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Alcohol fatty

Long chain alcohols, known as fatty alcohols, are present only in very small amounts in vegetable oil but are found in greater quantities in some marine oils (Sonntag, 1979). Fatty alcohols also exist in small amounts in vegetable [Pg.151]

The wax ester content of olive oil varies widely in different grades of olive oil, being low in extra virgin or virgin olive oil, but it is much higher in solvent-extracted grades of olive oil and this has been accepted as a method of detecting adulteration of pressed olive oil with solvent-extracted olive oil (Nota et al., 1999). [Pg.152]

The Ziegler technology produces a broad Poisson-distribution of more or less even-numbered fatty alcohols which are fractionated into blends and single cuts. The Oxo-process results in more or less highly branched, even- and odd-numbered alcohols. [Pg.224]


M.p. SS C, b.p. 2I0 C. Important fatty alcohol obtained from naturally occurring glycerides. Used in the pharmaceutical and cosmetics industries and as a gel stabilizer for greases. [Pg.371]

The varying actual orientation of molecules adsorbed at an aqueous solution-CCU interface with decreasing A has been followed by resonance Raman spectroscopy using polarized light [130]. The effect of pressure has been studied for fatty alcohols at the water-hexane [131] and water-paraffin oil [132] interfaces. [Pg.85]

The higher alcohols occur in minor quantities primarily as the wax ester (ester of a fatty alcohol and a fatty acid) in many oilseed and marine sources. Free alcohols octacosanol [557-61-9] C2gH gO, and triacontanol [28351-05-5] have been isolated in very small amounts from sugarcane and its... [Pg.440]

The first commercial production of fatty alcohol ia the 1930s employed the sodium reduction process usiug a methyl ester feedstock. The process was used ia plants constmcted up to about 1950, but it was expensive, hazardous, and complex. By about 1960 most of the sodium reduction plants had been replaced by those employing the catalytic hydrogenolysis process. Catalytic hydrogenation processes were investigated as early as the 1930s by a number of workers one of these is described ia reference 26. [Pg.446]

Off-Shoot-O. The methyl esters of the Cg—C 2 fatty acids (40) are collectively sold under the name Off-Shoot-O and are closely related to 1-decanol, the fatty alcohol sold to control axillary shoots in tobacco. The material is a contact-type chemical used to pinch ornamental plants such as a2aleas, cotoneaster, juniper Juniperus sp. privet, rhamnus, and taxus (Taxus sp. sp.). As a result of treatment the shmbs become bushier. The mode of action is by plasmolysis of the young, sensitive tissues. Therefore, appHcation timing may be critical. [Pg.426]

The most widely used alkyl sulfate in shampoo preparation is lauryl sulfate. The alkyl component of this sulfate ranges from C-10 to C-18 with a predominance of the C-12 (lauryl) component. By distillation of the fatty alcohol, certain cuts can be obtained which offer the best effects in foaming, cleansing, and rinsing properties for the alkyl sulfate preparation. The range which appears to be most desirable is between C-12 and C-16. Lauryl sulfate detergents are available in various salt forms with the sodium, ammonium, and triethanolamine types being used most frequently in shampoos. [Pg.449]

AlkylPtherSulfates. These surfactants are also found in shampoo appHcations. They are prepared similarly to alkyl sulfates except that the fatty alcohol is... [Pg.449]

A.lkyl Sulfosuccinate Half Asters. These detergents are prepared by reaction of maleic anhydride and a primary fatty alcohol, followed by sulfonation with sodium bisulfite. A typical member of this group is disodium lauryl sulfosucciaate [26838-05-1]. Although not known as effective foamers, these surfactants can boost foams and act as stabilizers when used ia combination with other anionic surfactants. In combination with alkyl sulfates, they are said to reduce the irritation effects of the latter (6). [Pg.450]

Other thickeners used include derivatives of ceUulose such as methylceUulose, hydroxypropylmethylceUulose, and ceUulose gum natural gums such as tragacanth and xanthan (see Cellulose ethers Gums) the carboxyvinyl polymers and the poly(vinyl alcohol)s. The magnesium aluminum siHcates, glycol stearates, and fatty alcohols in shampoos also can affect viscosity. [Pg.450]

Many different types of foaming agents are used, but nonionic surfactants are the most common, eg, ethoxylated fatty alcohols, fatty acid alkanolamides, fatty amine oxides, nonylphenol ethoxylates, and octylphenol ethoxylates, to name a few (see Alkylphenols). Anionic surfactants can be used, but with caution, due to potential complexing with cationic polymers commonly used in mousses. [Pg.453]

