanin
H-L-Phe-OEt*HCl
L-Phe-OEt hydrochloride
Ethyl L-Phenylalaninate Hydrochloride
L-phenylalanine ethylester
Phe-OEt HCl
L-PHENYLALANINE ETHYL ESTER HCL
EINECS 221-673-9
L-PHANYLALANINEETHYLESTERHCL
MFCD00012507
ethyl L-phenylalanine hydrochloride

Biological Activity

[Description]:

Ethyl L-phenylalaninate hydrochloride is a phenylalanine derivative[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-942.

Chemical & Physical Properties

[ Boiling Point ]:
281.3ºC at 760mmHg

[ Melting Point ]:
155-156 °C(lit.)

[ Molecular Formula ]:
C11H16ClNO2

[ Molecular Weight ]:
229.703

[ Flash Point ]:
140.3ºC

[ Exact Mass ]:
229.086960

[ PSA ]:
52.32000

[ LogP ]:
2.62180

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29224995

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 29224995

Articles

Optimisation of a system for the co-translational incorporation of a keto amino acid and its application to a tumour-specific Anticalin.

Protein Eng. Des. Sel. 28 , 553-65, (2015)

The bioorthogonal keto group has attracted interest for the site-specific chemical conjugation of recombinant proteins under mild conditions, e.g. with aminooxy-functionalised fluorescent probes, radi...


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Related Compounds