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146982-27-6

146982-27-6 structure
146982-27-6 structure

Name Fmoc-Lys(Alloc)-OH
Synonyms Fmoc-Lys(Aloc)-OH
(S)-2-((((9H-fFuoren-9-yl)methoxy)carbonyl)amino)-6-(((allyloxy)carbonyl)amino)hexanoic acid
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-(prop-2-enoxycarbonylamino)hexanoic acid
N-[(Allyloxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine
MFCD00190872
L-Lysine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-[(2-propen-1-yloxy)carbonyl]-
Description Fmoc-Lys(Alloc)-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.

Density 1.2±0.1 g/cm3
Boiling Point 689.7±55.0 °C at 760 mmHg
Melting Point 87-91ºC
Molecular Formula C25H28N2O6
Molecular Weight 452.500
Flash Point 370.9±31.5 °C
Exact Mass 452.194733
PSA 113.96000
LogP 4.57
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.579
Storage condition 2-8°C
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 3
HS Code 2924299090

~95%

146982-27-6 structure

146982-27-6

Literature: Klar, Ulrich; Willuda, Joerg; Menrad, Andreas; Bosslet, Klaus Patent: US2005/234247 A1, 2005 ; Location in patent: Page/Page column 15 ;
Precursor  2

DownStream  1

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%