868-63-3

Basic information

• Product Name: N,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE
• Synonyms: DHEBA, N,Nμ-Bisacryloyl-1,2-dihydroxy-1,2-ethylenediamine;Dheba(N,NDihydroxyethylene-Bis-Acrylamide);N,N'-(1,2-Dihydroxy-1,2-ethanediyl)bis(2-propenamide);N,N'-(1,2-Dihydroxyethylene)bispropenamide;N,N'-Dihydroxyethylene-bis-acrylamide,for biochemistry,electrophoresis grade;N,N′-(1,2-Dihydroxyethylene)bis-acrylamide,DHEBA, N,N′-Bisacryloyl-1,2-dihydroxy-1,2-ethylenediamine;N,N′-(1,2-Dihydroxyethylene)bisacrylamide,N,N′-Bisacryloyl-1,2-dihydroxy-1,2-ethylenediamine, DHEBA;1,2-Bisacrylamido-1,2-ethanediol N,N'-Diacryloyl-1,2-dihydroxyethylenediamine
• CAS NO: 868-63-3
• Molecular Formula: C₈H₁₂N₂O₄
• Molecular Weight: 200.19
• EINECS: 212-780-1
• Product Categories: Acrylic Monomers;Biomaterials;Crosslinking Agents;Materials Science;Monomers;Polyfunctional Acrylics;Polymer Science
• Mol File: 868-63-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 156 °C (dec.)(lit.)
• Boiling Point: 156 °C
• Flash Point: 326.4 °C
• Appearance: White/Powder
• Density: 1.263 g/cm³
• Storage Temp.: 2-8°C
• Solubility: DMSO (Slightly), Methanol (Slightly), Water (Slightly)
• PKA: 11.76±0.20(Predicted)
• Water Solubility: Soluble in water and sodium hydroxide.
• BRN: 1941875
• CAS DataBase Reference: N,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE(868-63-3)
• EPA Substance Registry System: N,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE(868-63-3)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 868-63-3(Hazardous Substances Data)

Usage

Chemical Properties

white powder

Relevant articles and documents

One step process for preparing cross-linked poly-β-alanine microspheres from acrylamide and a copolymerisable polyfunctional compound

A one-step process for preparing cross-linked poly-β-alanine as microspheres having narrow size distribution comprises polymerizing acrylamide with a polyfunctional compound copolymerizable with acrylamide (with the polyfunctional compound also acting as the cross-linking agent) in an organic solvent or a mixtured such solvents in the presence of an ionic polymerization initiator and a suspension agent. The resulting microspheres may be impregnated with a pharmaceutically or cosmetically active substance.