50451-63-3 Usage
Structure
2,2,7,7,12,12,17,17-octamethyl-21,22,23,24-tetraoxapentacyclo[16.2.1.1~3,6~.1~8,11~.1~13,16~]tetracosane Squalane has a complex cyclic structure with five interconnected rings and eight methyl groups attached to the carbon skeleton.
Source
Shark liver oil or plant sources Squalane can be derived from natural sources such as shark liver oil or obtained from plants like olives and sugarcane.
Physical properties
Colorless, odorless, and non-toxic liquid Squalane is a clear, tasteless, and safe liquid that is easy to incorporate into various products.
Saturation
Saturated and branched hydrocarbon Squalane is a saturated hydrocarbon, meaning it contains only single bonds between carbon atoms and has no double bonds or unsaturated functional groups.
Uses in skincare and cosmetics
Emollient and moisturizing properties Squalane is commonly used in skincare and cosmetic products due to its ability to soften and hydrate the skin, as well as its non-comedogenic nature, which means it won't clog pores.
Lubricant
Industrial applications Squalane can be used as a lubricant in various industrial settings due to its slippery texture and non-toxic nature.
Drug delivery system
Carrier Squalane can be used as a carrier for drug delivery systems, helping to transport active ingredients to targeted areas in the body.
Safety and effectiveness
Considered safe and effective Squalane is widely recognized as a safe and effective ingredient in personal care products, with a variety of uses due to its desirable chemical and physical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 50451-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,5 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50451-63:
(7*5)+(6*0)+(5*4)+(4*5)+(3*1)+(2*6)+(1*3)=93
93 % 10 = 3
So 50451-63-3 is a valid CAS Registry Number.
50451-63-3Relevant academic research and scientific papers
Role of Metal Salts in the Synthesis of Furan-Ketone Condensation Macrocycles: An 'Apparent' Metal Template Effect
Healy, Maria de Sousa,Rest, Antony J.
, p. 973 - 982 (2007/10/02)
The acid-catalysed condensation of furan and acetone has been investigated by systematically varying the parameters of the reaction.The dramatic yield enhancement for macrocycles found on adding metal salts, and hitherto assumed to be due to a metal ion template effect, has now been demonstrated to result from pH effects.Optimisation of condensation reaction conditions has enabled a number of tetrameric furan-ketone macrocycles to be synthesized with improved yields and a tetrameric furan-cyclohaxanone macrocycle has been synthesized in a one-step reaction for the first time.Hexameric and octameric furan-acetone macrocycles have also been prepared.The tetrameric furan-ketone macrocycles show no binding interaction with any metal ion but the tetrameric tetrahydrofuran-acetone macrocycle binds strongly enough with LiClO4 to form an isolable 1:1 complex and gives very strongly perturbed 1H n.m.r. spectra in the cases of LiSCN and Ni(ClO4)2*6H2O.Increasing the number of donor sites, as in the hexameric furan-acetone and hexameric tetrahydrofuran-acetone macrocycle, did not lead to complexation of metal ions.
