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일반 설명
Triisopropyl phosphate, an ester of secondary alcohol, is a non-phosphorylating organophosphorus compound. It is formed as a by-product during the synthesis of haloalkylphosphonates. Triisopropyl phosphate can be prepared from isopropyl alcohol by reacting with phosphorus oxychloride. It can also be obtained from triisopropyl phosphite.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
141.8 °F - closed cup - (own results)
Flash Point (°C)
61 °C - closed cup - (own results)
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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이미 열람한 고객
Physicochemical characteristics and sorption capacities of heavy metal ions of activated carbons derived by activation with different alkyl phosphate triesters
Applied Surface Science, 316, 443-450 (2014)
Efficient and `green?microwave-assisted synthesis of haloalkylphosphonates via the Michaelis?Arbuzov reaction.
Green Chemistry, 13(4), 882-888 (2011)
Reactions of Trialkyl Phosphates, Alkyl Acetates, and Tertiary Butyl Hypochlorite in the Friedel-Crafts Syntheses1.
Journal of the American Chemical Society, 60(11), 2596-2597 (1938)
Dealkylation and debenzylation of triesters of phosphoric acid. Phosphorylation of hydroxy and amino compounds.
Journal of the American Chemical Society, 77(20), 5354-5357 (1955)
Carbonium ion formation in solvolysis of phosphate triesters.
The Journal of Organic Chemistry, 34(9), 2600-2605 (1969)
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