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290785

Sigma-Aldrich

Luperox® LP, Lauroyl peroxide

≥98%

Synonym(s):

Lauroyl peroxide, Di(dodecanoyl) peroxide, DiDodecanoyl Peroxide, Dilauroyl peroxide, Dodecanoyl peroxide

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About This Item

Linear Formula:
[CH3(CH2)10CO]2O2
CAS Number:
105-74-8
Molecular Weight:
398.62
Beilstein/REAXYS Number:
1804936
EC Number:
203-326-3
MDL number:
MFCD00008964
UNSPSC Code:
12162002
PubChem Substance ID:
24857486
NACRES:
NA.23

vapor density

13.7 (vs air)

assay

≥98%

form

solid

reaction suitability

reagent type: oxidant

mp

53-57 °C (lit.)

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC

InChI

1S/C24H46O4/c1-3-5-7-9-11-13-15-17-19-21-23(25)27-28-24(26)22-20-18-16-14-12-10-8-6-4-2/h3-22H2,1-2H3

InChI key

YIVJZNGAASQVEM-UHFFFAOYSA-N

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Application

Lauroyl peroxide can be used as:
  • A long chain branching(LCB) introducer in polypropylene to improve its mechanical recycling process.
  • A mild oxidant and efficient hydrogen abstractor in the preparation of disulfide compounds through dimerization of corresponding dithiocarbamates.
  • An initiator in the preparation of ion-imprinted polymers(IIPs).
  • An initiator and oxidant to construct erythrina ring system via oxidative radical cyclizations of enamide in the presence of nBu3SnH.

Legal Information

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

pictograms

Flame
GHS02

signalword

Danger

hcodes

H242

Hazard Classifications

Org. Perox. D

Storage Class

5.2 - Organic peroxides and self-reacting hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Saeed Kakaei et al.
Organic & biomolecular chemistry, 11(33), 5481-5490 (2013-07-17)
A series of (2-alkylthiothiazolin-5-yl)methyl dodecanoates was synthesized from various alkyl N-allylcarbamodithioates and dilauroyl peroxide via a tandem radical hydrogen-abstraction-cyclization-substitution/combination reaction with a 5-exo-trig radical cyclization as a key step. The current route is the first, convenient, and efficient synthesis of
Y Sorata et al.
Biochimica et biophysica acta, 799(3), 313-317 (1984-06-29)
Photosensitized hemolysis of human erythrocytes by hematoporphyrin was suppressed by flavonols such as quercetin and rutin at submillimolar concentrations. The suppression of photohemolysis was accompanied by inhibition of lipid peroxidation by the reagents. Quercetin and rutin were photooxidized in the
A J Klein-Szanto et al.
The Journal of investigative dermatology, 79(1), 30-34 (1982-07-01)
Free radical generating peroxides are potent skin irritants. After a single topical application of either 10, 20, or 40 mg of lauroyl peroxides or benzoyl peroxide on the dorsal skin of Sencar mice, the epidermal thickness increased markedly. No major
Itxaso Parola et al.
Polymers, 11(7) (2019-07-18)
This work reports on a diameter dependence analysis of the performance as luminescent solar concentrators of three self-fabricated polymer optical fibers (POFs) doped with a hybrid combination of dopants. The works carried out include the design and self-fabrication of the
Studies on the effect of functional monomer and porogen on the properties of ion imprinted polymers based on Cr(III)-1,10-phenanthroline complex designed for selective removal of Cr(III) ions
Laura Trzonkowska, et al.
Reactive and Functional Polymers, 117, 131-139 (2017)
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