H-Lys(Tfa)-OH

Modify Date: 2024-01-02 18:44:44

H-Lys(Tfa)-OH Structure
H-Lys(Tfa)-OH structure
 Common Name H-Lys(Tfa)-OH
CAS Number 10009-20-8 Molecular Weight 242.196
Density 1.3±0.1 g/cm3 Boiling Point 382.5±42.0 °C at 760 mmHg
Molecular Formula C8H13F3N2O3 Melting Point 258ºC
MSDS Chinese USA Flash Point 185.1±27.9 °C

 Use of H-Lys(Tfa)-OH


H-Lys(Tfa)-OH is a lysine derivative[1].

 Names

Name N6-trifluoroacetyl-L-lysine
Synonym More Synonyms

 H-Lys(Tfa)-OH Biological Activity

Description H-Lys(Tfa)-OH is a lysine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 382.5±42.0 °C at 760 mmHg
Melting Point 258ºC
Molecular Formula C8H13F3N2O3
Molecular Weight 242.196
Flash Point 185.1±27.9 °C
Exact Mass 242.087830
PSA 92.42000
LogP -0.22
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.444
Storage condition 2-8°C
Water Solubility 2 M HCl: 10 mg/mL, clear, colorless

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 1
HS Code 2924199090

 Customs

HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles7

More Articles
Non-aqueous capillary electrophoresis 2005-2008.

Electrophoresis 30 , 36-49, (2009)

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, Electr...

Nonaqueous capillary zone electrophoresis of synthetic organic polypeptides.

Anal. Chem. 75 , 5554-5560, (2003)

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. T...

Nonaqueous capillary electrophoresis-mass spectrometry.

J. Chromatogr. A. 1159 , 28-41, (2007)

Nonaqueous background electrolytes broaden the application of capillary electrophoresis displaying altered separation selectivity and interactions between analytes and buffer additives compared to aqu...

 Synonyms

L-Lysine, N6-(2,2,2-trifluoroacetyl)-
H-Lys(Tfa)-OH
(S)-2-Amino-6-pivalamidohexanoic acid
N6-(Triflu​oroacetyl)​-L-lysine
N-(Trifluoroacetyl)-L-lysine
Nepsilon-Trifluoroacetyl-L-lysine
Nepsilon-(Trifluoroacetyl)-L-lysine
N(6)-trifluoroacetyl-L-lysine
MFCD00037223
L-Lysine, N-(2,2,2-trifluoroacetyl)-
(2S)-2-amino-6-[(2,2,2-trifluoroacetyl)amino]hexanoic acid
QVYZ4MVXFFF &&L or S Form
Ne-Trifluoroacetyl-L-lysine
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