53604
Nε-Trifluoroacetyl-L-lysine
≥96.0% (TLC)
Synonym(s):
ε-TFA-lysine
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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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Quality Level
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
Georgia Eleni Tsotsou et al.
Biochimie, 89(5), 591-604 (2007-02-13)
L-Lysine cyclodeaminase from Streptomyces pristinaespiralis was heterologously expressed in Escherichia coli, isolated to 90% purity after two purification steps and characterised. The size of the isolated recombinant enzyme was in agreement with the theoretical size calculated from the corresponding gene.
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Electrophoresis, 30(1), 36-49 (2008-12-25)
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