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168521

Sigma-Aldrich

Luperox® DI, tert-Butylperoxid

98%

Synonym(e):

Di-tert.-butylperoxid, tert.-Butylperoxid

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About This Item

Lineare Formel:
(CH3)3COOC(CH3)3
CAS-Nummer:
110-05-4
Molekulargewicht:
146.23
Beilstein:
1735581
EG-Nummer:
203-733-6
MDL-Nummer:
MFCD00008803
UNSPSC-Code:
12352120
PubChem Substanz-ID:
24850244
NACRES:
NA.22

Dampfdruck

40 mmHg ( 20 °C)

Qualitätsniveau

100

Assay

98%

Form

liquid

Eignung der Reaktion

reagent type: oxidant

Brechungsindex

n20/D 1.3891 (lit.)

bp

109-110 °C (lit.)

Dichte

0.796 g/mL at 25 °C (lit.)

Lagertemp.

2-8°C

SMILES String

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

InChI

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

InChIKey

LSXWFXONGKSEMY-UHFFFAOYSA-N

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

FlameHealth hazard
GHS02,GHS08

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

5.2 - Organic peroxides and self-reacting hazardous materials

WGK

WGK 1

Flammpunkt (°F)

42.8 °F - closed cup

Flammpunkt (°C)

6 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCQ3278
MKCQ3279
MKCQ3277
MKCN1097
MKCN1098

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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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