49510

L-Glutamic acid γ-benzyl ester

≥99.0% (T)

• Sinônimo(s): L-Glutamic acid 5-benzyl ester
• Fórmula linear: C₆H₅CH₂OCOCH₂CH₂CH(NH₂)COOH
• Número CAS: 1676-73-9
• Peso molecular: 237.25
• Beilstein: 1885646
• Número CE: 216-826-1
• Número MDL: MFCD00002633
• Código UNSPSC: 12352209
• ID de substância PubChem: 57651200
• NACRES: NA.22

Propriedades

• Ensaio: ≥99.0% (T)
• atividade óptica: [α]20/D +19±2°, c = 1% in acetic acid
• adequação da reação: reaction type: solution phase peptide synthesis
• pf: 181-182 °C (lit.)
• aplicação(ões): peptide synthesis
• temperatura de armazenamento: 2-8°C
• cadeia de caracteres SMILES: N[C@@H](CCC(=O)OCc1ccccc1)C(O)=O
• InChI: 1S/C12H15NO4/c13-10(12(15)16)6-7-11(14)17-8-9-4-2-1-3-5-9/h1-5,10H,6-8,13H2,(H,15,16)/t10-/m0/s1
• chave InChI: BGGHCRNCRWQABU-JTQLQIEISA-N

Descrição

Aplicação

L-Glutamic acid γ-benzyl ester is commonly used in the synthesis of polymers for biological applications.[1][2] Some of the examples are:

• Synthesis of bioreducible block copolymers based on poly(ethylene glycol) and poly(γ-benzyl L-glutamate) for Intracellular drug delivery.[3]
• Synthesis of biodegradable poly(L-glutamic acid)-b-polylactide for magnetic resonance imaging (MRI)-visible drug delivery system.[4]
• Synthesis of pH and temperature-responsive diblock copolymers based on poly(L-glutamic acid).[5]

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Gloves, type N95 (US)