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About This Item
Empirical Formula (Hill Notation):
C8H13F3N2O3
CAS Number:
Molecular Weight:
242.20
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2122429
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
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
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
Min He et al.
Gene, 377, 109-118 (2006-06-30)
Meridamycin is a non-immunosuppressive, FKBP12-binding natural macrolide with potential therapeutic applications in a variety of medical conditions. To set the stage for structural modification of meridamycin by genetic engineering, we have cloned and completely sequenced approximately 117 kb of DNA
Determination of synthetic polypeptide conformations and molecular geometrical parameters by nonaqueous CE.
Plasson R, Vayaboury W, Giani O, Cottet H.
Electroanalysis, 28, 3617-3624 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 53604-25G-F | 04061832463827 |
| 53604-5G-F | 04061832463834 |