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53604

Sigma-Aldrich

Nε-Trifluoroacetyl-L-lysine

≥96.0% (TLC)

Sinonimo/i:

ε-TFA-lysine

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About This Item

Formula empirica (notazione di Hill):
C8H13F3N2O3
Numero CAS:
10009-20-8
Peso molecolare:
242.20
Beilstein:
2122429
Numero MDL:
MFCD00037223
Codice UNSPSC:
12352209
ID PubChem:
57651423
NACRES:
NA.26

Livello qualitativo

100

Saggio

≥96.0% (TLC)

Stato

powder

Impurezze

≤7% water

Colore

white to off-white

Punto di fusione

>215 °C

Solubilità

2 M HCl: 10 mg/mL, clear, colorless

applicazioni

peptide synthesis

Temperatura di conservazione

2-8°C

Stringa SMILE

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
PZZHRSVBHRVIMI-YFKPBYRVSA-N

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Categorie correlate

Azioni biochim/fisiol

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).

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCBQ5965V
BCBK8041V
BCBJ3157V
BCBG9541V
BCBF8285V

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L-tirosina reagent grade, ≥98% (HPLC)

Sigma-Aldrich

T3754

L-tirosina

Piperidina ReagentPlus®, 99%

Sigma-Aldrich

104094

Piperidina

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.
Gerhard K E Scriba
Journal of chromatography. A, 1159(1-2), 28-41 (2007-02-24)
Nonaqueous background electrolytes broaden the application of capillary electrophoresis displaying altered separation selectivity and interactions between analytes and buffer additives compared to aqueous background electrolytes. In addition, nonaqueous capillary electrophoresis (NACE) appears to be ideally suited for online coupling with
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
Laurent Geiser et al.
Electrophoresis, 30(1), 36-49 (2008-12-25)
This review article presents recent developments and applications of non-aqueous capillary electrophoresis (NACE): The text covers the period from the previous review (L. Geiser, J. L. Veuthey, Electrophoresis 2007, 28, 45-57) to summer 2008. We focus primarily on the analysis
S M Furst et al.
International archives of allergy and immunology, 114(1), 46-53 (1997-09-26)
The purpose of this study was to investigate lymphocyte adhesion to Kupffer cells as a component of an immune-mediated mechanism for halothane hepatitis. Kupffer cells were isolated from guinea pigs exposed to 1.0% halothane/40% oxygen and cultured with various synthetic
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