N-Boc-L-valine

Modify Date: 2024-01-10 21:50:02

N-Boc-L-valine Structure
N-Boc-L-valine structure
Common Name N-Boc-L-valine
CAS Number 54895-12-4 Molecular Weight 217.262
Density 1.1±0.1 g/cm3 Boiling Point 341.8±25.0 °C at 760 mmHg
Molecular Formula C10H19NO4 Melting Point 112-114℃
MSDS Chinese USA Flash Point 160.5±23.2 °C

 Use of N-Boc-L-valine


2-((tert-Butoxycarbonyl)amino)-3-methylbutanoic acid is a valine derivative[1].

 Names

Name 3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
Synonym More Synonyms

 N-Boc-L-valine Biological Activity

Description 2-((tert-Butoxycarbonyl)amino)-3-methylbutanoic acid is a valine 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 341.8±25.0 °C at 760 mmHg
Melting Point 112-114℃
Molecular Formula C10H19NO4
Molecular Weight 217.262
Flash Point 160.5±23.2 °C
Exact Mass 217.131409
PSA 79.12000
LogP 1.98
Appearance of Characters Solid
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.461
Storage condition Store at RT.

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 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%

 Synonyms

Boc-DL-valine
(2S)-2-[(tert-butoxy)carbonylamino]-3-methylbutanoic acid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-valine
(S)-2-(Boc-amino)-3-methylbutyric acid
BOC-DL-VAL-OH
N-tert-Butoxycarbonylvaline
N-t-Butoxycarbonyl-L-valine
BOC-L-Valine
Boc-Val-OH
Valine, N-[(1,1-dimethylethoxy)carbonyl]-
N-α-(t-Butoxycarbonyl)-DL-valine
L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
tert-Butoxycarbonylvaline
N-(tert-Butoxycarbonyl)-L-valin
Boc-L-Val-OH
tert-Butoxycarbonyl-L-valine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}valine
Boc-L-Valine-OH
N-tert-Butoxycarbonyl-L-valine
N-Boc-DL-valine
(2S)-3-Methyl-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid
N-Boc-valine
N-tert-Butyloxycarbonyl-L-valine
N-(tert-Butoxycarbonyl)-L-valine
N-(tert-butoxycarbonyl)valine
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