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L-Tyrosine Ethyl Ester Hydrochloride

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L-Tyrosine Ethyl Ester Hydrochloride Basic information

Product Name:
L-Tyrosine Ethyl Ester Hydrochloride
Synonyms:
  • (S)-2-AMINO-3-(4-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER HCL
  • TEE
  • ethylester,hydrochloride,l-tyrosin
  • tyrosineethylesterhydrochloride
  • TYROSINE-OET HCL
  • Tyr-Oet Hcl
  • L-TYROSINE ETHYL ESTER MONOHYDROCHLORIDE
  • L-TYROSINE ETHYL ESTER HYDROCHLORIDE SALT
CAS:
4089-07-0
MF:
C11H16ClNO3
MW:
245.7
EINECS:
223-820-2
Product Categories:
  • Amino Acids
  • I - ZPeptide Synthesis
  • Tyrosine [Tyr, Y]
  • Amino Acids and Derivatives
  • Amino Acid Derivatives
  • Modified Amino Acids
  • Amino Acids
  • Amino Acid Ethyl Esters
  • Amino Acids (C-Protected)
  • Biochemistry
  • Amino hydrochloride
  • Peptide Synthesis
  • Tyrosine
Mol File:
4089-07-0.mol
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L-Tyrosine Ethyl Ester Hydrochloride Chemical Properties

Melting point:
166-170 °C
alpha 
[α]D20 +26~+30° (c=5, C2H5OH)
refractive index 
-6.5 ° (C=2, H2O)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
powder to crystal
color 
White to Almost white
Water Solubility 
Soluble in water (3.685e+005 mg/L @ 25°C (est.)).
BRN 
4725904
InChIKey
BQULAXAVRFIAHN-PPHPATTJSA-N
LogP
1.060 (est)
CAS DataBase Reference
4089-07-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-37/39-26
WGK Germany 
2
RTECS 
YP2580000
HS Code 
29225090

MSDS

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L-Tyrosine Ethyl Ester Hydrochloride Usage And Synthesis

Chemical Properties

White to off-white microcrystalline powder

Uses

L-Tyrosine Ethyl Ester Hydrochloride is used as a medical and organic intermediate and as an important amino protective agent. It is also used to introduce t-Boc protect gene.

Application

Papain is also used for synthesizing poly(L-tyrosine) and poly(L-glutamic acid) using L-tyrosine ethyl ester hydrochloride and L-glutamic acid diethyl ester hydrochloride as the substrates, respectively. The protease-catalyzed copolymerization of amino acids is first achieved by papain using L-glutamic acid ester and various amino acid esters as substrates.
A mixture of L-tyrosine ethyl ester hydrochloride, the appropriate acid anhydri-des, triethylamine and dry tetrahydrofuran, was warmed for an hour in an atmosphere of nitrogen. After removing the amine salt, Ic and Id became crystalline on standing overnight in the cold.

Preparation

synthesis of L-Tyrosine Ethyl Ester Hydrochloride: Esterification of 25 g. ol L-tyrosine (0.014 mole) with ethanolic hydrogen chloride gave 24.1 g. of L-tyrosine ethyl ester hydrochloride (80%). Liberation of the ester by slurrying the hydrochloride in chloroform rollowed by the addition of chloroform saturated with ammonia, removal of the ammonium chloride by filtration and evaporation of the chloroform gave 19.4 g. of L-tyrosine ethyl ester (67%), m.p. 106-108 ° .

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