53604
Nε-Trifluoroacetyl-L-lysine
≥96.0% (TLC)
Sinonimo/i:
ε-TFA-lysine
Autenticati per visualizzare i prezzi organizzativi e contrattuali.
Informazioni su questo articolo
Formula empirica (notazione di Hill):
C8H13F3N2O3
Numero CAS:
Peso molecolare:
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).
Classe di stoccaggio
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
Qixian Chen et al.
ACS applied materials & interfaces, 8(37), 24404-24414 (2016-09-01)
Nucleic acid-based therapy has emerged as a revolutionary methodology for treatment of the diseases related to protein dysfunction; however, lack of systemically applicable synthetic delivery systems limits its current usage in local applications, particularly for DNA-based therapy with regard to
David Ulkoski et al.
Macromolecular bioscience, 18(8), e1800108-e1800108 (2018-06-14)
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)
Numero articolo commerciale globale
| SKU | GTIN |
|---|---|
| 53604-25G-F | 04061832463827 |
| 53604-5G-F | 04061832463834 |