162663
DL-2-Aminobutyric acid
99%, for peptide synthesis, ReagentPlus®
Synonym(s):
AABA, Homoalanine, alpha-amino-n-butyric acid
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About This Item
Linear Formula:
C2H5CH(NH2)CO2H
CAS Number:
Molecular Weight:
103.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
220-616-5
MDL number:
Beilstein/REAXYS Number:
635889
Product Name
DL-2-Aminobutyric acid, ReagentPlus®, 99%
InChI key
QWCKQJZIFLGMSD-UHFFFAOYSA-N
InChI
1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
SMILES string
CCC(N)C(O)=O
product line
ReagentPlus®
assay
99%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
291 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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General description
DL-2-Aminobutyric acid also known as α-aminobutyric acid, is commonly used in solution-phase peptide synthesis.
Application
DL-2-Aminobutyric acid can be used to synthesize 2-(2,5-dioxopyrrolidin-1-yl) butanoic acid.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Design, synthesis, and anticonvulsant activity of new hybrid compounds derived from 2-(2, 5-dioxopyrrolidin-1-yl) propanamides and 2-(2, 5-dioxopyrrolidin-1-yl) butanamides
Journal of Medicinal Chemistry, 58, 5274-5286 (2015)
Ryan J Martinie et al.
Journal of the American Chemical Society, 137(21), 6912-6919 (2015-05-13)
The iron(II)- and 2-(oxo)glutarate-dependent (Fe/2OG) oxygenases catalyze an array of challenging transformations, but how individual members of the enzyme family direct different outcomes is poorly understood. The Fe/2OG halogenase, SyrB2, chlorinates C4 of its native substrate, l-threonine appended to the
Christian Rausch et al.
Proteins, 81(5), 774-787 (2012-12-15)
Apart from their crucial role in metabolism, pyridoxal 5'-phosphate (PLP)-dependent aminotransferases (ATs) constitute a class of enzymes with increasing application in industrial biotechnology. To provide better insight into the structure-function relationships of ATs with biotechnological potential we performed a fundamental
Izumi Kawabata et al.
Nature communications, 3, 722-722 (2012-03-08)
Synaptic remodelling coordinated with dendritic growth is essential for proper development of neural connections. After establishment of synaptic contacts, synaptic junctions are thought to become stationary and provide fixed anchoring points for further dendritic growth. However, the possibility of active
Young-Man Seo et al.
Organic & biomolecular chemistry, 10(12), 2482-2485 (2012-02-22)
A deracemization method was developed to generate optically pure L-homoalanine from racemic homoalanine using D-amino acid oxidase and ω-transaminase. A whole cell reaction using a biphasic system converted 500 mM racemic homoalanine to 485 mM L-homoalanine (>99% ee).
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