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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號碼:
229-782-3
MDL號碼:
MFCD00084801
分類程式碼代碼:
12162002
PubChem物質ID:
24871659

品質等級

100

化驗

92%

折射率

n20/D 1.441 (lit.)

mp

≥50 °C (SADT) (lit.)

密度

0.904 g/mL at 25 °C

儲存溫度

2-8°C

SMILES 字串

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 密鑰

NALFRYPTRXKZPN-UHFFFAOYSA-N

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應用

聚合引发剂

法律資訊

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

象形圖

Exploding BombFlame
GHS01,GHS02

訊號詞

Danger

危險聲明

H241,H413

危險分類

Aquatic Chronic 4 - Org. Perox. B

儲存類別代碼

4.1A - Other explosive hazardous materials

水污染物質分類（WGK）

WGK 2

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
MKCQ9320
MKCP0167
MKCL9239
MKCJ8188
MKCG5027

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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)
Jo-Ming Tseng et al.
Journal of hazardous materials, 192(3), 1427-1436 (2011-07-26)
Over the past 30 years, the field of thermal analysis of organic peroxides has become an important issue in chemical engineering departments, safety departments, and in companies working with polymerization, petrifaction process, and so on. The contributions of thermal analysis
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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