13920-14-4 Usage
Description
15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene is a naturally occurring carotenoid, which is an intermediate in the biosynthesis of carotenoids. It is a clear, colorless oil with unique chemical properties that make it valuable in various applications.
Uses
1. Used in Pharmaceutical Industry:
15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene is used as an intermediate for the production of carotenoids, which are essential for various biological functions and have significant health benefits. These carotenoids are used in the development of pharmaceutical products that target specific health conditions.
2. Used in Nutraceutical Industry:
In the nutraceutical industry, 15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene is used as a key component in the synthesis of carotenoids that are added to dietary supplements and functional foods. These carotenoids contribute to the overall health and well-being of consumers by providing essential nutrients and supporting various physiological processes.
3. Used in Cosmetic Industry:
15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene is also utilized in the cosmetic industry as a natural colorant and antioxidant. Its clear, colorless oil form makes it an ideal ingredient for various cosmetic products, such as creams, lotions, and serums, where it helps to maintain the product's stability and enhance its appearance.
4. Used in Agricultural Industry:
In agriculture, 15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene is used as a precursor in the production of carotenoids that are essential for the natural coloration and health of plants. These carotenoids can be applied to crops to improve their nutritional value and enhance their resistance to various environmental stresses.
5. Used in Food Industry:
The food industry utilizes 15-cis-7,7',8,8',11,11',12,12'-octahydro-psi.psi-Carotene as a natural colorant and antioxidant in the production of various food products. Its clear, colorless oil form allows for easy incorporation into a wide range of products, such as beverages, snacks, and ready-to-eat meals, where it helps to maintain freshness and improve the overall quality of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 13920-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,2 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13920-14:
(7*1)+(6*3)+(5*9)+(4*2)+(3*0)+(2*1)+(1*4)=84
84 % 10 = 4
So 13920-14-4 is a valid CAS Registry Number.
13920-14-4Relevant articles and documents
POLYPRENOLS AND HYDROXYLATED LYCOPERSENES FROM MYRIOPHYLLUM VERTICILLATUM
Lanzetta, Rosa,Monaco, Pietro,Previtera, Lucio,Simaldone, Antonella
, p. 887 - 890 (1988)
Key Word Index-Myriophyllum verticillatum; Haloragaceae; terpenoids; polyprenols; hydroxy lycopersene; iso-hydroxy lycopersene.In a chemical investigation of the aquatic plant Myriophyllum verticillatum three polyprenols and two monohydroxy lycopersenes have been characterized on the basis of their chemical and physical features.The novel compounds hydroxy lycopersene and iso-hydroxy lycopersene may be easily included in the carotenoid biosynthetic pathway.
Formation of symmetrical alkenes by homocoupling of metallated sulfones under nickel catalysis
Gai, Yonghua,Julia, Marc,Jean-Noe,Verpeaux
, p. 805 - 816 (2007/10/03)
Summary -Allylic sulfones undergo a coupling reaction with organometallic compounds (Mg or Li) not only with copper catalysts but also with iron or nickel salts. With 7,7-disubstituted allylic sulfones and also saturated aliphatic sulfones, however, another reaction was observed whereby two molecules of the starting sulfone are coupled to give symmetrical alkenes. The scope of this reaction was investigated. Elsevier.
Synthese d'olefines et de polyenes par doublement d'anions α-sulfonyles en presence de sels de nickel
Julia, Marc,Verpeaux, Jean-Noel
, p. 2457 - 2460 (2007/10/02)
The lithium or magnesium derivatives of allyl, benzyl and alkyl sulphones are converted efficiently by a catalytic amount of nickel(II) acetylacetonate into symmetrical olefins in THF at 60 deg C.Thus, phytoene was obtained in a 70percent yield from geranylgeranylsulphone.