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479896

Sigma-Aldrich

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

92%

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Synonym(s):
1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane
Linear Formula:
[(CH3)3COO]2C6H7(CH3)3
CAS Number:
6731-36-8
Molecular Weight:
302.45
EC Number:
229-782-3
MDL number:
MFCD00084801
UNSPSC Code:
12162002
PubChem Substance ID:
24871659

Quality Level

100

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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Related Categories

Application

Polymerization Initiator

Legal Information

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

Pictograms

Exploding BombFlame
GHS01,GHS02

Signal Word

Danger

Hazard Statements

H241,H413

Hazard Classifications

Aquatic Chronic 4 - Org. Perox. B

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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
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
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
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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