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Merck

217794

Sigma-Aldrich

DL-3-Aminoisobuttersäure

98%

Synonym(e):

α-Methyl-β-alanin

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About This Item

Lineare Formel:
NH2CH2CH(CH3)COOH
CAS-Nummer:
Molekulargewicht:
103.12
Beilstein:
1720958
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352106
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

98%

Form

powder

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

179-182 °C (lit.)

Anwendung(en)

peptide synthesis

SMILES String

CC(CN)C(O)=O

InChI

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

InChIKey

QCHPKSFMDHPSNR-UHFFFAOYSA-N

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Y Kurozumi et al.
Acta medica Okayama, 53(1), 13-18 (1999-03-30)
Experimental beta-alaninuria was induced in rats by injection of (aminooxy)acetate (AOA), a potent inhibitor of aminotransferases, in order to elucidate the pathogenesis of hyper-beta-alaninemia. A 27-fold increase of beta-alanine (BALA) excretion was induced by subcutaneous injection of 1 5 mg
T Abe et al.
Journal of chromatography. B, Biomedical sciences and applications, 712(1-2), 43-49 (1998-08-11)
A method is described for the simultaneous determination of beta-alanine, beta-aminoisobutyric acid and gamma-aminobutyric acid in biological materials. Amino acids including these beta- and gamma-amino acids were derivatized with 4-dimethylaminoazobenzene-4'-sulfonyl (dabsyl) chloride and dabsyl amino acids formed were separated by
A J Dobson et al.
Acta crystallographica. Section C, Crystal structure communications, 54 ( Pt 7), 972-974 (1998-09-18)
The title acid, 3-amino-2-methylpropanoic acid monohydrate, C4H9NO2.H2O, crystallized in the centrosymmetric space group Pbca in the zwitterionic form. The three H atoms on N, which are involved in hydrogen bonding, are ordered. The three intermolecular N-H...O hydrogen bonds have N...O
P M Zeis et al.
Cytobios, 102(400), 107-113 (2000-07-08)
Previous investigators agree on the increased DNA synthesis and destruction of tissues caused by folic acid (FA) administered parenterally. This study aims to clarify whether DNA degradation due to the destruction of cells and nuclei precedes DNA synthesis following FA
E Lahat et al.
Pediatric neurology, 21(1), 460-463 (1999-07-31)
Vigabatrin (gamma-vinyl gamma aminobutyric acid), a recently developed antiepileptic drug, has been extensively evaluated in the treatment of drug-resistant epilepsy. Several case reports demonstrated that vigabatrin affects urinary excretion of several amino and organic acids. Fourteen children were investigated for

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