Synthetic sulfation, alcohols

Synthetic ethyl alcohol (known as ethanol to differentiate it from fermentation alcohol) was originally produced hy the indirect hydration of ethylene in the presence of concentrated sulfuric acid. The formed mono-and diethyl sulfates are hydrolyzed with water to ethanol and sulfuric acid, which is regenerated ... 

Sodium C12-18 alkyl sulfate Synonyms Sodium Cl2-18 alcohols sulfate Definition Sodium salt of the sulfate of a mixture of synthetic fatty alcohols with 12-18 carbons in alkyl chain... 

AESs are anionic surfactants made by sulfating alcohol ethoxylates, and the degree of ethoxyl-ation typically ranges from 1 to 4, but predominantly 2-3 moles of ethoxylation (EO) are used with both natural and synthetic alcohol sources. AES provides numerous benefits such as high solubility. 

Natural C12-C16 fatty alcohols or C10-C15 synthetic fatty alcohols with 1-4 moles of EO. These nonionics are typically used as feedstocks for sulfonation to produce a wide range of ether sulfates used in household, personal care, and industrial applications (see Section 1.6.2.1). 

Natural C12-C16 fatty alcohols or C10-C15 synthetic fatty alcohols with >4 moles ofEO. Alcohol ethoxylates with 5-11 moles of EO are used in liquid and powdered laundry detergents as coactives with LAS and fatty alcohol ethers sulfate (FAES) in hard surface-cleaning formulations and in a host of industrial applications. Alcohol ethoxylates with 12-50 moles of EO and their respective sulfated and phosphated derivatives find use in emulsion polymerization and other select applications. 

Higher n-olefins of Cs-Ci4 are used as intermediates in the manufacture of several types of surfactant materials. Linear internal olefins are used in the production of linear alkylbenzene alkylphenol detergent alcohols, which in turn is used to produce alcohol sulfates, alcohol ethoxylates, and alcohol ether sulfates and synthetic lubricants. a-Olefins are used in the production of detergent alcohols, linear alkylbenzene, synthetic lubricants, and a-olefin sulfonates (another ionic surfactant). 

Alkyl sulfates or primary alcohol sulfates (PAS), which were the first synthetic surfactants used in personal care in the United States, are mainly used in toothpaste formulations. As for the AES, the alkyl moiety is typically a mixture of Ci2-Cjg chains. According to the application, one can find sodium, ammonium, magnesium, or triethanolamine salts of fatty alcohol sulfuric acid. They are obtained by the sulfation of a fatty (natural or synthetic) primary alcohol with a mixture of air/SOj according to the following reaction ... 

Sulfation andSulfamation. Sulfamic acid can be regarded as an ammonia—SO. complex and has been used thus commercially, always in anhydrous systems. Sulfation of mono-, ie, primary and secondary, alcohols polyhydric alcohols unsaturated alcohols phenols and phenolethylene oxide condensation products has been performed with sulfamic acid (see Sulfonation and sulfation). The best-known appHcation of sulfamic acid for sulfamation is the preparation of sodium cyclohexylsulfamate [139-05-9] which is a synthetic sweetener (see Sweeteners). 

Synthetic piae oil is produced by the acid-cataly2ed hydration of mainly a-piaene derived from sulfate turpentine, followed by distillation of the cmde mixture of hydrocarbons and alcohols. The predominant alcohol obtained is a-terpiueol, although under the usual conditions of the reaction, reversible and dehydration reactions lead to multiple hydrocarbon and alcohol components (Fig. 1). 

Poly(vinyl acetate) emulsions can be made with a surfactant alone or with a protective coUoid alone, but the usual practice is to use a combination of the two. Normally, up to 3 wt % stabilizers may be included in the recipe, but when water sensitivity or tack of the wet film is desired, as in some adhesives, more may be included. The most commonly used surfactants are the anionic sulfates and sulfonates, but cationic emulsifiers and nonionics are also suitable. Indeed, some emulsion compounding formulas require the use of cationic or nonionic surfactants for stable formulations. The most commonly used protective coUoids are poly(vinyl alcohol) and hydroxyethyl cellulose, but there are many others, natural and synthetic, which are usable if not preferable for a given appHcation. 

In 1932 the first household detergent based on synthetic surfactants was brought into the market under the name FEWA (Feinwaschmittel). The product was produced from fatty alcohol sulfate by Bohme Fettchemie in Chemnitz. The shortage of the necessary natural raw materials caused by World War II led to the development of products based on more readily available raw materials [2],... 

