Boc-Leu-OH.H2O

Modify Date: 2024-01-02 18:30:48

Boc-Leu-OH.H2O Structure
Boc-Leu-OH.H2O structure
Common Name Boc-Leu-OH.H2O
CAS Number 13139-15-6 Molecular Weight 231.289
Density 1.1±0.1 g/cm3 Boiling Point 339.7±44.0 °C at 760 mmHg
Molecular Formula C11H21NO4 Melting Point 85-87 °C
MSDS Chinese USA Flash Point 159.2±28.4 °C

 Use of Boc-Leu-OH.H2O


Boc-L-Leu-OH is a leucine derivative[1].

 Names

Name N(α)-t-butoxycarbonyl-L-leucine
Synonym More Synonyms

 Boc-Leu-OH.H2O Biological Activity

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.

 Chemical & Physical Properties

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

 Safety Information

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

 Synthetic Route

 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%

 Articles3

More 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...

In situ fabrication of cleavable peptide arrays on polydimethylsiloxane and applications for kinase activity assays.

Anal. Chim. Acta 865 , 53-9, (2015)

Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with ...

Concise synthesis of PM-94128 and Y-05460M-A.

J. Org. Chem. 74(19) , 7566-9, (2009)

The enantioselective total synthesis of PM-94128, a potent cytotoxin of microbial origin, was accomplished by a concise nine-step sequence of reactions in 14% overall yield from N-Boc-l-leucine. The s...

 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
Top Suppliers:I want be here





Get all suppliers and price by the below link:

Boc-Leu-OH.H2O suppliers


Price: ¥180/100g

Reference only. check more Boc-Leu-OH.H2O price