An ammoniacal solution is added just before use to activate the hydrogen peroxide. Ammonia is preferred over sodium carbonate (40) or ethanolamines for maximum bleaching. The alkaline solution can be formulated iato a shampoo vehicle with oleate soaps or ethoxylated fatty alcohols. When the bleach is appHed to areas such as new hair growth, a viscous cream or paste may be preferred, formulated with fatty alcohols, alkanolamides, or other thickeners. [Pg.458]

Additives. Because of their versatility, imparted via chemical modification, the appHcations of ethyleneimine encompass the entire additive sector. The addition of PEI to PVC plastisols increases the adhesion of the coatings by selective adsorption at the substrate surface (410). PEI derivatives are also used as adhesion promoters in paper coating (411). The adducts formed from fatty alcohol epoxides and PEI are used as dispersants and emulsifiers (412). They are able to control the viscosity of dispersions, and thus faciHtate transport in pipe systems (413). Eatty acid derivatives of PEI are even able to control the viscosity of pigment dispersions (414). The high nitrogen content of PEIs has a flame-retardant effect. This property is used, in combination with phosphoms compounds, for providing wood panels (415), ceUulose (416), or polymer blends (417,418) with a flame-retardant finish. [Pg.13]

The primary products used are fatty acids with 12—18 carboa atoms and fatty alcohols, or esters of fatty acids such as the glycerides of rapeseed and lard oil (18). Eatty acid amines and amides are used ia metal working, particularly ia emulsions (18). [Pg.242]

Most linear a-olefins are produced from ethylene. Ethylene-based capacity in 1993 was 2,196,000 t, compared to only 30,000 t for fatty alcohol-based manufacture. [Pg.437]

Linear a-olefins were produced by wax cracking from about 1962 to about 1985, and were first commercially produced from ethylene in 1965. More recent developments have been the recovery of pentene and hexene from gasoline fractions (1994) and a revival of an older technology, the production of higher carbon-number olefins from fatty alcohols. [Pg.437]

In the Godrej-Lurgi process, olefins are produced by dehydration of fatty alcohols on alumina in a continuous vapor-phase process. The reaction is carried out in a specially designed isothermal multitube reactor at a temperature of approximately 300°C and a pressure of 5—10 kPa (0.05—0.10 atm). As the reaction is endothermic, temperature is maintained by circulating externally heated molten salt solution around the reactor tubes. The reaction is sensitive to temperature fluctuations and gradients, hence the need to maintain an isothermal reaction regime. [Pg.440]

The conversion of fatty alcohols is approximately 99%. The reaction product is then condensed and sent to a distillation column to remove water and high boilers. Typically, a-olefin carbon-number distribution is controlled by the alcohol composition of the reactor feed. The process is currentiy used to produce a-olefins from fatty alcohols. A typical product composition is at <5%, at 50—70%, C g at 30—50%, C2Q at <2%,... [Pg.441]

Defoamers (qv) are available in several forms, composed of many different materials. Historically, paste and soHd defoamers were used extensively. Composed of fatty acids, fatty amides, fatty alcohols, emulsifiers (and mineral oil [8012-95-1] in the high soflds paste emulsions), these defoamers required emulsification (brick) or dilution (paste) before use. Liquid defoamers have become the preferred form, insofar as concern about handling and ovemse have been overcome. [Pg.16]

Erodings of Slow-Releasing Core Tablets. The sustained-dose portion of a dmg is granulated with hydrophobic materials such as waxes, fatty acids, or fatty alcohols and compressed into a core. The initial dose is added to the core by a modified sugar coating process or by compression coating. Thus, a tablet within a tablet is created. The core erodes slowly to release the active ingredient. [Pg.231]

Linear alpha-olefins are the source of the largest volume of ahphatic amine oxides. The olefin reacts with hydrogen bromide in the presence of peroxide catalyst, to yield primary alkyl bromide, which then reacts with dimethylamine to yield the corresponding alkyl dimethyl amine. Fatty alcohols and fatty acids are also used to produce amine oxides (Fig. 1). [Pg.191]

Fig. 1. Routes to teitiaiy amines from fatty acids oi fatty alcohols. Fig. 1. Routes to teitiaiy amines from fatty acids oi fatty alcohols.
The principal iadustrial production route used to prepare fatty amines is the hydrogenation of nitriles, a route which has been used since the 1940s. Commercial preparation of fatty amines from fatty alcohols is a fairly new process, created around 1970, which utilizes petrochemical technology, Ziegler or Oxo processes, and feedstock. [Pg.220]

Synthesis and Manufacture of Amines. The chemical and busiaess segments of amines (qv) and quaternaries are so closely linked that it is difficult to consider these separately. The majority of commercially produced amines origiaate from three amine raw materials natural fats and oils, a-olefins, and fatty alcohols. Most large commercial manufacturers of quaternary ammonium compounds are fully back-iategrated to at least one of these three sources of amines. The amines are then used to produce a wide array of commercially available quaternary ammonium compounds. Some iadividual quaternary ammonium compounds can be produced by more than one synthetic route. [Pg.381]

