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:
Molecular Weight:
302.45
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
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Quality Level
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
SMILES string
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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Application
Polymerization Initiator
Legal Information
Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4 - Org. Perox. B
Storage Class Code
4.1A - Other explosive hazardous materials
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
[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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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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