Octaethylene Glycol Monododecyl Ether
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Octaethylene Glycol Monododecyl Ether
, Section2= {{Chembox Properties , Formula=C28H58O9 , MolarMass=538.75472 , Appearance= , Density= , MeltingPt= , BoilingPt= , Solubility= , CMC =8×10−5 M at 25 °C.{{cite journal , author1=Calum J. Drummond , author2=Gregory G. Warr , author3=Franz Grieser , author4=Barry W. Ninham , author5=D. Fennel Evans , name-list-style=amp , journal = J. Phys. Chem. , title = Surface Properties and Micellar Interfacial Microenvironment of n-Dodecyl beta-d-Maitoside , year = 1985 , volume = 89 , issue = 10 , pages = 2103–2109 , doi = 10.1021/j100256a060 , HLB = , Section3= {{Chembox Hazards , MainHazards= , FlashPt= , AutoignitionPt= Octaethylene glycol monododecyl ether (C12E8) is a nonionic surfactant formed by the ethoxylation of dodecanol (lauryl alcohol) to give a material with 8 repeat units of ethylene glycol Ethylene glycol ( IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol) with the formula . It is mainly used for two purposes, as a ...
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Nonionic Surfactant
Surfactants are chemical compounds that decrease the surface tension between two liquids, between a gas and a liquid, or interfacial tension between a liquid and a solid. Surfactants may act as detergents, wetting agents, emulsifiers, foaming agents, or dispersants. The word "surfactant" is a blend of ''surface-active agent'', coined . Agents that increase surface tension are "surface active" in the literal sense but are not called surfactants as their effect is opposite to the common meaning. A common example of surface tension increase is salting out: by adding an inorganic salt to an aqueous solution of a weakly polar substance, the substance will precipitate. The substance may itself be a surfactant – this is one of the reasons why many surfactants are ineffective in sea water. Composition and structure Surfactants are usually organic compounds that are amphiphilic, meaning each molecule contains both a hydrophilic "water-seeking" group (the ''head''), and a hy ...
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Ethoxylation
Ethoxylation is a chemical reaction in which ethylene oxide adds to a substrate. It is the most widely practiced alkoxylation, which involves the addition of epoxides to substrates. In the usual application, alcohols and phenols are converted into R(OC2H4)nOH where n ranges from 1 to 10. Such compounds are called alcohol ethoxylates. Alcohol ethoxylates are often converted to related species called ethoxysulfates. Alcohol ethoxylates and ethoxysulfates are surfactants, used widely in cosmetic and other commercial products. The process is of great industrial significance with more than 2,000,000 metric tons of various ethoxylates produced worldwide in 1994. Production The process was developed at the Ludwigshafen laboratories of IG Farben by Conrad Schöller and during the 1930s. Alcohol ethoxylates Industrial ethoxylation is primarily performed upon fatty alcohols in order to generate fatty alcohol ethoxylates (FAE's), which are a common form of nonionic surfactant (e.g. octa ...
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Dodecanol
Dodecanol , or lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil. It is a fatty alcohol. Sulfate esters of lauryl alcohol, especially sodium lauryl sulfate, are very widely used as surfactants. Sodium lauryl sulfate, ammonium lauryl sulfate, and sodium laureth sulfate are all used in shampoos. Lauryl alcohol is tasteless and colorless with a floral odor. Production and use In 1993, the European demand of dodecanol was around 60 thousand tons per year (Tt/a). It can be obtained from palm kernel or coconut oil fatty acids and methyl esters by hydrogenation. It may also be produced synthetically via the Ziegler process. A classic laboratory method involves Bouveault-Blanc reduction of ethyl laurate. Dodecanol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive. In cosmetics, dodecanol is used as an emollient. It is also the precursor t ...
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Repeat Unit
In polymer chemistry, a repeat unit or repeating unit (or mer) is a part of a polymer whose repetition would produce the complete polymer chain (except for the end-groups) by linking the repeat units together successively along the chain, like the beads of a necklace. A repeat unit is sometimes called a mer (or mer unit). "Mer" originates from the Greek word ''meros'', which means "a part". The word polymer derives its meaning from this, which means "many mers". A repeat unit (mer) is not to be confused with the term monomer, which refers to the small molecule from which a polymer is synthesized.Callister, William D. (2007). ''Materials science and engineering : an introduction'' (7th ed.) New York : John Wiley & Sons. One of the simplest repeat units is that of the addition polymer polyvinyl chloride, - H2-CHClsub>n-, whose repeat unit is - H2-CHCl. In this case the repeat unit has the same atoms as the monomer vinyl chloride CH2=CHCl. When the polymer is formed, the C=C ...
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Ethylene Glycol
Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol) with the formula . It is mainly used for two purposes, as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, flammable, viscous liquid. Ethylene glycol has a sweet taste, but it is toxic in high concentrations. Production Industrial routes Ethylene glycol is produced from ethylene (ethene), via the intermediate ethylene oxide. Ethylene oxide reacts with water to produce ethylene glycol according to the chemical equation: This reaction can be catalyzed by either acids or bases, or can occur at neutral pH under elevated temperatures. The highest yields of ethylene glycol occur at acidic or neutral pH with a large excess of water. Under these conditions, ethylene glycol yields of 90% can be achieved. The major byproducts are the oligomers diethylene glycol, triethylene glycol, and tetraethylene glycol. The separation o ...
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Pentaethylene Glycol Monododecyl Ether
Within chemical compound surfactants, Pentaethylene glycol monododecyl ether (C12E5) is a nonionic surfactant. It is formed by the ethoxylation chemical reaction of dodecanol (lauryl alcohol) to give a material with 5 repeat units of ethylene glycol. Multilamellar vesicle formation Within the study of biological membranes and cell biology, for vesicle formation, the lamellar phase at 40wt% solution of C12E5 (Pentaethylene glycol monododecyl ether) dissolved in D2O form multilamellar vesicles under shear rate.{{cite journal , doi = 10.1021/la1046047 , pmid = 21261313 , title = Effect of Shear Rates on the MLV Formation and MLV Stability Region in the C12E5/D2O System: Rheology and Rheo-NMR and Rheo-SANS Experiments , year = 2011 , last1 = Gentile , first1 = Luigi , last2 = Rossi , first2 = Cesare Oliviero , last3 = Olsson , first3 = Ulf , last4 = Ranieri , first4 = Giuseppe Antonio , journal = Langmuir , volume = 27 , issue = 6 , pages = 2088 See also * Octaethyle ...
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Non-ionic Surfactants
An ion () is an atom or molecule with a net electrical charge. The charge of an electron is considered to be negative by convention and this charge is equal and opposite to the charge of a proton, which is considered to be positive by convention. The net charge of an ion is not zero because its total number of electrons is unequal to its total number of protons. A cation is a positively charged ion with fewer electrons than protons while an anion is a negatively charged ion with more electrons than protons. Opposite electric charges are pulled towards one another by electrostatic force, so cations and anions attract each other and readily form ionic compounds. Ions consisting of only a single atom are termed atomic or monatomic ions, while two or more atoms form molecular ions or polyatomic ions. In the case of physical ionization in a fluid (gas or liquid), "ion pairs" are created by spontaneous molecule collisions, where each generated pair consists of a free electron and ...
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