tert-Butyl hydroperoxide, 70% aq. soln., Thermo Scientific Chemicals
tert-Butyl hydroperoxide, 70% aq. soln., Thermo Scientific Chemicals
tert-Butyl hydroperoxide, 70% aq. soln., Thermo Scientific Chemicals
tert-Butyl hydroperoxide, 70% aq. soln., Thermo Scientific Chemicals
Thermo Scientific Chemicals

tert-Butyl hydroperoxide, 70% aq. soln., Thermo Scientific Chemicals

CAS: 75-91-2 | C4H10O2 | 90.122 g/mol
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Catalog number ALFA13926.0F
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Chemical Identifiers
CAS145224-94-8
IUPAC Name4-(2-sulfonatoethyl)morpholin-4-ium
Molecular FormulaC6H13NO4S
InChI KeySXGZJKUKBWWHRA-UHFFFAOYSA-N
SMILES[O-]S(=O)(=O)CC[NH+]1CCOCC1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
CommentAll components are dissolved in UV treated 18.2 megohm-cm ± 1 water, followed by pH adjustment and filtered through 0.22 micron filter.
pH6.5 ± 0.20
FormLiquid
tert-Butyl hydroperoxide is used as an initiator for radical polymerization and in various oxidation process such as sharpless epoxidation. It is involved in osmium catalyzed vicinal hydroxylation of olefins under alkaline conditions. Furthermore, it is used in catalytic asymmetric oxidation of sulfides to sulfoxides using binaphthol as a chiral auxiliary and in the oxidation of dibenzothiophenes. It plays an important role for the introduction of peroxy groups in organic synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
tert-Butyl hydroperoxide is used as an initiator for radical polymerization and in various oxidation process such as sharpless epoxidation. It is involved in osmium catalyzed vicinal hydroxylation of olefins under alkaline conditions. Furthermore, it is used in catalytic asymmetric oxidation of sulfides to sulfoxides using binaphthol as a chiral auxiliary and in the oxidation of dibenzothiophenes. It plays an important role for the introduction of peroxy groups in organic synthesis.

Solubility
Miscible with water and diethyl ether.

Notes
Light sensitive. Store in cool place. Incompatible with powdered metals, strong oxidizing agents, reducing agents, acids, alkalis and heavy metals.
RUO – Research Use Only

General References:

  1. Li, D.; Yang, T.; Su, H.; Yu, W. tert-Butyl Hydroperoxide and Tetrabutylammonium Iodide-Promoted Free Radical Cyclization of α-Imino-N-arylamides and alfa-Azido-N-arylamides. Adv. Synth. Catal. 2015, 357 (11), 2529-2539.
  2. Sousa, C.; Moita, E.; Valentão, P.; Fernandes, F.; Monteiro, P.; Andrade, P. B. Effects of Colored and Noncolored Phenolics of Echium plantagineum L. Bee Pollen in Caco-2 Cells under Oxidative Stress Induced by tert-Butyl Hydroperoxide. J. Agric. Food. Chem. 2015, 63 (7), 2083-2091.