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Ethyl L-tyrosinate

Names

[ CAS No. ]:
949-67-7

[ Name ]:
Ethyl L-tyrosinate

[Synonym ]:
QR D1YZVO2 &&L or S Form
H-TYR-OET
EINECS 213-442-6
L-Tyrosine ethyl
L-Tyr-OEtHC
MFCD00063046
Ethyl L-tyrosinate
EthylL-tyrosinate
ethyl tyrosinate
TYROSINE ETHYL ESTER
TYROSINE-OET
L-Tyrosine, ethyl ester
Tyrosine, ethyl ester, L-
L-Tyr-OEt
L-Tyrosine Ethyl Ester
ethyl tyrosine ester

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
343.3±27.0 °C at 760 mmHg

[ Melting Point ]:
103 °C

[ Molecular Formula ]:
C11H15NO3

[ Molecular Weight ]:
209.242

[ Flash Point ]:
161.4±23.7 °C

[ Exact Mass ]:
209.105194

[ PSA ]:
72.55000

[ LogP ]:
1.06

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.553

[ Storage condition ]:
−20°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922509090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Mechanism of papain-catalyzed synthesis of oligo-tyrosine peptides.

Enzyme Microb. Technol. 75-76 , 10-7, (2015)

Di-, tri-, and tetra-tyrosine peptides with angiotensin I-converting enzyme inhibitory activity were synthesized by papain-catalyzed polymerization of L-tyrosine ethyl ester in aqueous media at 30 °C....

Evaluation of Pseudotrypsin Cleavage Specificity Towards Proteins by MALDI-TOF Mass Spectrometry.

Protein Pept. Lett. 22 , 1123-32, (2015)

Trypsin is a protease, which is commonly used for the digestion of protein samples in proteomic experiments. The process of trypsin autolysis is known to produce autolytic peptides as well as active e...

Transverse dephasing optimised NMR spectroscopy in solids: natural-abundance 13C correlation spectra.

ChemPhysChem 5(6) , 869-75, (2004)


More Articles


Related Compounds