Dilauroyl peroxide, 97%, Thermo Scientific Chemicals
Dilauroyl peroxide, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Dilauroyl peroxide, 97%, Thermo Scientific Chemicals

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Catalog number L14310.36
also known as L14310-36
Price (USD)/ Each
110.65
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Ends: 31-Dec-2024
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Quantity:
500 g
Request bulk or custom format
Price (USD)/ Each
110.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
130.00 
Save 19.35 (15%)
Add to cart
Dilauroyl peroxide, 97%, Thermo Scientific Chemicals
Catalog numberL14310.36
Price (USD)/ Each
110.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
130.00 
Save 19.35 (15%)
-
Add to cart
Chemical Identifiers
CAS105-74-8
IUPAC Namedodecanoyl dodecaneperoxoate
Molecular FormulaC24H46O4
InChI KeyYIVJZNGAASQVEM-UHFFFAOYSA-N
SMILESCCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Appearance (Color)White
Assay from Supplier's CofA≥96.0%
FormPowder or pellets or flakes or granules
Melting Point (clear melt)53-57?C
Lauroyl peroxide acts as a bleaching agent, drying agent for fats, oils and waxes. Further, it serves as a polymerization initiator as well as vulcanizing agent. In addition to this, it plays an important role for high-pressure polyethylene and food used in bleaching agent.

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
Lauroyl peroxide acts as a bleaching agent, drying agent for fats, oils and waxes. Further, it serves as a polymerization initiator as well as vulcanizing agent. In addition to this, it plays an important role for high-pressure polyethylene and food used in bleaching agent.

Solubility
Soluble in oils and organic solvents. Slightly soluble in alcohol. Insoluble in water.

Notes
Incompatible with acids, bases, metals, reducing agents, powdered metals, strong reducing agents and combustible material.
RUO – Research Use Only

General References:

  1. Free-radical initiator. Xanthates undergo hydrodesulfurization with the reagent in refluxing isopropanol: Tetrahedron Lett., 37, 5877 (1996). The reaction has been extended to the cyclization of 3-aroylpropyl xanthates to tetralones: Tetrahedron Lett., 38, 1759 (1997); 1,2,3,4-tetrahydroisoquinolin-1-ones can be prepared similarly: Tetrahedron Lett., 39, 7295 (1998).
  2. Han, S.; Zard, S. Z. A convergent route to substituted azetidines and to Boc-protected 4-aminomethylpyrroles. Tetrahedron 2015, 71 (22), 3680-3689.
  3. Qiu, W.; Raghavanpillai, A.; Brown, P. A.; Atkinson, W. R.; Vincent, M. F.; Marshall, W. J. Ethylene-tetrafluoroethylene (ETFE) cotelomer iodides and their transformation to surface protection intermediates. J. Fluorine Chem. 2015, 169, 12-23.