Boc-D-Valine

Modify Date: 2024-01-02 21:09:17

Boc-D-Valine Structure
Boc-D-Valine structure
Common Name Boc-D-Valine
CAS Number 22838-58-0 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 164-165ºC
MSDS Chinese USA Flash Point 160.5±23.2 °C

 Use of Boc-D-Valine


tert-Butoxycarbonyl-D-valine is a valine derivative[1].

 Names

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

 Boc-D-Valine Biological Activity

Description tert-Butoxycarbonyl-D-valine 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 164-165ºC
Molecular Formula C10H19NO4
Molecular Weight 217.262
Flash Point 160.5±23.2 °C
Exact Mass 217.131409
PSA 75.63000
LogP 1.98
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.461
Storage condition 2~8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Preparation


 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%

 Articles1

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...

 Synonyms

(2S)-2-[(tert-butoxy)carbonylamino]-3-methylbutanoic acid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-valine
(R)-2-((tert-Butoxycarbonyl)amino)-3-methylbutanoic acid
(S)-2-(Boc-amino)-3-methylbutyric acid
(2R)-2-[(TERT-BUTOXYCARBONYL)AMINO]-3-METHYLBUTANOIC ACID
Boc-D-Valine
N-t-Butoxycarbonyl-L-valine
BOC-L-Valine
tert-butyloxycarbonyl-D-valine
Boc-D-Val-OH
N-Boc-D-valine
L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
N-(tert-Butoxycarbonyl)-L-valin
Boc-L-Val-OH
MFCD00038282
Boc-L-Valine-OH
N-tert-Butoxycarbonyl-L-valine
N-t-butyloxycarbonyl-D-valine
N-α-(t-Butoxycarbonyl)-D-valine
(R)-Boc-Val-OH
(2S)-3-Methyl-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid
N-Boc-valine
tBoc-DVal-OH
D-Valine, N-BOC protected
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-valine
N-(tert-Butoxycarbonyl)-D-valine
N-tert-Butyloxycarbonyl-L-valine
N-(tert-Butoxycarbonyl)-L-valine
D-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
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