Boc-Aib-OH

Modify Date: 2024-01-06 18:31:19

Boc-Aib-OH Structure
Boc-Aib-OH structure
 Common Name Boc-Aib-OH
CAS Number 30992-29-1 Molecular Weight 203.236
Density 1.1±0.1 g/cm3 Boiling Point 325.6±37.0 °C at 760 mmHg
Molecular Formula C9H17NO4 Melting Point 118-122 °C
MSDS Chinese USA Flash Point 150.7±26.5 °C

 Use of Boc-Aib-OH


2-((tert-Butoxycarbonyl)amino)-2-methylpropanoic acid is an alanine derivative[1].

 Names

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

 Boc-Aib-OH Biological Activity

Description 2-((tert-Butoxycarbonyl)amino)-2-methylpropanoic acid is an alanine 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):1793-1105.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 325.6±37.0 °C at 760 mmHg
Melting Point 118-122 °C
Molecular Formula C9H17NO4
Molecular Weight 203.236
Flash Point 150.7±26.5 °C
Exact Mass 203.115753
PSA 75.63000
LogP 1.29
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.477
Storage condition 0-6°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

 Synthetic Route

 Articles2

More Articles
Unraveling the interplay of backbone rigidity and electron rich side-chains on electron transfer in peptides: the realization of tunable molecular wires.

J. Am. Chem. Soc. 136(35) , 12479-88, (2014)

Electrochemical studies are reported on a series of peptides constrained into either a 310-helix (1-6) or β-strand (7-9) conformation, with variable numbers of electron rich alkene containing side cha...

W. Mayr, G. Jung

Liebigs Ann. Chem. (and reference cited therein) , 715, (1980)

 Synonyms

N-Boc-2-Aminoisobutanoic acid
Boc-Aib-OH
2-(1,1-dimethylethoxycarbonyl)amino-2-methyl-propionic acid
BOC-α-Methylalanine
N-((1,1-Dimethylethoxy)carbonyl)-2-methyl-alanine
Aspartic acid, 2-methyl-, 4-(1,1-dimethylethyl) ester
N-Boc-2-methylalanine
2-Amino-2-methyl-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid
2-(tert-butoxycarbonyl)amino-2-methylpropanoic acid
α-(Boc-amino)isobutyric acid
2-(tert-Butoxycarbonylamino)isobutyric Acid
N-(tert-butoxycarbonyl)-2-aminoisobutyric acid
2-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}alanine
Boc-Alpha-Methylalanine
Alanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-
2-tert-butoxycarbonylamino-2-methyl-propionic acid
Boc-2-aminoisobutyric acid
N-Boc-2-amino-2-methylpropanoic acid
2-((tert-Butoxycarbonyl)amino)-2-methylpropanoic acid
2-[(1,1-dimethylethoxy)carbonyl]amino-2-methyl-propanoic acid
N-Boc-α-methylalanine
2-(Boc-amino)isobutyric Acid
N-Boc-2-aminoisobutyric acid
N-(tert-butoxycarbonyl)-2-methylalanine
EINECS 250-421-0
MFCD00042973
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