Bis(2-methacryloyl)oxyethyl disulfide

ALDRICH/735094 - contains ≤6000 ppm hydroquinone as stabilizer

Synonym: DSDMA; Disulfide-based dimethacrylate

CAS Number: 36837-97-5
Empirical Formula (Hill Notation): C₁₂H₁₈O₄S₂
Molecular Weight: 290.40
MDL Number: MFCD18785736
Linear Formula: C₁₂H₁₈O₄S₂
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-735094-5G	5 g	$369.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

contains	≤6000 ppm hydroquinone as stabilizer
density	1.141 g/mL at 25 °C
form	liquid
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
InChI key	CGDNFXSLPGLMHK-UHFFFAOYSA-N
Quality Level	100
refractive index	n20/D 1.517
SMILES string	CC(=C)C(=O)OCCSSCCOC(=O)C(C)=C
storage temp.	2-8°C

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.
General description:	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.
Packaging:	5 g in glass bottle

Hazard statements	H412
Precautionary statements	P273 - P501
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Density	1.141 g/mL at 25 °C
Refractive Index	n20/D 1.517
Storage Temp.	2-8°C
UNSPSC	12162002

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