735094

Bis(2-methacryloyl)oxyethyl disulfide

contains ≤6000 ppm hydroquinone as stabilizer

• Synonyme(s) : DSDMA, Disulfide-based dimethacrylate
• Formule empirique (notation de Hill): C₁₂H₁₈O₄S₂
• Numéro CAS: 36837-97-5
• Poids moléculaire : 290.40
• Numéro MDL: MFCD18785736
• Code UNSPSC : 12162002
• ID de substance PubChem : 329763793
• Nomenclature NACRES : NA.23

Propriétés

• Forme: liquid
• Niveau de qualité: 100
• Contient: ≤6000 ppm hydroquinone as stabilizer
• Indice de réfraction: n20/D 1.517
• Densité: 1.141 g/mL at 25 °C
• Température de stockage: 2-8°C
• Chaîne SMILES: CC(=C)C(=O)OCCSSCCOC(=O)C(C)=C
• InChI: 1S/C12H18O4S2/c1-9(2)11(13)15-5-7-17-18-8-6-16-12(14)10(3)4/h1,3,5-8H2,2,4H3
• Clé InChI: CGDNFXSLPGLMHK-UHFFFAOYSA-N

Description

Description générale

Bis(2-methacryloyl)oxyethyl disulfide (DSDMA) belongs to the class of monomers known as disulfide-based dimethacrylates. It is widely employed as a crosslinker in the synthesis of various polymers with specific properties such as redox sensitivity and self-healing properties. DSDMA contains a disulfide bond, which can be cleaved under specific conditions, making it useful for drug delivery systems. It also undergoes thiol-disulfide exchange reactions, allowing it to react with thiols in polymers and form covalent crosslinks. This property enables the formation of networks and gels in polymer systems. Additionally, DSDMA is employed in the development of biomedical materials, such as tissue engineering scaffolds. Its ability to form stable crosslinks in biological environments makes it suitable for these applications.

Application

Bis(2-methacryloyl)oxyethyl disulfide (DSDMA) can be used in the following applications:

• Used as a crosslinker in the synthesis of reduction-responsive molecularly imprinted polymer (MIPs) nanogels for drug delivery applications. This reduction-responsive property allows for control over drug delivery and modulation of the release properties of the MIPs.
• Used as a crosslinker in the synthesis of self-healing polymer nanocomposites via dynamic disulfide exchange reaction and crosslinking properties. These self-healing polymer nanocomposites can be used in coatings, electronics, and packaging applications.
• Used as a redox-responsive cross-linker in the synthesis of zwitterionic hydrogels for effective drug delivery. DSDMA provides structural stability, redox-responsiveness, and self-healing properties, which are essential for effective drug delivery.

Informations sur la sécurité

• Pictogrammes: GHS09
• Mentions de danger: H411
• Conseils de prudence: P273 - P391 - P501
• Classification des risques: Aquatic Chronic 2
• Code de la classe de stockage: 10 - Combustible liquids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable