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Merck
CN

479896

Luperox® 231, 1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane

92%

Synonym(s):

1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane

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About This Item

Linear Formula:
[(CH3)3COO]2C6H7(CH3)3
CAS Number:
6731-36-8
Molecular Weight:
302.45
UNSPSC Code:
12162002
PubChem Substance ID:
24871659
EC Number:
229-782-3
MDL number:
MFCD00084801

Key Documents

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Product Name

Luperox® 231, 1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, 92%

InChI key

NALFRYPTRXKZPN-UHFFFAOYSA-N

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

SMILES string

CC1CC(C)(C)CC(C1)(OOC(C)(C)C)OOC(C)(C)C

assay

92%

refractive index

n20/D 1.441 (lit.)

mp

≥50 °C (SADT) (lit.)

density

0.904 g/mL at 25 °C

storage temp.

2-8°C

Quality Level

100

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Legal Information

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

Application

Polymerization Initiator

pictograms

Exploding BombFlame
GHS01,GHS02

signalword

Danger

hcodes

H241,H413

Hazard Classifications

Aquatic Chronic 4 - Org. Perox. B

Storage Class

4.1A - Other explosive hazardous materials

wgk

WGK 2

ppe

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9067
MKCX1372
MKCT0824
MKCP0167
MKCS6688

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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
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
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
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