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Merck
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Key Documents

추가 자료

290785

Sigma-Aldrich

Luperox® LP, Lauroyl peroxide

≥98%

동의어(들):

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

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모든 사진(4)

About This Item

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

vapor density

13.7 (vs air)

분석

≥98%

형태

solid

반응 적합성

reagent type: oxidant

mp

53-57 °C (lit.)

저장 온도

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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관련 카테고리

애플리케이션

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.

법적 정보

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

픽토그램

Flame
GHS02

신호어

Danger

유해 및 위험 성명서

H242

Hazard Classifications

Org. Perox. D

Storage Class Code

5.2 - Organic peroxides and self-reacting hazardous materials

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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

시험 성적서(COA)

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문서 라이브러리 방문

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
Lauroyl peroxide.
IARC monographs on the evaluation of carcinogenic risks to humans, 71 Pt 3, 1485-1487 (1999-09-07)
Amparo Cantó-Mirapeix et al.
Electrophoresis, 29(21), 4399-4406 (2008-10-24)
The preparation of lauryl methacrylate (LMA)-based monolithic columns for CEC using lauroyl peroxide (LPO) as thermal initiator of polymerization has been investigated. The influence of initiator amount and composition of porogenic solvent on the physical and electrochromatographic properties of the
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
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