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Merck
CN
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安全信息

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

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

法规信息

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分析证书(COA)

Lot/Batch Number
MKCX1372
MKCT0824
MKCP0167
MKCS6688
MKCQ9320

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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
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
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
V S Trubetskoy et al.
Bioconjugate chemistry, 10(4), 624-628 (1999-07-20)
The assembly of DNA into compact particles that do not aggregate in physiologic salt solution occurs naturally in chromatin and viral particles but has been challenging to duplicate using artificial constructs. Cross-linking amino-containing polycations in the presence of DNA with
[Extraction-photometric analysis of low levels of hem-ditret-butylperoxy-3,3,5-trimethylcyclohexane peroxide in in water solutions].
E M Sevost'ianova et al.
Gigiena i sanitariia, (8)(8), 90-91 (1990-08-01)
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