90540-32-2 Usage
Description
10-hydroperoxy-8,12-octadecadienoic acid is a C18 long-chain hydroperoxy fatty acid with E and Z double bonds at C-8 and C-12, respectively, and a hydroperoxy group at C-10.
Uses
Used in Pharmaceutical Industry:
10-hydroperoxy-8,12-octadecadienoic acid is used as a pharmaceutical agent for its potential anti-inflammatory and analgesic properties. It may be utilized in the development of drugs targeting inflammation and pain relief.
Used in Cosmetic Industry:
10-hydroperoxy-8,12-octadecadienoic acid is used as an active ingredient in cosmetics for its potential skin health benefits. It may contribute to moisturization, skin barrier function, and anti-inflammatory effects, making it suitable for skincare products.
Used in Research Applications:
10-hydroperoxy-8,12-octadecadienoic acid is used as a research compound for studying the biological effects of hydroperoxy fatty acids. It can be employed in laboratory experiments to investigate its role in cellular processes and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90540-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90540-32:
(7*9)+(6*0)+(5*5)+(4*4)+(3*0)+(2*3)+(1*2)=112
112 % 10 = 2
So 90540-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O4/c1-2-3-4-5-8-11-14-17(22-21)15-12-9-6-7-10-13-16-18(19)20/h8,11-12,15,17,21H,2-7,9-10,13-14,16H2,1H3,(H,19,20)/b11-8-,15-12+
90540-32-2Relevant articles and documents
Mechanism of lipid peroxidation photosensitized by tiaprofenic acid: Product studies using linoleic acid and 1,4-Cyclohexadienes as model substrates
Samadi, Abdelouahid,Martinez, Luis A.,Miranda, Miguel A.,Morera, Isabel M.
, p. 359 - 365 (2007/10/03)
A careful study of the linoleic acid hydroperoxide (LOOH) profile obtained upon peroxidation of linoleic acid (LA) photosensitized by tiaprofenic acid (TPA) and analogous ketones has been undertaken to distinguish between type-I and type-II photoperoxidation mechanisms. 1,4-Cyclohexadiene and 1,2-dimethylcyclohexa-2,5-diene-carboxylic acid (CHDCA) have also been used as models for LA since they also have double allylic systems. Coir-radiation of LA with TPA and decarboxytiaprofenic acid (DTPA) in acetonitrile and micellar media produced significant amounts of conjugated dienic LOOH. The cis,trans to trans,trans ratio depended on the irradiation time; thus, this parameter is an ambiguous tool for mechanistic assignment. An interesting finding was the decrease of the LOOH level after long irradiation times in mixtures photooxidized by DTPA, which is attributed to quenching of the DTPA triplet by the generated dienic LOOH. High-performance liquid chromatography analyses confirmed that the main pathway operating in photodynamic lipid peroxidation sensitized by (D)TPA is a type-I mechanism. However, product studies using CHDCA have clearly shown that a type-II mechanism is also operating and might contribute to the overall photooxidation process in a significant way.
