2-amino-2-methylpropionic acid
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| General | ||||||||||||||||||||||
| Surname | 2-amino-2-methylpropionic acid | |||||||||||||||||||||
| other names |
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| Molecular formula | C 4 H 9 NO 2 | |||||||||||||||||||||
| Brief description |
White dust |
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| properties | ||||||||||||||||||||||
| Molar mass | 103.2 g mol −1 | |||||||||||||||||||||
| Physical state |
firmly |
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| density |
1.109 g cm −3 |
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| Melting point |
> 300 ° C |
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| solubility |
soluble in water |
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||||||||||||||
2-Amino-2-methylpropionic acid is a chemical compound . It belongs to the non-proteinogenic amino acids . The α-carbon atom is also not a stereocenter; so it is not chiral.
Extraction
On a laboratory scale, 2-amino-2-methylpropionic acid can be obtained from acetone cyanohydrin and ammonium with subsequent hydrolysis.
Individual evidence
- ↑ a b c data sheet α-aminoisobutyric acid from Sigma-Aldrich , accessed on April 23, 2013 ( PDF ).
- ↑ Entry 2-amino isobutyric acid at Pharmasi Chemicals Co., accessed May 8, 2013.
- ↑ a b Entry on 2-Amino-2-methylpropionic acid at ChemicalBook , accessed April 23, 2013.
- ↑ Clarke, HT; Bean, H. J: α-Aminoisobutyric Acid In: Organic Syntheses . 11, 1931, p. 4, doi : 10.15227 / orgsyn.011.0004 ; Coll. Vol. 2, 1943, p. 29 ( PDF ).