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Merck
CN

159042

Sigma-Aldrich

Luperox®P,-过氧苯甲酸丁酯

98%

别名:

过氧化苯甲酸叔丁酯, 过氧化叔丁基苯甲酸酯

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关于此项目

线性分子式:
C6H5COOOC(CH3)3
CAS Number:
分子量:
194.23
Beilstein:
1342734
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度

6.7 (vs air)

质量水平

蒸汽压

3.36 mmHg ( 50 °C)

方案

98%

表单

liquid

折射率

n20/D 1.499 (lit.)

沸点

75-76 °C/0.2 mmHg (lit.)

溶解性

water: soluble 1.18 g/L

密度

1.021 g/mL at 25 °C (lit.)

官能团

peroxide
phenyl

SMILES字符串

CC(C)(C)OOC(=O)c1ccccc1

InChI

1S/C11H14O3/c1-11(2,3)14-13-10(12)9-7-5-4-6-8-9/h4-8H,1-3H3

InChI key

GJBRNHKUVLOCEB-UHFFFAOYSA-N

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一般描述

报道了过氧化苯甲酸特丁酯(TBPB)-介导的2-异氰基二芳基插入1,4-二氧六环。

应用

氧化苯甲酸叔丁酯用作聚合和交联催化剂。它还在以下期间用作引发剂:
  • 2,2,6,6-四甲基-1-哌啶氧基(TEMPO)-4-氧乙酰胺基-(3-丙基三乙氧基硅烷)接枝到聚(乙烯共聚辛烯)上
  • 通过起始化学气相沉积制备共形聚(甲基丙烯酸环己酯)薄膜

法律信息

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

警示用语:

Danger

危险分类

Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 3 - Org. Perox. C - Skin Irrit. 2 - Skin Sens. 1

储存分类代码

4.1A - Other explosive hazardous materials

WGK

WGK 2

闪点(°F)

200.1 °F - closed cup

闪点(°C)

93.4 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jia-Jia Cao et al.
Chemical communications (Cambridge, England), 50(49), 6439-6442 (2014-04-05)
An efficient method for the construction of 6-alkyl phenanthridines by tert-butyl peroxybenzoate (TBPB)-mediated 2-isocyanobiaryl insertion with 1,4-dioxane was established. Two new C-C bonds were formed in this reaction via a sequential C(sp(3))-H/C(sp(2))-H bond functionalization under metal-free conditions.
Structural comparison of products from peroxide-initiated grafting of vinylsilane and silane-functionalized nitroxyl to hydrocarbon and polyolefin substrates.
Weaver JD, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(13), 4542-4555 (2008)
Chengguo Liu et al.
Polymers, 11(5) (2019-05-10)
New tung oil (TO)-based, unsaturated, co-ester (Co-UE) macromonomers bearing steric hindrance were synthesized by modifying a TO-based maleate (TOPERMA) monomer with an anhydride structure with hydroxyethyl methacrylate (HEMA) and methallyl alcohol (MAA), respectively. The obtained Co-UE monomers (TOPERMA-HEMA and TOPERMA-MAA)
Jingjing Xu et al.
ACS applied materials & interfaces, 3(7), 2410-2416 (2011-06-08)
Conformal poly(cyclohexyl methacrylate) (pCHMA) thin films were synthesized via initiated chemical vapor deposition (iCVD), with tert-butyl peroxybenzoate (TBPOB) as the initiator, representing the first time that TBPOB has been used as an initiator for iCVD synthesis. Using TBPOB instead of
M Athar et al.
Carcinogenesis, 10(8), 1499-1503 (1989-08-01)
Humans are exposed to various peroxy and hydroperoxy compounds which are in use in the cosmetic, pharmaceutical and polymer industries and which are also generated as a result of the peroxidative metabolic conversion of certain lipids. This study was designed

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