493015-74-0 Usage
Uses
Used in Pharmaceutical Industry:
Pinolenic Acid ethyl ester is used as a bioactive compound for its potential therapeutic effects. It is derived from pine nuts, which are known to have various health benefits, and the ester form may enhance its bioavailability and efficacy in pharmaceutical applications.
Used in Nutritional Supplements:
Pinolenic Acid ethyl ester is used as an ingredient in nutritional supplements for its potential health-promoting properties. The ester form may improve the absorption and utilization of the compound in the body, providing enhanced benefits compared to the free acid form.
Used in Food Industry:
Pinolenic Acid ethyl ester is used as an additive in the food industry to enhance the nutritional value and health benefits of certain products. Its presence in pine nuts, which are considered a healthy food source, makes it a desirable component for the development of functional foods.
Used in Cosmetics Industry:
Pinolenic Acid ethyl ester is used as an ingredient in cosmetics for its potential skin health benefits. The ester form may provide improved stability and bioavailability, making it a valuable component in skincare products.
Check Digit Verification of cas no
The CAS Registry Mumber 493015-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,3,0,1 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 493015-74:
(8*4)+(7*9)+(6*3)+(5*0)+(4*1)+(3*5)+(2*7)+(1*4)=150
150 % 10 = 0
So 493015-74-0 is a valid CAS Registry Number.
493015-74-0Relevant academic research and scientific papers
Kaltia, Seppo,Matikainen, Jorma,Ala-Peijari, Maija,Hase, Tapio
, p. 561 - 565 (2008)
Pinolenic acid (5Z,9Z,12Z-octadecatrienoic acid, 1a), one of the most abundant trienoic fatty acids in nature, is very difficult to obtain in quantity in a pure state from the highly complex mixture of unsaturated tall oil fatty acids. For this reason its chemistry has been little studied when compared to linolenic or linoleic acids. A simple synthesis of esters of 1a and of 12Z,15Z-octadecadienoic acid 3 using the one pot double Wittig procedure is described here. The products of double Wittig reactions were purified by argentation chromatography, and their structural purity was established by 1H-, 13C-NMR and 2D-NMR spectroscopies.
