159042
Luperox®P,叔-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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线性分子式:
C6H5COOOC(CH3)3
化学文摘社编号:
分子量:
194.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-382-2
Beilstein/REAXYS Number:
1342734
MDL number:
产品名称
Luperox®P,叔-过氧苯甲酸丁酯, 98%
InChI key
GJBRNHKUVLOCEB-UHFFFAOYSA-N
InChI
1S/C11H14O3/c1-11(2,3)14-13-10(12)9-7-5-4-6-8-9/h4-8H,1-3H3
SMILES string
CC(C)(C)OOC(=O)c1ccccc1
vapor density
6.7 (vs air)
vapor pressure
3.36 mmHg ( 50 °C)
assay
98%
form
liquid
refractive index
n20/D 1.499 (lit.)
bp
75-76 °C/0.2 mmHg (lit.)
solubility
water: soluble 1.18 g/L
density
1.021 g/mL at 25 °C (lit.)
functional group
peroxide
phenyl
Quality Level
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Application
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
General description
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。
Legal Information
Arkema Inc. 产品
Luperox is a registered trademark of Arkema Inc.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 3 - Org. Perox. C - Skin Irrit. 2 - Skin Sens. 1
存储类别
4.1A - Other explosive hazardous materials
wgk
WGK 2
flash_point_f
200.1 °F - closed cup
flash_point_c
93.4 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Jingjing Xu et al.
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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
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)
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)
Margaret Hanausek et al.
Carcinogenesis, 25(3), 431-437 (2003-11-25)
Screening of newly synthesized organic peroxides for tumor initiating/promoting activity would be greatly facilitated if predictive methodologies could be developed using topical exposures shorter than those required for definitive tumor assessment in mouse skin models. Nine organic peroxides [benzoyl peroxide
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