OleFns and Fatty Alcohols. Alkylbenzyldimethylammonium (ABDM) quatematies are usually prepared from a-olefin or fatty alcohol precursors. Manufacturers that start from the fatty alcohol usually prefer to prepare the intermediate alkyldimethylamine direcdy by using dimethylamine and a catalyst rather than from fatty alkyl chloride. Small volumes of dialkyldimethyl and alkyltrimethyl quatematies in the Cg—range are also manufactured from these precursors (Fig. 4). [Pg.381]

Fig. 4. Quaternaries from a-ole ins of fatty alcohols where R is a fatty alkyl group. The product is alkylhen yl dimethyl quaternary. Fig. 4. Quaternaries from a-ole ins of fatty alcohols where R is a fatty alkyl group. The product is alkylhen yl dimethyl quaternary.
Dispersants (qv) have been added to the pulper to maintain stickies in a colloidal state. The small particle size reduces the problems stickies cause on the paper machine and in paper products. Among the chemicals that have been used are fatty alcohol ethoxylates, alkylphenol ethoxylates, lignosulfonates, and naphthalene sulfonates (18). [Pg.8]


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Alcohol continued fatty

Alcohol-induced fatty liver development

Alcoholic fatty liver

Alcohols fatty alcohol

Alcohols fatty alcohol

Alcohols fatty, separation

Alcohols fatty-ester synthesis

Alfol® Fatty alcohols

Aliphatic alcohols fatty

Alkyl polyglycosides fatty alcohols

Aqueous solutions oxyethylated fatty alcohols

Brij® Ethoxylated fatty alcohols

Carboxylates fatty alcohol

Detergent range, fatty alcohols

Detergent range, fatty alcohols process

Detergents from fatty alcohols

Dimeric fatty alcohols

EPAL Fatty Alcohols

Ether fatty alcohol ethers

Ethoxylated Fatty Alcohol Acrylates

Ethoxylated fatty alcohols

Ethylene oligomers Fatty alcohols

Ethylene oxide-fatty alcohol condensates

Extraction of fatty alcohol

Fatty Acids, Alcohols, and Esters

Fatty Alcohol Sulfate (FAS)

Fatty acid alcohols

Fatty acid alcohols synthesis

Fatty acid conjugates alcohols

Fatty acids and alcohols

Fatty acids and esters of monohydric alcohols

Fatty acids/alcohols/waxes

Fatty alcohol , emulsifier

Fatty alcohol condensates

Fatty alcohol dinitrobenzoates

Fatty alcohol ether sulfate

Fatty alcohol ether sulphate

Fatty alcohol ethoxy sulfates

Fatty alcohol ethoxylates

Fatty alcohol polyethylene glycol ether

Fatty alcohol polyglycol ethers

Fatty alcohol polyglycol ethers surfactants

Fatty alcohol polyglycolether

Fatty alcohol polyglycolether sulfosuccinate

Fatty alcohol propylene glycol

Fatty alcohol sulfates

Fatty alcohols , biomarker

Fatty alcohols Ziegler process

Fatty alcohols biosynthesis

Fatty alcohols commercial production

Fatty alcohols esterification

Fatty alcohols methyl ester process

Fatty alcohols oleochemicals

Fatty alcohols production

Fatty alcohols source indicators

Fatty alcohols surfactants from

Fatty alcohols synthesis

Fatty alcohols trimethylsilyl ethers

Fatty alcohols, long-chain, metalation

Fatty chain alcohols, surfactants derived

Fatty liver alcoholism

Fatty oleic alcohol

Free Fatty Alcohols

High pressure hydrogenation, fatty alcohols

Hydrogenation processes, fatty alcohol production

Hydrogenolysis of fatty esters to alcohols

Long chain fatty alcohol

Mechanical stability ethylene oxide-fatty alcohol

Natural Fatty Alcohols

Non-alcoholic fatty liver

Non-alcoholic fatty liver disease

Non-alcoholic fatty liver disease NAFLD)

Nonaethoxylated fatty alcohols

Oxyethylated fatty alcohols

Plasticizer range, fatty alcohols

Polyoxyethylenated fatty alcohol

Reaction of Fatty Alcohols

Solubility of fatty acids and alcohols

Solvents fatty alcohols

Solvents unsaturated fatty alcohols

Sulfonated fatty alcohols

Sulphated fatty alcohols

Surfactant fatty alcohols

Surfactant production, intermediates fatty alcohols

Synthetic alcohol fatty

Tallow Fatty Alcohol

The Production of Fatty Alcohols

Unsaturated fatty alcohols

Very long-chain fatty alcohols

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