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Cholesterol 7-hydroperoxide is a reactive oxygen species derived from the oxidation of cholesterol, a sterol found in the cell membranes of animals. It plays a significant role in the pathogenesis of atherosclerosis, a condition characterized by the buildup of plaques in the arteries. The formation of cholesterol 7-hydroperoxide occurs when cholesterol molecules in low-density lipoproteins (LDL) are exposed to reactive oxygen species, such as superoxide anions, leading to the addition of a hydroperoxide group to the cholesterol molecule. This modification can trigger the inflammatory response and promote the formation of foam cells, which are macrophages engorged with lipids, contributing to the development of atherosclerotic lesions. Additionally, cholesterol 7-hydroperoxide can further react with other molecules, leading to the formation of more complex and potentially harmful oxidation products. Understanding the role of cholesterol 7-hydroperoxide in disease processes is crucial for the development of therapeutic strategies aimed at reducing the oxidative stress associated with cardiovascular diseases.

2846-29-9

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2846-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2846-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2846-29:
(6*2)+(5*8)+(4*4)+(3*6)+(2*2)+(1*9)=99
99 % 10 = 9
So 2846-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H46O3/c1-17(2)7-6-8-18(3)21-9-10-22-25-23(12-14-27(21,22)5)26(4)13-11-20(28)15-19(26)16-24(25)30-29/h16-18,20-25,28-29H,6-15H2,1-5H3/t18-,20+,21-,22+,23+,24-,25+,26+,27-/m1/s1

2846-29-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-hydroxycholest-5-ene-7α-hydroperoxide

1.2 Other means of identification

Product number -
Other names CHOLESTEROL-7-HYDROPEROXIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2846-29-9 SDS

2846-29-9Relevant academic research and scientific papers

Cholesterol hydroperoxides generate singlet molecular oxygen [O 2(1Δg)]: Near-IR emission, 18O-labeled hydroperoxides, and mass spectrometry

Uemi, Miriam,Ronsein, Graziella E.,Prado, Fernanda M.,Motta, Flavia D.,Miyamoto, Sayuri,Medeiros, Marisa H. G.,Di Mascio, Paolo

experimental part, p. 887 - 895 (2012/04/11)

In mammalian membranes, cholesterol is concentrated in lipid rafts. The generation of cholesterol hydroperoxides (ChOOHs) and their decomposition products induces various types of cell damage. The decomposition of some organic hydroperoxides into peroxyl

Synthesis of 7-hydroperoxycholesterol and its separation, identification, and quantification in cholesterol heated model systems

Nogueira, Gislaine C.,Costa, Bruna Z.,Crotti, Antonio E. M.,Bragagnolo, Neura

experimental part, p. 10226 - 10230 (2011/05/05)

7-Hydroperoxycholesterol is considered to be an intermediate compound of the cholesterol oxidation path as the first product formed when cholesterol is oxidized by triplet oxygen. However, there is a limitation on cholesterol mechanism studies because of the lack of 7-hydroperoxycholesterol analytical standard due to its low stability. To verify the formation of hydroperoxides in cholesterol model systems heated at 140, 180, and 220 °C, 7α-hydroperoxycholesterol was synthesized by cholesterol photooxidation followed by rearrangement at room temperature in chloroform. Its structure was confirmed on the basis of 13C NMR and mass spectra obtained by APCI-LC-MS. The synthesized compound was also used as standard for the quantification of 7-hydroperoxycholesterol as the sum of 7α-and 7β-hydroperoxycholesterol. The results demonstrated that 7-hydroperoxycholesterol is the first compound formed when the temperature is lower (140 °C). However, the concentration of the 7-hydroperoxycholesterol depends on the temperature and time of exposure: the higher the time, the higher the amount of 7-hydroperoxycholesterol at lower temperatures, and the lower the time, the lower the amount of 7-hydroperoxycholesterol at higher temperatures (180 and 220 °C). By the formation of 7-hydroperoxycholesterol, the known cholesterol oxidation mechanism in three phases (initiation, propagation, and termination) could be confirmed; once at lower temperatures, the stage of cholesterol oxidation is at initiation, at which hydroperoxide formation predominates.

Allylic oxidations catalyzed by dirhodium caprolactamate via aqueous tert-butyl hydroperoxide: The role of the tert-butylperoxy radical

McLaughlin, Emily C.,Choi, Hojae,Wang, Kan,Chiou, Grace,Doyle, Michael P.

supporting information; experimental part, p. 730 - 738 (2009/07/04)

Dirhodium(II) caprolactamate exhibits optimal efficiency for the production of the tert-butylperoxy radical, which is a selective reagent for hydrogen atom abstraction. These oxidation reactions occur with aqueous tert-butyl hydroperoxide (TBHP) without rapid hydrolysis of the caprolactamate ligands on dirhodium. Allylic oxidations of enones yield the corresponding enedione in moderate to high yields, and applications include allylic oxidations of steroidal enones. Although methylene oxidation to a ketone is more effective, methyl oxidation to a carboxylic acid can also be achieved. The superior efficiency of dirhodium(II) caprolactamate as a catalyst for allylic oxidations by TBHP (mol % of catalyst, % conversion) is described in comparative studies with other metal catalysts that are also reported to be effective for allylic oxidations. That different catalysts produce essentially the same mixture of products with the same relative yields suggests that the catalyst is not involved in product-forming steps. Mechanistic implications arising from studies of allylic oxidation with enones provide new insights into factors that control product formation. A previously undisclosed disproportionation pathway, catalyzed by the tert-butoxy radical, of mixed peroxides for the formation of ketone products via allylic oxidation has been uncovered.

Allylic Oxidations Catalyzed by Dirhodium Catalysts under Aqueous Conditions

-

Page/Page column 16-18; 20, (2009/04/24)

The present invention relates to compositions and methods for achieving the efficient allylic oxidation of organic molecules, especially olefins and steroids, under aqueous conditions. The invention concerns the use of dirhodium (II,II) “paddlewheel complexes, and in particular, dirhodium carboximate and tert-butyl hydroperoxide as catalysts for the reaction. The use of aqueous conditions is particularly advantageous in the allylic oxidation of 7-keto steroids, which could not be effectively oxidized using anhydrous methods, and in extending allylic oxidation to enamides and enol ethers.

Catalysis of Ene Reactions by Lithium Perchlorate

Davies, Alwyn G.,Kinart, Wojciech J.

, p. 2281 - 2284 (2007/10/02)

The ene reaction of some allylic hydrocarbons, and the metallo-ene reaction of some allyltin compounds, with 1,3,4-triazoline-2,5-diones or with diethyl azodicarboxylate as enophiles, in diethyl ether are strongly catalysed by lithium perchlorate.Azobenzene, on the other hand, reacts slowly with alkyltin compounds, undergoing hydrostannation.The reaction of cholesterol or of tributylallyltin with singlet oxygen is subject to a smaller catalysis.

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