69573-60-0 Usage
Uses
Used in Pharmaceutical Industry:
Octadecyl caffeate is used as an antioxidant agent for its ability to protect cells from oxidative damage caused by free radicals, which is crucial in the development of treatments for various diseases.
Used in Anti-inflammatory Applications:
Octadecyl caffeate is used as an anti-inflammatory agent for its potential to reduce inflammation in the body, which can be beneficial in managing inflammatory conditions.
Used in Anti-cancer Applications:
Octadecyl caffeate is used as an anti-cancer agent for its potential to inhibit the growth of certain cancer cells, offering a natural alternative or supplement to conventional cancer treatments.
Used in Neuroprotective Applications:
Octadecyl caffeate is used as a neuroprotective agent due to its potential to protect the nervous system, which can be particularly useful in the treatment of neurodegenerative diseases.
Used in Anti-aging Applications:
Octadecyl caffeate is used as an anti-aging agent for its potential to delay the aging process, which can be incorporated into skincare products or health supplements to promote longevity and maintain youthfulness.
Check Digit Verification of cas no
The CAS Registry Mumber 69573-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69573-60:
(7*6)+(6*9)+(5*5)+(4*7)+(3*3)+(2*6)+(1*0)=170
170 % 10 = 0
So 69573-60-0 is a valid CAS Registry Number.
69573-60-0Relevant academic research and scientific papers
Antioxidant properties and efficacies of synthesized alkyl caffeates, ferulates, and coumarates
Sorensen, Ann-Dorit Moltke,Jacobsen, Charlotte,Durand, Erwann,Laguerre, Mickal,Bayrasy, Christelle,Lecomte, Jrme,Villeneuve, Pierre
, p. 12553 - 12562 (2015/04/21)
Caffeic, ferulic, and coumaric acids were lipophilized with saturated fatty alcohols (C1-C20). The antioxidant properties of these hydroxycinnamic acids and their alkyl esters were evaluated in various assays. Furthermore, the antioxidant efficiency of the compounds was evaluated in a simple o/w microemulsion using the conjugated autoxidizable triene (CAT) assay. All evaluated phenolipids had radical scavenging, reducing power, and metal chelating properties. Only caffeic acid and caffeates were able to form a complex with iron via their catechol group in the phenolic ring. In the o/w emulsion, the medium chain phenolipids of the three homologues series were most efficient. The antioxidant properties and efficacies were dependent upon functional groups substituted to the ring structure and were in the following order: caffeic acid and caffeates > ferulic acid and ferulates > coumaric acid and coumarates. Moreover, the results demonstrated that the test system has an impact on the antioxidative properties measured.
