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Merck
CN

A4251

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
PubChem Substance ID:
UNSPSC Code:
12352200
NACRES:
NA.26
EC Number:
219-108-6
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InChI key

YIVZYFDBEPMPNL-UHFFFAOYSA-N

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)

SMILES string

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

assay

≥98% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

color

white

storage temp.

2-8°C

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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M T Hearn et al.
Analytical chemistry, 71(21), 4874-4885 (1999-11-24)
In this paper, we describe a general procedure to evaluate the thermodynamics of the interaction between polypeptides and hydrophobic ligands in the presence of aquo-organic solvent mixtures. These studies address experimental requirements for the determination of the linear free energy
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
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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