Name | N(α)-t-butoxycarbonyl-L-leucine |
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Synonyms |
N-Boc-L-leucine hydrate
(E)-N-{Hydroxy[(2-methyl-2-propanyl)oxy]methylene}-L-leucine (S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid MFCD00066067 L-LEUCINE-N-T-BOC:H2O L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]- BOC-LEU boc-leu-oh.h20 EINECS 236-073-2 N-tert-butoxycarbonyl-L-leucine BOC-L-LEUCINE-OH N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-leucine N-tert-butyloxycarbonyl-L-leucine BOC-L-Leucine N(alpha)-t-butoxycarbonyl-L-leucine Boc-Leu-OH,H2O Boc-Leu-OH.H2O N-Boc-L-leucine Monohydrate L-Leucine, N-[(1,1-dimethylethoxy)hydroxymethylene]-, (E)- BOC-L-LEU-OH BOC-LEU-OH N-(tert-Butoxycarbonyl)-L-leucine Monohydrate Boc-Leu-OH Monohydrate N-Boc-L-leucine |
Description | Boc-L-Leu-OH is a leucine derivative[1]. |
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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 |
Density | 1.1±0.1 g/cm3 |
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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 |
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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 |
Precursor 8 | |
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DownStream 10 | |
HS Code | 2924199090 |
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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% |