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479896

Sigma-Aldrich

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

92%

Sinônimo(s):

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

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About This Item

Fórmula linear:
[(CH3)3COO]2C6H7(CH3)3
Número CAS:
6731-36-8
Peso molecular:
302.45
Número CE:
229-782-3
Número MDL:
MFCD00084801
Código UNSPSC:
12162002
ID de substância PubChem:
24871659

Ensaio

92%

índice de refração

n20/D 1.441 (lit.)

pf

≥50 °C (SADT) (lit.)

densidade

0.904 g/mL at 25 °C

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

NALFRYPTRXKZPN-UHFFFAOYSA-N

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Aplicação

Polymerization Initiator

Informações legais

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

Pictogramas

Exploding BombFlame
GHS01,GHS02

Palavra indicadora

Danger

Frases de perigo

H241,H413

Classificações de perigo

Aquatic Chronic 4 - Org. Perox. B

Código de classe de armazenamento

4.1A - Other explosive hazardous materials

Classe de risco de água (WGK)

WGK 2

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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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
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
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
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
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