A2536

L-2-Aminobutyric acid

BioReagent, suitable for cell culture

• Synonyme(s) : L-α-Aminobutyric acid
• Formule empirique (notation de Hill) : C₄H₉NO₂
• CAS Number: 1492-24-6
• Poids moléculaire : 103.12
• Beilstein: 1720935
• Numéro CE : 216-083-3
• Numéro MDL: MFCD00064415
• Code UNSPSC : 12352205
• ID de substance PubChem : 24890666
• Nomenclature NACRES : NA.75

Propriétés

• Source biologique: Porcine kidney; microbial; plant
• Gamme de produits: BioReagent
• Forme: powder
• Technique(s): cell culture | mammalian: suitable
• Solubilité: water: 50 mg/mL, clear, colorless
• Conditions d'expédition: ambient
• Température de stockage: room temp
• Chaîne SMILES: 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-/m0/s1
• Clé InChI: QWCKQJZIFLGMSD-VKHMYHEASA-N

Description

Description générale

L-2-Aminobutyric acid is synthesized from L-threonine and L-aspartic acid through a ⍺-transamination reaction. It is an L-alanine analogue with an ethyl side chain.

Actions biochimiques/physiologiques

L-α-Aminobutyric acid (AABA) is an isomer of the non-natural amino acid aminobutyric acid with activity in the γ-glutamyl cycle that regulates glutathione biosynthesis. Recently AABA has been studied as a supplement to in vitro maturation medium (NCSU 23 medium) for culture of oozytes and embryos. This product has been qualified for use in cell culture. AABA is also used as a substitute amino acid for alanine in studies on peptide function.

Informations sur la sécurité

• Pictogrammes: GHS07
• Mention d'avertissement: Warning
• Mentions de danger: H317
• Conseils de prudence: P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364
• Classification des risques: Skin Sens. 1
• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Faceshields, Gloves