53604
Nε-Trifluoroacetyl-L-lysine
≥96.0% (TLC)
Synonym(s):
ε-TFA-lysine
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5 G
880,00 kr
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5 G
880,00 kr
About This Item
Empirical Formula (Hill Notation):
C8H13F3N2O3
CAS Number:
Molecular Weight:
242.20
Beilstein:
2122429
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
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Assay
≥96.0% (TLC)
form
powder
impurities
≤7% water
color
white to off-white
mp
>215 °C
solubility
2 M HCl: 10 mg/mL, clear, colorless
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
N[C@@H](CCCCNC(=O)C(F)(F)F)C(O)=O
InChI
1S/C8H13F3N2O3/c9-8(10,11)7(16)13-4-2-1-3-5(12)6(14)15/h5H,1-4,12H2,(H,13,16)(H,14,15)/t5-/m0/s1
InChI key
PZZHRSVBHRVIMI-YFKPBYRVSA-N
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Biochem/physiol Actions
Nε-Trifluoroacetyl-L-lysine is an inhibitor of L-lysine cyclodeaminase.
Nε-Trifluoroacetyl-L-lysine may be used to create synthetic organic polypeptides useful for nonaqueous capillary electrophoresis (NACE).
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Hervé Cottet et al.
Analytical chemistry, 75(20), 5554-5560 (2004-01-09)
Poly(Nepsilon-trifluoroacetyl-L-lysine) was used as a model solute to investigate the potential of nonaqueous capillary electrophoresis (NACE) for the characterization of synthetic organic polymers. The information obtained by NACE was compared to that derived from size exclusion chromatography (SEC) experiments, and
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The interaction of PEGylated poly(amino acid)s with their biological targets depends on their chemical nature and spatial arrangement of their building blocks. The synthesis, self-assembly, and DNA complexation of ABC terblock copolymers consisting of poly(ethylene glycol), (PEG), poly(l-lysine), and poly(l-leucine)
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