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Key Documents

479896

Sigma-Aldrich

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

92%

Sinonimo/i:

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

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About This Item

Formula condensata:
[(CH3)3COO]2C6H7(CH3)3
Numero CAS:
Peso molecolare:
302.45
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:

Livello qualitativo

Saggio

92%

Indice di rifrazione

n20/D 1.441 (lit.)

Punto di fusione

≥50 °C (SADT) (lit.)

Densità

0.904 g/mL at 25 °C

Temperatura di conservazione

2-8°C

Stringa SMILE

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
NALFRYPTRXKZPN-UHFFFAOYSA-N

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Applicazioni

Polymerization Initiator

Note legali

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

Pittogrammi

Exploding BombFlame

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Aquatic Chronic 4 - Org. Perox. B

Codice della classe di stoccaggio

4.1A - Other explosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Dispositivi di protezione individuale

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


Certificati d'analisi (COA)

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[Extraction-photometric analysis of low levels of hem-ditret-butylperoxy-3,3,5-trimethylcyclohexane peroxide in in water solutions].
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Gigiena i sanitariia, (8)(8), 90-91 (1990-08-01)
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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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