Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
[(CH3)3COO]2C6H7(CH3)3
CAS Number:
Molecular Weight:
302.45
UNSPSC Code:
12162002
PubChem Substance ID:
EC Number:
229-782-3
MDL number:
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
Application
Polymerization Initiator
Legal Information
Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.
signalword
Danger
hcodes
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
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Fabrication and characterization of DTBP-crosslinked chitosan scaffolds for skin tissue engineering.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 479896-500ML | 04061832373447 |