Synthetic fibers washing (Alkylphenol ethoxylates,) fatty alcohol ethoxylates, alkane (olefine)-sulfonates, fatty alcohol (ether) sulfates, end-group-blocked fatty alcohol ethoxylates... 

Sodium alcohol sulfates are also used in the formulation of synthetic soaps and paste hand cleaners, commonly together with other surfactants and as tablet disintegrators in the case of sodium dodecyl sulfate. Sodium, but preferably ammonium and alkanolamine salts, is also used in liquid soaps. 

One of the longest known synthetically prepared surfactants are the fatty alcohol sulfates, which were prepared on technical scale before 1940. Along with their ethoxylated counterparts, the fatty alcohol ether sulfates, which appeared on the stage shortly after, their use in toiletries is very popular but they can also be found in products for textile industry and auxiliaries in emulsion polymerization. With the exception of soaps, the mentioned anionic surfactants all have a sulfur-containing functional group. Denying the differences between these, their skin irritancy potential is remarkably high. 

Although the Sharpless asymmetric epoxidation is an elegant method to introduce a specific defined chirality in epoxy alcohols and thus, in functionalized aziridines (see Sect. 2.1), it is restricted to the use of allylic alcohols as the starting materials. To overcome this limitation, cyclic sulfites and sulfates derived from enantiopure vfc-diols can be used as synthetic equivalents of epoxides (Scheme 5) [12,13]. 

While the above examples demonstrate that product control to a significant extent is possible in oxythallation by careful choice of substrate or reaction conditions, the synthetic utility of oxythallation has been illustrated most convincingly by the results obtained with highly ionic thallium(III) salts, especially the nitrate (hereafter abbreviated TTN). Unlike the sulfate, perchlorate, or fluoroborate salts (165), TTN can easily be obtained as the stable, crystalline trihydrate which is soluble in alcohols, carboxylic acids, ethers such as dimethoxyethane (glyme), and dilute mineral acids. Oxidations by TTN can therefore be carried out under a wide variety of experimental conditions. 

Methylamine occurs in herring brine 2 in crude methyl alcohol from wood distillation,3 and in the products obtained by the dry distillation of beet molasses residues.4 It has been prepared synthetically by the action of alkali on methyl cyanate or iso-cyanurate 5 by the action of ammonia on methyl iodide,6 methyl chloride,7 methyl nitrate,8 or dimethyl sulfate 9 by the action of methyl alcohol on ammonium chloride,10 on the addition compound between zinc chloride and ammonia,11 or on phos-pham 12 by the action of bromine and alkali on acetamide 13 by the action of sodamide on methyl iodide 14 by the reduction of chloropicrin,15 of hydrocyanic or of ferrocyanic acid,16 of hexamethylenetetramine,17 of nitromethane,18 or of methyl nitrite 19 by the action of formaldehyde on ammonium chloride.20... 

Monolayers are best formed from water-insoluble molecules. This is expressed well by the title of Gaines s classic book Insoluble Monolayers at Liquid-Gas Interfaces [104]. Carboxylic acids (7-13 in Table 1, for example), sulfates, quaternary ammonium salts, alcohols, amides, and nitriles with carbon chains of 12 or longer meet this requirement well. Similarly, well-behaved monolayers have been formed from naturally occurring phospholipids (14-17 in Table 1, for example), as well as from their synthetic analogs (18,19 in Table 1, for example). More recently, polymerizable surfactants (1-4, 20, 21 in Table 1, for example) [55, 68, 72, 121], preformed polymers [68, 70, 72,122-127], liquid crystalline polymers [128], buckyballs [129, 130], gramicidin [131], and even silica beads [132] have been demonstrated to undergo monolayer formation on aqueous solutions. 

Latex, Liquid Synthetic Laughing Gas Lauroyl Peroxide Lauryl Alcohol Lauryl Ammonium Sulfate Lauryl Benzene Lauryl Magnesium Sulfate Lauryl Mercaptan... 

The shift to oleochemicals has been supported by increasing environmental concerns and a preference by some consumers, especially in Europe, for materials based on natural or renewable resources. Although linear alkylbenzenesulfonates (LASs) are petrochemically based, alcohol ethoxylates, alcohol ethoxysulfates, and primary alcohol sulfates are derived from long-chain alcohols that can be either petrochemically or oleochemically sourced. There has been debate over the relative advantages of natural (oleochemical) vs synthetic (petrochemical) based surfactants. However, detailed analyses have shown there is litde objective benefit for one over the other. 

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