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479896

Sigma-Aldrich

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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About This Item

线性分子式:
[(CH3)3COO]2C6H7(CH3)3
CAS号:
6731-36-8
分子量:
302.45
EC 号:
229-782-3
MDL编号:
MFCD00084801
UNSPSC代码:
12162002
PubChem化学物质编号:
24871659
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质量水平

100

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.

象形图

Exploding BombFlame
GHS01,GHS02

警示用语：

Danger

危险声明

H241,H413

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCX1372
MKCT0824
MKCP0167
MKCS6688
MKCQ9320

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Sigma-Aldrich

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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
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
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
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
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