773263

N-(2-Hydroxyethyl)maleimide

97%

• Sinónimos: 1-(2-Hydroxyethyl)-pyrrole-2,5-dione, 1-(2-Hydroxyethyl)maleimide, N-(Ethanol)maleimide, HEMI
• Fórmula empírica (notación de Hill): C₆H₇NO₃
• Número de CAS: 1585-90-6
• Peso molecular: 141.12
• Número MDL: MFCD00465266
• Código UNSPSC: 12352111
• ID de la sustancia en PubChem: 329767614
• NACRES: NA.22

Propiedades

• Ensayo: 97%
• Formulario: solid
• idoneidad de la reacción: reagent type: cross-linking reagent
• mp: 66-67 °C (lit.); 67-74 °C
• grupo funcional: hydroxyl; maleimide
• temp. de almacenamiento: 2-8°C
• cadena SMILES: O=C(N1CCO)C=CC1=O
• InChI: 1S/C6H7NO3/c8-4-3-7-5(9)1-2-6(7)10/h1-2,8H,3-4H2
• Clave InChI: AXTADRUCVAUCRS-UHFFFAOYSA-N

Descripción

Aplicación

N-(2-Hydroxyethyl)maleimide can be used:

• In the synthesis of (EFA)-based multifunctional oligoester resins with maleimides as end groups by reacting with 9,10-epoxy-18-hydroxyoctadecanoic acid (EFA) and dimethyl adipate catalyzed by Candida antarctica lipase B (CalB).[1]
• As an initiator in ring-opening polymerization of δ-valerolactone catalyzed by trifluoromethanesulfonimide.[2]
• In one-pot synthesis of bio-based polyurethane-imides by reacting with castor oil, eleostearic acid diethanol amide and isophorone diisocyanate.[3]

N-(2-Hydroxyethyl)maleimide may be used to synthesize [2,2-bis(maleimidoethoxy)-
propane (BMEP)], a protein cross-linking reagent with potential application in constructing immunotoxins.[4] It may also be used in preparing thermoresponsive self-healing polyurethanes with the shape-memory property.[5]

Información de seguridad

• Pictogramas: GHS07
• Palabra de señalización: Warning
• Frases de peligro: H319
• Consejos de prudencia: P305 + P351 + P338
• Clasificaciones de peligro: Eye Irrit. 2
• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable