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13139-15-6

13139-15-6 structure
13139-15-6 structure

Name N(α)-t-butoxycarbonyl-L-leucine
Synonyms N-Boc-L-leucine hydrate
Tert butoxycbonyl-l-leucine monohydrate
N-Cboxy-L-leucine N-tert-Butyl Ester
MFCD00066067
BOC-L-LEUCINE
BOC-LEU-OH·H2O
L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]
Boc-L-Leu-OHH20
N(α)-t-butoxycbonyl-L-leucine
BOC-L-LEUCINE-OH
N-tert-butyloxycarbonyl-L-leucine
N-TERT-BUTOXYCBONYL-L-LEUCINE
L-Leucine-2-13C15N-N-t-BOCH2O
eucine, N-((1,1-dimethyL
n-[(1,1-dimethylethoxy)carbonyl]-l-leucin
(S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid
Boc-Leu-OH hydrate Hydrate
N-t-BOC-Leucine
BOC-LEU
Boc-Leu-OH · H2O
BOC-L-Leucine Monohydrate extrapure
N-tert-butoxycarbonyl-L-leucine
Boc-Leu-OH >= (HPLC)
BOC-L-Leucine
N(alpha)-t-butoxycarbonyl-L-leucine
Boc-Leu-OH,H2O
N-ALPHA-T-BOC-L-LEUCINE
L-Leucine-2-13C15N-N-t-BOC2O
4-methyl-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanoate
N-(tert-Butoxycbonyl)-L-leucine Monohydrate>
"L-Leucine-15N, N-Boc, Monohydrate"
N-Cboxy Ester
L-Leucine-1-13C-N-t-BOC
L-LEUCINE-N-T-BOC:H2O
(S)-2-(tert-Butoxycbonylamino)-4-methylvaleric acid
(S)-Boc-2-amino-4-methylpentanoic acid hydrate
Boc-Leu-OH·H
N-ALPHA-T-BUTYLOXYCBONYL-L-LEUCINE MONOHYDRATE
Boc-L-leucine hydrate (HPLC)
EINECS 236-073-2
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-leucine
Butoxycbonyl-L-leucine
BOC-L-LEU-OH
N-(tert-Butoxycbonyl)-L-leucine
L-LEUCINE, N-BOC PROTECTED
Boc-Leu-OH Monohydrate, >=
n-tert-boc-leucine
N-Boc-L-leucine Monohydrate,e.e
N-[(1,1-dimethylethoxy)carbonyl]-L-leucine
(2S)-2-(tert-Butoxycbonylamino)-4-methylpentanoic acid
N-Boc-L-leucine Boc-Leu-OH
(E)-N-{Hydroxy[(2-methyl-2-propanyl)oxy]methylene}-L-leucine
BOC-L-Leucine //BP
boc-leu-oh.h20
BOC-L-LEU-OH MONOHYDRATE
Bok - L - leucine
Boc-L-Leu.H2O
N-(tert-butyloxycbonyl)-L-leucine
BOC-L-Leu
N-Boc-L-leucine Monohydrate
N-tert-Butoxycbonyl-L-leucine·H2O
N(alpha)-t-butoxycbonyl-L-leucine
BOC-LEU-OH
(S)-2-(tert-butyloxycbonylamino)-4-methylvaleric acid
N-(tert-Butoxycarbonyl)-L-leucine Monohydrate
Boc-Leu-OH Monohydrate
N-[(1,1-DiMethylethoxy)carbonyl]leucine
Boc-Leu-OH
N-Boc-L-leucine
Description Boc-L-Leu-OH is a leucine 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 1.1±0.1 g/cm3
Boiling Point 339.7±44.0 °C at 760 mmHg
Melting Point 85-87 °C
Molecular Formula C11H21NO4
Molecular Weight 231.289
Flash Point 159.2±28.4 °C
Exact Mass 231.147064
PSA 75.63000
LogP 2.99
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.472
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi,Xn
Risk Phrases R20/21/22
Safety Phrases 26-36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090
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%
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