| Bioactivity | Methacrylic anhydride is a typical polymerizable 1,6-diolefin. Methacrylic anhydride can form a soluble csyclopolymer by free-radical initiation. Methacrylic anhydride can spontaneously polymerize through the vinyl group and justifies the use of 2-6-di-tert-butyl4-methylphenol as an inhibitor[1][2]. | ||||||||||||
| Name | Methacrylic anhydride | ||||||||||||
| CAS | 760-93-0 | ||||||||||||
| Formula | C8H10O3 | ||||||||||||
| Molar Mass | 154.17 | ||||||||||||
| Appearance | Liquid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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| Reference | [1]. Jesse C. H. Hwa, et al. Copolymerization of methacrylic anhydride with vinyl monomers. Journal of Polymer Science. November 1961, 55(161):197-213. [2]. F. Becquart, et al. Functionalization of a poly(vinyl alcohol) in the solid state with a swelling agent by methacrylic anhydride. Polymer Chemistry. 1 April 2004, 42(7):1618-1629. |
Methacrylic anhydride
CAS: 760-93-0 F: C8H10O3 W: 154.17
Methacrylic anhydride is a typical polymerizable 1,6-diolefin. Methacrylic anhydride can form a soluble csyclopolymer by
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