3131-67-7 Usage
Uses
Used in Research and Studies:
LINOLENIC ACID, [9,12,15-1-14C] is used as a research tool for tracking the metabolism and distribution of linolenic acid in various biological systems. It aids in understanding the absorption, transportation, and metabolic pathways of omega-3 fatty acids in the human body.
Used in Human Health and Disease Studies:
This radioactive form of linolenic acid is utilized in experiments focused on elucidating the role of omega-3 fatty acids in human health and disease. It helps in identifying the mechanisms by which these essential nutrients contribute to health benefits and potentially mitigate disease risks.
Used in Pharmaceutical and Nutraceutical Development:
LINOLENIC ACID, [9,12,15-1-14C] is employed in the development of pharmaceutical and nutraceutical products, where its radioactive properties allow for the assessment of the bioavailability and efficacy of omega-3 supplements and formulations.
Used in Nutritional Science:
In the field of nutritional science, LINOLENIC ACID, [9,12,15-1-14C] is used as a tracer to study the dietary intake and metabolism of omega-3 fatty acids, providing valuable data on their role in maintaining optimal health and preventing nutritional deficiencies.
Used in Clinical Trials:
This radioactive compound is utilized in clinical trials to evaluate the effectiveness of omega-3 supplementation in treating various health conditions, such as cardiovascular diseases, inflammatory disorders, and cognitive decline.
Used in Food Science and Technology:
In food science and technology, LINOLENIC ACID, [9,12,15-1-14C] is applied to investigate the impact of food processing and cooking methods on the stability and bioavailability of omega-3 fatty acids in various food products.
Used in Agricultural Research:
This radioactive form of linolenic acid is also used in agricultural research to study the biosynthesis and accumulation of omega-3 fatty acids in plants, with the aim of developing crop varieties with enhanced nutritional value.
Check Digit Verification of cas no
The CAS Registry Mumber 3131-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3131-67:
(6*3)+(5*1)+(4*3)+(3*1)+(2*6)+(1*7)=57
57 % 10 = 7
So 3131-67-7 is a valid CAS Registry Number.
3131-67-7Relevant academic research and scientific papers
A divergent synthesis of [1-14C]-mono-E isomers of fatty acids
Georgin,Taran,Mioskowski
, p. 83 - 91 (2007/10/03)
A convenient synthesis of [1-14C]-mono-trans fatty acid using olefin inversion as a key-step is described. This methodology allows for a facile synthesis of [1-14C]-labelled mono-trans analogues of oleic, linoleic and linolenic acids. As an example, only eleven steps were necessary to obtain the [1-14C]-mono-E isomers of linolenic acid from its commercial all-Z form. In the first step, Barton's decarboxylation procedure yielded a bromo intermediate. Epoxidation of this compound resulted in the formation of three monoepoxides, which could be separated by HPLC. After identification by 1H NMR and MS, the pure monoepoxides were then subjected to inversion consisting of a stereospecific deoxygenation followed by a β-elimination step. Finally, the labelling was introduced by substitution of the bromine by a [14C]-cyano group followed by hydrolysis.
Synthesis of (9Z,12Z,15E)- and (9E,12Z,15Z)-octadecatrienoic acids and their -radiolabelled analogs
Eynard, Thierry,Vatele, Jean-Michel,Poullain, Didier,Noeel, Jean-Pierre,Chardigny, Jean-Michel,Sebedio, Jean-Louis
, p. 175 - 184 (2007/10/02)
In order to study the effect of the double bonds geometry of linolenic acid (18:3 n-3) on its biological activities, (9Z,12Z,15E)- and (9E,12Z,15Z)-octadecatrienoic acids, found in many refined vegetable oils, were made by total synthesis. Synthesis of 18
