479896
Luperox® 231，1,1-双（叔丁基过氧）-3,3,5-三甲基环己烷
92%
别名:
1,1-二(叔丁基过氧)-3,3,5-三甲基环己烷
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关于此项目
线性分子式:
[(CH3)3COO]2C6H7(CH3)3
化学文摘社编号:
分子量:
302.45
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:
质量水平
方案
92%
折射率
n20/D 1.441 (lit.)
mp
≥50 °C (SADT) (lit.)
密度
0.904 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
CC1CC(C)(C)CC(C1)(OOC(C)(C)C)OOC(C)(C)C
InChI
1S/C17H34O4/c1-13-10-16(8,9)12-17(11-13,20-18-14(2,3)4)21-19-15(5,6)7/h13H,10-12H2,1-9H3
InChI key
NALFRYPTRXKZPN-UHFFFAOYSA-N
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应用
聚合引发剂
法律信息
Arkema Inc. 产品
Luperox is a registered trademark of Arkema Inc.
警示用语：
Danger
危险声明
危险分类
Aquatic Chronic 4 - Org. Perox. B
储存分类代码
4.1A - Other explosive hazardous materials
WGK
WGK 2
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
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Xiaopeng Shan et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(15), 5340-5345 (2005-04-02)
The reaction of [Fe(2)(mu-OH)(2)(6-Me(3)-TPA)(2)](2+) (1) [6-Me(3)-TPA, Tris(6-methyl-2-pyridylmethyl)amine] with O(2) in CH(2)Cl(2) at -80 degrees C gives rise to two new intermediates, 2 and 3, before the formation of previously characterized [Fe(2)(O)(O(2))(6-Me(3)-TPA)(2)](2+) (4) that allow the oxygenation reaction to be monitored
M Mitsui et al.
Eisei Shikenjo hokoku. Bulletin of National Institute of Hygienic Sciences, (110)(110), 42-48 (1992-01-01)
A 13-week subchronic toxicity study of 1,1-bis(t-butylperoxy)3,3,5-trimethyl cyclohexane (TMCH) was performed in male and female B6C3F1 mice by feeding a CRF-1 powder diet containing 0, 0.5, 1.0, 2.0 and 4.0% TMCH, to determine the maximum tolerable dose (MTD) for subsequent
M Mitsui et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 31(12), 929-933 (1993-12-01)
1,1-Bis(tert-butylperoxy)-3.3.5-trimethylcyclohexane (BBTC) is widely used in the manufacture of rubber. The present carcinogenicity study in B6C3F1 mice was carried out in order to assess its potential to induce tumours. BBTC was administered at dietary levels of 0 (control), 0.25 and
O I Shadyro et al.
Voprosy meditsinskoi khimii, 43(3), 153-157 (1997-05-01)
The bioantioxidant activity of the synthesized by us on the base of the diatomic phenol compound--3,5-di-t-butylpyrocatechol--has been studied. It was shown that this substance exhibits more pronounced antioxidant properties than tocopherol on the lipid peroxidation process in the rat brain
Fabrication and characterization of DTBP-crosslinked chitosan scaffolds for skin tissue engineering.
Iyabo Adekogbe et al.
Biomaterials, 26(35), 7241-7250 (2005-07-14)
Chitosan, the deacetylated derivative of chitin, is a promising scaffold material for skin tissue engineering applications. It is biocompatible and biodegradable, and the degradation products are resorbable. However, the rapid degradation of chitosan and its low mechanical strength are concerns
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