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13139-16-7

13139-16-7 structure
13139-16-7 structure

Name BOC-L-Isoleucine
Synonyms EINECS 236-074-8
(2S,3S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
N-(tert-Butoxycarbonyl)-L-isoleucine,Boc-L-isoleucine
(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-methylpentanoic acid
MFCD00038324
(2S,3S)-3-Methyl-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)pentanoic acid
Boc-L-Isoleucine
Boc-Ile-OH Hemihydrate
N-Boc-L-isoleucine Hemihydrate
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-isoleucine
N-(tert-Butoxycarbonyl)-L-isoleucine HeMihydrate
N-(tert-Butoxycarbonyl)-L-isoleucine
L-Isoleucine, N-[(1,1-dimethylethoxy)carbonyl]-
Description Boc-L-Ile-OH is an isoleucine 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 356.0±25.0 °C at 760 mmHg
Melting Point 66-69 °C(lit.)
Molecular Formula C11H21NO4
Molecular Weight 231.289
Flash Point 169.1±23.2 °C
Exact Mass 231.147064
PSA 75.63000
LogP 2.51
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.461
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases S24/25
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%