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Sigma-Aldrich

tert-Butylhydroperoxid -Lösung

~80% in di-tert-butyl peroxide/water 3:2

Synonym(e):

1,1-Dimethylethyl-hydroperoxid, 2-Hydroperoxy-2-methylpropan, TBHP

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About This Item

Lineare Formel:
(CH3)3COOH
CAS-Nummer:
75-91-2
Molekulargewicht:
90.12
Beilstein:
1098280
MDL-Nummer:
MFCD00002130
UNSPSC-Code:
12162002
PubChem Substanz-ID:
57647814

Eignung der Reaktion

reagent type: oxidant

Konzentration

~80% in di-tert-butyl peroxide/water 3:2

Brechungsindex

n20/D 1.397

Dichte

0.90 g/mL at 20 °C

Lagertemp.

2-8°C

SMILES String

CC(C)(C)OO

InChI

1S/C4H10O2/c1-4(2,3)6-5/h5H,1-3H3

InChIKey

CIHOLLKRGTVIJN-UHFFFAOYSA-N

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Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Muta. 2 - Org. Perox. C - Skin Corr. 1C - Skin Sens. 1 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

4.1A - Other explosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

109.4 °F

Flammpunkt (°C)

43 °C

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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Qiong Tang et al.
Ultrasonics sonochemistry, 20(5), 1168-1175 (2013-03-30)
This work investigated the ultrasonic assisted oxidative desulfurization of bunker-C oil with TBHP/MoO3 system. The operational parameters for the desulfurization procedure such as ultrasonic irradiation time, ultrasonic wave amplitude, catalyst initial concentration and oxidation agent initial concentration were studied. The
Younghwa Kim et al.
Food chemistry, 137(1-4), 136-141 (2012-12-04)
Oligomeric and polymeric procyanidins have been reported to possess different antioxidant capacities. However, the intracellular antioxidant mechanisms of oligomeric and polymeric procyanidins are still poorly understood. In this study, we evaluated the cytoprotective effects of the oligomeric procyanidin fraction (OPF)
Qicai Xue et al.
Chemical communications (Cambridge, England), 49(35), 3700-3702 (2013-03-29)
A new synthetic approach toward direct C-N bond formation through sp(3) C-H activation has been developed under metal-free conditions. Both primary and secondary benzylic C-H substrates could react smoothly with various amines to give only mono-amination products with good to
Yury Minko et al.
Nature protocols, 8(4), 749-754 (2013-03-23)
This protocol describes a new approach for the preparation of stereodefined trisubstituted chiral enolate species, avoiding conventional asymmetric enolization of carbonyl compounds. This protocol was developed as a single-flask synthetic sequence and therefore does not require isolation or purification of
Michael K Coggins et al.
Journal of the American Chemical Society, 135(11), 4260-4272 (2013-02-26)
Manganese-peroxos are proposed as key intermediates in a number of important biochemical and synthetic transformations. Our understanding of the structural, spectroscopic, and reactivity properties of these metastable species is limited, however, and correlations between these properties have yet to be
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