4,4'-Diaminodiphenyl Sulfone(DDS) - Moligand™, ≥99.5%, used for Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O
4,4'-Diaminodiphenyl Sulfone(DDS) - Moligand™, ≥99.5%, used for Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O
QUALITÄT & REINHEITMoligand™?Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.≥99.5%
4-Aminobenzenesulfone (DDS) is a diamine curing agent used for curing epoxy resins.
Product application:
Product application: Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O3), forming flame-retardant epoxy resin nanocomposites. It can also be used as a curing agent to cure bisphenol A (DGEBA) used in the manufacture of flame-retardant epoxy resin/clay nanocomposites.
Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O3), forming flame-retardant epoxy resin nanocomposites. It can a
Storage
Store at 2-8°C,Protected from light
Verschickt in
Wet ice
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This compound belongs to the class of organic compounds known as benzenesulfonyl compounds. These are aromatic compounds containing a benzenesulfonyl group, which consists of a monocyclic benzene moiety that carries a sulfonyl group.
External Descriptors
sulfone - substituted aniline
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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