N-Boc-L-Norleucine

Names

[ Name ]:
N-Boc-L-Norleucine

[Synonym ]:
MFCD00037270
N-(tert-Butoxycarbonyl)-L-norleucine
L-Norleucine, N-[(1,1-dimethylethoxy)carbonyl]-
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-norleucine
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
Boc-Nle-OH
N-(tert-Butoxycarbonyl)norleucine

Biological Activity

[Description]:

Boc-Nle-OH is a leucine derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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]:
1.063±0.06 g/cm3

[ Boiling Point ]:
362.1±25.0 °C at 760 mmHg

[ Molecular Formula ]:
C₁₁H₂₁NO₄

[ Molecular Weight ]:
231.289

[ Flash Point ]:
172.8±23.2 °C

[ Exact Mass ]:
231.147064

[ PSA ]:
75.63000

[ LogP ]:
2.69

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.463

[ Storage condition ]:
-15°C

[ Water Solubility ]:
Slightly soluble (1.5 g/L) (25 ºC)

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

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%