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698717
Polyoxyethanyl-α-tocopheryl sebacate
15 wt. % in H2O
Sinonimo/i:
PTS
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About This Item
Prodotti consigliati
Stato
liquid
Livello qualitativo
PM
~1,200
Impiego in reazioni chimiche
reaction type: C-C Bond Formation
Caratteristiche più verdi
Waste Prevention
Designing Safer Chemicals
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
Concentrazione
15 wt. % in H2O
Categoria alternativa più verde
Descrizione generale
Applicazioni
Uses:
- Provides an aqueous micellar environment for transition metal-catalyzed Heck coupling, cross metathesis and ring closing metathesis reactions
- Surfactant for catalytic asymmetric Baeyer-Villiger oxidation in water using PtII catalysts and hydrogen peroxide
- Orally active CoQ10 carrier for neuroprotection after stroke or cardiac arrest
Note legali
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Articoli
Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.
Surfactants for efficient reactions in water as a green chemistry alternative.
The Baeyer-Villiger oxidation is the oxidative cleavage of a carbon-carbon bond adjacent to a carbonyl, which converts the ketones to esters and the cyclic ketones to lactones.
Contenuto correlato
Designer surfactants enable diverse transformations like Suzuki-Miyaura, Olefin Metathesis, and 1,4-Addition to Enones in water by Prof. Bruce Lipshutz.
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What can Product 698717, Polyoxyethanyl-α-tocopheryl sebacate, be used for?
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PTS is a non-ionic amphiphile that can be used to "solubilize" organic molecules in aqueous media. The PTS molecule forms micelles around the lipophilic compounds, allowing them to move into the aqueous phase for effective cross-coupling and metathesis reactions without the need of a co-solvent.
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