蒸汽密度
13.7 (vs air)
化驗
≥98%
形狀
solid
反應適用性
reagent type: oxidant
mp
53-57 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
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 密鑰
YIVJZNGAASQVEM-UHFFFAOYSA-N
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應用
过氧化月桂酰可用作：
- 聚丙烯中的长链分支(LCB)引入剂，以改善其机械回收工艺。
- 一种温和的氧化剂和高效的氢抽取剂，可用于通过二聚化相应的二硫代氨基甲酸盐来制备二硫化合物。
- 制备离子印迹聚合物(IIP）中的引发剂。
- 一种引发剂和氧化剂，以在nBu3SnH存在的情况下通过氧化自由基环化反应构建刺桐环系。
法律資訊
Arkema Inc. 产品
Luperox is a registered trademark of Arkema Inc.
訊號詞
Danger
危險聲明
危險分類
Org. Perox. D
儲存類別代碼
5.2 - Organic peroxides and self-reacting hazardous materials
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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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