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Key Documents

A4251

Sigma-Aldrich

N-Acetyl-L-phenylalanine ethyl ester

Synonym(s):

N-Ac-l-Phe-Oet, APAEE

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About This Item

Empirical Formula (Hill Notation):
C13H17NO3
CAS Number:
Molecular Weight:
235.28
EC Number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.26

Assay

≥98% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

color

white

storage temp.

2-8°C

SMILES string

CCOC(=O)C(Cc1ccccc1)NC(C)=O

InChI

1S/C13H17NO3/c1-3-17-13(16)12(14-10(2)15)9-11-7-5-4-6-8-11/h4-8,12H,3,9H2,1-2H3,(H,14,15)

InChI key

YIVZYFDBEPMPNL-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Ritu Sareen et al.
Applied microbiology and biotechnology, 79(3), 399-405 (2008-04-23)
A protease was purified from the cell-free supernatant of Bacillus licheniformis RSP-09-37, a mutant from a thermophilic bacterial strain, B. licheniformis RSP-09, using affinity chromatography with alpha-casein agarose resin. The protease was purified 85-fold to electrophoretic homogeneity. The apparent molecular
Hua Zhao et al.
Biotechnology letters, 32(8), 1109-1116 (2010-04-07)
Three new ether-functionalized hydrophobic ionic liquids (ILs) were synthesized. Two proteases (subtilisin and alpha-chymotrypsin both covalently immobilized on chitosan) exhibited high synthetic activity (1-3 micromol/min x g) and selectivity (>97-99%, esterification over hydrolysis) in these ILs containing 10-15% (v/v) water
P C Quan et al.
Journal of immunology (Baltimore, Md. : 1950), 128(4), 1786-1791 (1982-04-01)
The mechanism of cytolysis by murine NK cells was analyzed using a variety of metabolic inhibitors that have proven informative in studying the lytic mechanism of CTL and the mechanism of histamine release by mast cells. Target cell binding occurred
Muhammad Nazir Tahir et al.
Bioprocess and biosystems engineering, 37(4), 687-695 (2013-08-28)
In this study, serine protease (subtilisin Carlsberg) was immobilized on pentynyl dextran (PyD, O-alkynyl ether of dextran, 1) and used for the transesterification of N-acetyl-L-phenylalanine ethyl ester (2) with different aliphatic (1-propanol, 1-butanol, 1-pentanol, 1-hexanol) and aromatic (benzyl alcohol, 2-phenyl
R L Levine et al.
Biochemistry, 21(11), 2600-2606 (1982-05-25)
The ultraviolet absorption spectrum of proteins in 6 M guanidine is approximately that of the sum of the spectra of the constituent aromatic amino acids, phenylalanine, tyrosine, and tryptophan, plus contributions from light scattering and disulfides. A multicomponent analysis of

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