Weight | 194.23 g/mol |
---|---|
Formula | C11H14O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
tert-Butyl peroxybenzoate (614-45-9)
peroxybenzoic acid t-butyl ester
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- tert-Butyl peroxybenzoate (TBPB)-mediated 2-isocyanobiaryl insertion with 1,4-dioxane: efficient synthesis of 6-alkyl phenanthridines via C(sp3)-H/C(sp2)-H bond functionalization. (Chemical Communications, 2014)
- Reaction of nucleophiles with electron acceptors by SN2 or electron transfer (ET) mechanisms: tert-butyl peroxybenzoate/dimethyl sulfide and benzoyl peroxide/N,N-dimethylaniline systems (Journal of the American Chemical Society, 1983)
- Modeling liquid thermal explosion reactor containing tert-butyl peroxybenzoate (Journal of Thermal Analysis and Calorimetry, 2010)
- tert-Butyl peroxybenzoate-promoted -methylation of 1,3-dicarbonyl compounds. (Journal of Organic Chemistry, 2014)
- Runaway reaction on tert -butyl peroxybenzoate by DSC tests (Journal of Thermal Analysis and Calorimetry, 2008)
- Green thermal analysis for predicting thermal hazard of storage and transportation safety for tert-butyl peroxybenzoate (Journal of Loss Prevention in The Process Industries, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H227: Combustible liquid
Warning Flammable liquids - Category 4 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - peroxybenzoic acid t-butyl ester
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SMILESCC(C)(C)OOC(=O)C1=CC=CC=C1
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InChIKeyGJBRNHKUVLOCEB-UHFFFAOYSA-N
- Pubchem - tert-Butyl peroxybenzoate
- Wikipedia - tert-butyl peroxybenzoate
tert-Butyl peroxybenzoate (TBPB) a chemical compound from the group of peresters (compounds containing the general structure R1-C(O)OO-R2) which contains a phenyl group as R1 and a tert-butyl group as R2. It is often used as a radical initiator in polymerization reactions, such as the production of LDPE from ethylene, and for crosslinking, such as for unsaturated polyester resins.
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