| Uses | Diisodecyl Phthalate is a phthalate plasticizer. Not only are pthalate plasticizers widely used in the plastics industry, but they have also been detected in soft drinks, pharmaceuticals and food products |
| Definition | ChEBI: Diisodecyl phthalate is a phthalate ester and a diester. Used as plasticizer for polyvinyl chloride in calendered film, coated fabrics, building wire jackets, wire and cable extrusion, and other applications. |
| Preparation | Diisodecyl phthalate is prepared from propylene and butenes through an oligomerisation process forming hydrocarbons with 8 to 15 carbon atoms. After distillation (in view of obtaining nonene), oxonation forms aldehydes with one more carbon atom ("isodecanal"). The latter are hydrogenated and distilled to form monohydric alcohols (mainly C10). These are reacted with phthalic anhydride (PA). The first reaction step, alcoholysis of PA to give the monoester, is rapid and goes to completion. By charging in excess alcohol and by removing the water which is formed, the equilibrium can be shifted almost completely towards the products side. |
| General Description | Diisodecyl phthalate appears as colorless liquid. May float or sink in?water. (USCG, 1999) |
| Air & Water Reactions | bis(8-methylnonyl) phthalate is insoluble in water.
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| Reactivity Profile | bis(8-methylnonyl) phthalate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Can generate electrostatic charges. [Handling Chemicals Safely 1980. p. 250].
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| Health Hazard | No symptoms reported for any rate of exposure. |
| Fire Hazard | bis(8-methylnonyl) phthalate is combustible.
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