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Merck

116122

Sigma-Aldrich

D-2-Aminobutyric acid

98%

Sinónimos:

(R)-(−)-2-Aminobutyric acid

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About This Item

Fórmula lineal:
C2H5CH(NH2)CO2H
Número de CAS:
Peso molecular:
103.12
Beilstein/REAXYS Number:
1720934
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

optical activity

[α]20/D −21 to −19°, c = 4 in H2O

optical purity

ee: 98% (GLC)

reaction suitability

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC[C@@H](N)C(O)=O

InChI

1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m1/s1

InChI key

QWCKQJZIFLGMSD-GSVOUGTGSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Chen Qi et al.
Polymers, 12(9) (2020-09-13)
Eight kinds of chiral diacid monomers were prepared with amino acids with different side groups or configurations. Polyester-imides (PEIs) were synthesized from these diacid monomers and diphenol monomers through polycondensation reaction, and the performances and properties were compared with the
Zhiying Wang et al.
Communications biology, 3(1), 39-39 (2020-01-24)
Osteoporosis is a highly prevalent chronic aging-related disease that frequently is only detected after fracture. We hypothesized that aminobutyric acids could serve as biomarkers for osteoporosis. We developed a quick, accurate, and sensitive screening method for aminobutyric acid isomers and
Babu Joseph et al.
The Journal of general and applied microbiology, 52(6), 315-320 (2007-02-28)
Staphylococcus epidermidis isolated from spoiled frozen marine fish samples exhibited optimum lipase activity of 8.1 U within 72 h in batch fermentation. Inducible effect of different sugars, nitrogen sources, salts and metal ions were studied on enzyme production. Trybutyrin induced
Gang Wei et al.
The Journal of biological chemistry, 284(42), 29180-29192 (2009-07-31)
Despite the small size and conserved tertiary structure of defensins, little is known at a molecular level about the basis of their functional versatility. For insight into the mechanism(s) of defensin function, we prepared enantiomeric pairs of four human defensins
Li Zhu et al.
Applied microbiology and biotechnology, 90(3), 903-910 (2011-02-10)
L-2-Aminobutyric acid can be synthesized in a transamination reaction from L-threonine and L-aspartic acid as substrates by the action of threonine deaminase and aromatic aminotransferase, but the by-product L-alanine was produced simultaneously. A small amount of L-alanine increased the complexity

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