A0879

N-(4-Aminobenzoyl)-L-glutamic acid

≥98% (TLC)

• Synonyme(s) : N-(p-Aminobenzoyl)glutamic acid
• Formule empirique (notation de Hill) : C₁₂H₁₄N₂O₅
• Numéro CAS: 4271-30-1
• Poids moléculaire : 266.25
• NACRES: NA.26
• PubChem Substance ID: 24890463
• UNSPSC Code: 12352209
• EC Number: 224-261-7
• MDL number: MFCD00042821
• Beilstein/REAXYS Number: 2816320

Propriétés

• Nom du produit: N-(4-Aminobenzoyl)-L-glutamic acid, ≥98% (TLC)
• Quality Segment: 200
• assay: ≥98% (TLC)
• form: powder
• color: off-white to beige
• mp: 175 °C (dec.)
• application(s): detection; peptide synthesis
• storage temp.: −20°C
• SMILES string: Nc1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O
• InChI: 1S/C12H14N2O5/c13-8-3-1-7(2-4-8)11(17)14-9(12(18)19)5-6-10(15)16/h1-4,9H,5-6,13H2,(H,14,17)(H,15,16)(H,18,19)/t9-/m0/s1
• InChI key: GADGMZDHLQLZRI-VIFPVBQESA-N

Description

Application

N-(4-Aminobenzoyl)-L-glutamic acid (ABG) is used as a strong UV absorbing tag for the derivitization of oligosaccharides to enhance their detection in analytical methods such as capillary zone electrophoresis (CZE).

Biochem/physiol Actions

N-p-Aminobenzoyl)-L-glutamic acid is a folate catabolite that can be metabolized by bacterial p-aminobenzoate auxotrophs possessing the enzyme p-aminobenzoyl-glutamate hydrolase.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)