Boc-D-Leu-OH.H2O

Names

[ Name ]:
Boc-D-Leu-OH.H2O

[Synonym ]:
MFCD00038294
BOC-D-Leucinemonohydrate
Boc-D-Leu-OH&BOC-D-LEU
N-BOC-D-Leucine.H2O
Boc-D-Leu-OH Hydrate
N-(tert-Butoxycarbonyl)-D-leucine
D-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-, hydrate (1:1)
BOC-D-LEUCINE-OH
N-T-BOC-D-LEUCINE
Boc-D-Leu-OH
N-(tert-Butoxycarbonyl)-D-leucine hydrate (1:1)
N-(tert-Butoxycarbonyl)-D-leucine Hydrate
BOC-D-LEU-OH2O
N-tert-butoxycarbonyl-D-leucine
n-boc-d-leucine
N-Boc-D-leucine Hydrate
D-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-
tert-butoxycarbonyl-D-leucine
N-(t-butyloxycarbonyl)-D-leucine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine hydrate (1:1)
Boc-D-Leu-OH.H2O
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine
BOC-D-LEUCINE
Boc-(R)-leucine

Biological Activity

[Description]:

(tert-Butoxycarbonyl)-D-leucine 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]:
1.1±0.1 g/cm3

[ Boiling Point ]:
356.0±25.0 °C at 760 mmHg

[ Melting Point ]:
85-87ºC(lit.)

[ Molecular Formula ]:
C₁₁H₂₁NO₄

[ Molecular Weight ]:
231.289

[ Flash Point ]:
169.1±23.2 °C

[ Exact Mass ]:
231.147064

[ PSA ]:
84.86000

[ LogP ]:
2.51

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

[ Index of Refraction ]:
1.461

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

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%

Articles

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...