L-2,4-Diaminobutyric Acid, Dihydrochloride

CAS: 1883-09-6

Ref. TR-D416250

Product Information

• Name: L-2,4-Diaminobutyric Acid, Dihydrochloride
• Synonyms: (2S)-2,4-diaminobutanoic acid;dihydrochloride, (2S)-2,4-diaminobutanoic acid dihydrochloride, (2S)-2,4-diammoniobutanoate, (S)-(+)-2,4-Diamino-N-Butyric Acid Dihydrochloride, (S)-(+)-2,4-Diaminobutyric Acid Dihydrochloride, (S)-(+)-2,4-Diaminobutyric Acid Hydrochloride, <span class="text-smallcaps">L</span>-2,4-Diaminobutanoic acid dihydrochloride, <span class="text-smallcaps">L</span>-2,4-Diaminobutyric acid dihydrochloride, Alpha,Gamma-Diaminobutyric Acid Hydrochloride Salt, Butanoic acid, 2,4-diamino-, dihydrochloride, (2S)-, Butanoic acid, 2,4-diamino-, dihydrochloride, (S)-, Butanoic acid, 2,4-diamino-, hydrochloride (1:2), (2S)-, Butyric acid, 2,4-diamino-, dihydrochloride, <span class="text-smallcaps">L</span>-, H-Dab-OH 2HCL, H-Daba-OH.2HCl, L-2,4-Diaminobutyric Acid Hydrochloride, L-2,4-Diaminobutyric Acid Monohydrochloride, L-Alpha, Gamma-Diaminobutyric Acid Dihydrochloride

Description

Applications 2,4-Diaminobutyric Acid is a pharmacological tool and potential chiral building block. 2,4-Diaminobutyric Acid is also used as an internal standard for amino acid analysis. 2,4-Diaminobutyric Acid is also found to inhibit GABA transaminase, thus producing an elevation of GABA level, and to have an antitumor activity in vitro and in vivo against mouse fibrosarcoma cells.
References Riordan, J.F., et al.: Methods Enzymol., 47, 31 (1977), Beart, P.M., et al.: Neurscience Lett., 5, 193 (1977), Ronquist, G., et al.: J. Cancer Res. Clin. Oncol., 96, 259 (1980), Solladie-Cavallo, A., et al.: Tetrahedron Lett., 30, 6011 (1989)

• Brand: TRC

Chemical properties

• Molecular weight: 191.06
• Formula: C₄H₁₀N₂O₂ClH
• Color/Form: Neat
• InChI: InChI=1S/C4H10N2O2.2ClH/c5-2-1-3(6)4(7)8;;/h3H,1-2,5-6H2,(H,7,8);2*1H/t3-;;/m0../s1
• InChI key: InChIKey=OGNSCSPNOLGXSM-VKHMYHEASA-N
• SMILES: NCC[C@H](N)C(=O)O