5502-94-3 Usage
Description
12-METHYLTETRADECANOIC ACID, also known as an anteiso-C(15)-fatty acid, is a branched-chain saturated fatty acid derived from tetradecanoic acid with a 12-methyl substituent. It is characterized by its unique structure and properties, making it a subject of interest in various scientific studies.
Uses
Used in Chemical and Pharmaceutical Research:
12-METHYLTETRADECANOIC ACID is used as a research compound for studying the properties and functions of medium-chain anteiso-fatty acids. Its unique structure and characteristics contribute to a better understanding of the behavior and potential applications of similar compounds in the chemical and pharmaceutical industries.
Used in Biomedical Applications:
In the biomedical field, 12-METHYLTETRADECANOIC ACID may be utilized as a component in the development of novel drugs or therapies targeting specific health conditions. Its unique properties could potentially be harnessed to improve drug delivery, bioavailability, and therapeutic outcomes.
Used in Industrial Applications:
12-METHYLTETRADECANOIC ACID may also find applications in various industrial processes, such as the production of specialty chemicals, lubricants, or additives, where its unique properties can provide advantages over traditional materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5502-94-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5502-94:
(6*5)+(5*5)+(4*0)+(3*2)+(2*9)+(1*4)=83
83 % 10 = 3
So 5502-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-3-14(2)12-10-8-6-4-5-7-9-11-13-15(16)17/h14H,3-13H2,1-2H3,(H,16,17)
5502-94-3Relevant articles and documents
Synthesis of (S)-(+)-enantiomers of food-relevant (n-5)-monoenoic and saturated anteiso-fatty acids by a Wittig reaction
Thurnhofer, Saskia,Vetter, Walter
, p. 1140 - 1145 (2007/10/03)
We developed an enantioselective synthesis for the food-relevant anteiso-fatty acids a15:0, a16:0, and a17:0. Different (carboxyalkyl)triphenylphosphonium bromide salts were coupled with (S)-3-methylpentanal in a Wittig reaction. Mixtures of the obtained cis-/trans-isomers were separated by Ag+-HPLC to give the novel cis-isomers of (S)-(+)-a15:1n-5, (S)-(+)-a16:1n-5, and (S)-(+)-a17:1n-5. Hydrogenation of the monoenoic products led to (S)-(+)-a15:0, (S)-(+)-a16:0, and (S)-(+)-a17:0, which are essential for the assessment of the bioactivity of tests with standards of anteiso-fatty acids.
Anticancer effects of specific branched-chain fatty acids and related production process
-
, (2008/06/13)
A group of specific branched-chain fatty acids, with significant anticancer effects on human and animals; methods of making using either chemical synthesis or biosynthesis methods; and methods of treating cancer.
1-O-(13-Methyl-1-Z-tetradecenyl)-2-O-(13-methyltetradecanoyl)-glycero-3-phospho-ethanolamine, a Plasmalogen from Myxococcus stipitatus
Stein, J.,Budzikiewicz, H.
, p. 1017 - 1020 (2007/10/02)
The structure of 1-O-(13-methyl-1-Z-tetradecenyl)-2-O-(13-methyltetradecanoyl)-glycero-3-phospho-ethanolamine isolated from Myxococcus stipitatus has been elucidated. 1H and 13C NMR as well as mass spectral data have been accumulated which allow a ready identification and structure elucidation of compounds of this type. - Keywords: Myxobacteria, Myxococcus stipitatus, Phospholipids, Plasmalogen, Structure Elucidation
