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Sigma-Aldrich

Luperox® DI, tert-Butyl peroxide

98%

Sinônimo(s):

tert-Butyl peroxide, Di-tert-butyl peroxide

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About This Item

Fórmula linear:
(CH3)3COOC(CH3)3
Número CAS:
110-05-4
Peso molecular:
146.23
Beilstein:
1735581
Número CE:
203-733-6
Número MDL:
MFCD00008803
Código UNSPSC:
12352120
ID de substância PubChem:
24850244
NACRES:
NA.22

pressão de vapor

40 mmHg ( 20 °C)

Ensaio

98%

forma

liquid

adequação da reação

reagent type: oxidant

índice de refração

n20/D 1.3891 (lit.)

pb

109-110 °C (lit.)

densidade

0.796 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CC(C)(C)OOC(C)(C)C

InChI

1S/C8H18O2/c1-7(2,3)9-10-8(4,5)6/h1-6H3

chave InChI

LSXWFXONGKSEMY-UHFFFAOYSA-N

Aplicação

Luperox®DI, tert-Butyl peroxide has been used as a radical initiator to induce free radical polymerization. It has also been used as a cetane enhancer in a study to determine the phase behavior of carboxylate-based extended surfactant reverse micellar microemulsions with ethanol and vegetable oil/diesel blends.

Informações legais

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Pictogramas

FlameHealth hazard
GHS02,GHS08

Palavra indicadora

Danger

Frases de perigo

H225,H242,H341,H412

Classificações de perigo

Aquatic Chronic 3 - Flam. Liq. 2 - Muta. 2 - Org. Perox. E

Código de classe de armazenamento

5.2 - Organic peroxides and self-reacting hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

42.8 °F - closed cup

Ponto de fulgor (°C)

6 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Vegetable oil-based microemulsions using carboxylate-based extended surfactants and their potential as an alternative renewable biofuel.
Attaphong C
Fuel: The Science and Technology of Fuel and Energy, 94, 606-613 (2012)
Geun-Tae Yun et al.
Science advances, 4(8), eaat4978-eaat4978 (2018-08-29)
Both high static repellency and pressure resistance are critical to achieving a high-performance omniphobic surface. The cuticles of springtails have both of these features, which result from their hierarchical structure composed of primary doubly reentrant nanostructures on secondary microgrooves. Despite
A Mortensen et al.
FEBS letters, 426(3), 392-396 (1998-05-26)
Peroxyl radicals, as model for peroxyl radicals formed during autoxidation of lipids, have been generated in three solvent systems (cyclohexane, tetrahydrofuran and tert-butanol/water) by steady-state and laser flash photolysis, and their reaction with beta-carotene studied. Steady-state photolysis experiments showed that
Free radical polymerization of caffeine?containing methacrylate monomers.
Nelson AM
Journal of Polymer Science Part A: Polymer Chemistry, 53(24), 2829-2837 (2015)
Hironori Kitaguchi et al.
Journal of the American Chemical Society, 127(18), 6605-6609 (2005-05-05)
Well-resolved ESR spectra of free pentadienyl radicals have been observed under photoirradiation of di-tert-butylperoxide (Bu(t)OOBu(t)) and polyunsaturated fatty acids in the absence of O(2), allowing us to determine the hfc values. The hfc values of linoleyl radical indicate that the
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