13832-70-7 Usage
Description
Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate is a complex organic compound derived from oleanolic acid, a naturally occurring triterpenoid. It is characterized by its unique chemical structure, which includes a hydroxyl group, a carbonyl group, and an ester linkage. Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate has been found to possess various biological activities, making it a potential candidate for pharmaceutical and cosmetic applications.
Uses
Used in Pharmaceutical Applications:
Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate is used as an anti-inflammatory agent for its ability to soothe and reduce inflammation in the body. Its chemical structure allows for improved penetration and bioavailability, enhancing its therapeutic effects.
Used in Cosmetic Applications:
In the cosmetic industry, Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate is used as a key ingredient in various skincare products due to its anti-inflammatory and soothing properties. It helps to improve skin health and appearance by reducing redness, irritation, and inflammation.
Used in Drug Delivery Systems:
Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate can be utilized in the development of modified liposomes and other drug delivery systems. These systems can be loaded with various therapeutic agents, such as norcantharidin and 10-hydroxycamptothecin, for targeted cancer therapy. The unique properties of this compound allow for improved drug delivery, bioavailability, and therapeutic outcomes.
General Description:
Octadecyl 3-hydroxy-11-oxoolean-12-en-29-oate is a stearic acid ester of oleanolic acid, which is commonly found in various plant sources. It is generally used as an active ingredient in pharmaceutical and cosmetic products due to its diverse biological activities and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13832-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13832-70:
(7*1)+(6*3)+(5*8)+(4*3)+(3*2)+(2*7)+(1*0)=97
97 % 10 = 7
So 13832-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C48H82O4/c1-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-33-52-42(51)45(5)30-29-44(4)31-32-47(7)36(37(44)35-45)34-38(49)41-46(6)27-26-40(50)43(2,3)39(46)25-28-48(41,47)8/h34,37,39-41,50H,9-33,35H2,1-8H3/t37-,39-,40-,41+,44+,45-,46-,47+,48+/m0/s1
13832-70-7Relevant articles and documents
Method for synthesizing octadecyl glycyrrhetinate
-
Page/Page column 5-6, (2020/05/14)
The invention discloses a method for synthesizing octadecyl glycyrrhetinate. The method comprises the following steps of: 1, synthesizing eutectic ionic liquid by taking choline chloride and urea as raw materials; 2, dissolving alkali in water to form an alkaline solution, mixing an alkaline solution with ethanol, and adding the mixture into the eutectic ionic liquid, adding glycyrrhetinic acid, and performing reacting to obtain glycyrrhetinic acid sodium salt; 3, adding bromo-octadecane into the sodium glycyrrhetinate, carrying out primary reflux reaction under a stirring condition, performing filtering, taking filtrate, cooling to room temperature, and performing filtering to obtain an octadecyl glycyrrhetinate crude product; and 4, sequentially carrying out secondary reflux refining, filtering and reduced pressure drying on the crude product of octadecyl glycyrrhetinate to obtain octadecyl glycyrrhetinate. The method has the advantages of mild reaction conditions, simpleness and convenience in purification treatment by taking ethanol as a solvent, low energy consumption and the high yield.
