68124-68-5 Usage
Uses
Used in Surfactant and Emulsifier Applications:
Trimethyl[2-[[oxido[(2-pentadecyl-1,3-dioxolan-4-yl)methoxy]phosphinyl]oxy]ethyl]ammonium is used as a surfactant and emulsifier in various industrial and household products due to its ability to reduce surface tension and stabilize mixtures of oil and water.
Used in Disinfectant and Antimicrobial Applications:
In the field of disinfection and antimicrobial agents, trimethyl[2-[[oxido[(2-pentadecyl-1,3-dioxolan-4-yl)methoxy]phosphinyl]oxy]ethyl]ammonium serves as an effective agent for killing bacteria and other pathogens, leveraging its cationic nature to disrupt microbial cell membranes.
Used in Skincare and Hair Care Products:
Trimethyl[2-[[oxido[(2-pentadecyl-1,3-dioxolan-4-yl)methoxy]phosphinyl]oxy]ethyl]ammonium is used in skincare and hair care products as an ingredient that enhances the cleansing and conditioning abilities of these formulations, thanks to its amphiphilic properties that allow it to interact with both water and oils on the skin or hair.
Used in Chemical and Personal Care Industries:
trimethyl[2-[[oxido[(2-pentadecyl-1,3-dioxolan-4-yl)methoxy]phosphinyl]oxy]ethyl]ammonium is widely used across the chemical and personal care industries for its high solubility in water and compatibility with a range of other ingredients, making it a valuable component in the development of diverse products.
Check Digit Verification of cas no
The CAS Registry Mumber 68124-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,2 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68124-68:
(7*6)+(6*8)+(5*1)+(4*2)+(3*4)+(2*6)+(1*8)=135
135 % 10 = 5
So 68124-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H50NO6P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24-28-21-23(31-24)22-30-32(26,27)29-20-19-25(2,3)4/h23-24H,5-22H2,1-4H3
68124-68-5Relevant academic research and scientific papers
Preparation of optically pure 4-(hydroxymethyl)-2-pentadecyl-1,3-dioxolanes and their corresponding phosphodiester ether lipid derivatives
Lin, Sonyuan,Duclos Jr., Richard I,Makriyannis, Alexandros
, p. 111 - 122 (2007/10/03)
Semi-preparative HPLC on a chiral stationary phase (Chiracel OD) was utilized in the course of this synthesis to separate the four possible diastereomers [cis-(2R,4S)-2a, trans-(2S,4S)-2b, cis-(2S,4R)-2a′, and trans-(2R,4R)-2b′] of a 2,4-disubstituted-1,3
Darmstoff Analogues. 3. Actions of Choline Esters of Acetal Phosphatidic Acids on Visceral Smooth Muscle
Marx, Michael H.,Wiley, Robert A.,Satchell, D. G.,Maguire, M. Helen
, p. 1319 - 1322 (2007/10/02)
A number of naturally occurring phospholipids, e.g. the acetal phosphatidic acid derivatives that comprise Darmstoff (1) and the phosphatidylcholine derivative platelet activating factor (PAF), cause contraction of certain visceral smooth muscles and cause platelet activation.Because the Darmstoff phosphatidic acids and PAF are structurally similar, it was of interest to compare the biological actions of choline esters of Darmstoff with those of PAF and of the parent Darmstoff phosphatidic acids.To this end, phosphocholine (3a), methyl>phosphocholine (3b), and methyl>phosphocholine (3c) were synthesized.Compounds 3a, 3b, 3c, and PAF caused dose-dependent relaxation of taenia coli strips.In contrast, the unesterified materials 1a and 1b, as well as lyso-PAF, caused contraction in taenia coli strips.Thus, the contractile effect of Darmstoff is reversed on esterification with choline.In preparations of whole trachea, both 1a and 3a had contractile effects similar to those of PAF.
