In soaps

CgHeOa. White crystals m.p. 37°C, b.p. 263°C. Occurs associated with vanillin. Obtained on oxidation of various natural products such as piperine. Used extensively in soap perfumery. 

SNG Substitute natural gas. soaps Sodium and potassium salts of fatty acids, particularly stearic, palmitic and oleic acids. Animal and vegetable oils and fats, from which soaps are prepared, consist essentially of the glyceryl esters of these acids. In soap manufacture the oil or fat is heated with dilute NaOH (less frequently KOH) solution in large vats. When hydrolysis is complete the soap is salted out , or precipitated from solution by addition of NaCl. The soap is then treated, as required, with perfumes, etc. and made into tablets. 

As improvements over P-methylumbeUiferone (55—57), 4-methyl-7-amino-coumarin [26093-31-2] (12a) and 7-dimethylamino-4-methylcoumarin [87-014] (12b) (58—61) were proposed. These compounds are used for brightening wool and nylon either in soap powders or detergents, or as salts under acid dyeing conditions. They are obtained by the Pechmaim synthesis from appropriately substituted phenols and P-ketocarboxyflc acid esters or nitriles in the presence of Lewis acid catalysts (see Coumarin). 

Germicides. Ben2otrifluoride derivatives have also found wide use as antimicrobial agents in soaps, eg, the brominated and chlorinated materials, fluorosalan [4776-06-1] and cloflucarbon [369-77-7]. 

The hydroxybenzaldehydes are used primarily as chemical intermediates for a variety of products. The largest single use of sahcylaldehyde is in the manufacture of coumarin. Coumarin is an important commercial chemical used in soaps, flavors and fragrances, and electroplating (see Coumarin). Other significant uses of both sahcylaldehyde and -hydroxybenzaldehyde are as follows. 

Lavender Oil Spike. Also known as spike oil, lavender oil spike is obtained by steam distillation of the flowering tops of l vandula latijolia Vik., which grows wild and is also cultivated throughout the Mediterranean region, with most production in Spain and France. There was a time when spike oil, particularly Spanish lavender oil [8016-78-2] found extensive use in soap perfumery however, with the introduction of the less expensive lavandin oil, a hybrid of tme lavender (L. angustifolid) and L. latijolia, utilization of spike oil in perfumery has been reduced appreciably. French spike oil, a more dehcate version, still finds considerable use in functional and industrial perfumery. A comparison of the volatiles of a commercial Spanish oil and a... 

Monobutylamines are easily soluble in water and hydrocarbons and can generally be steam distilled. These properties lead to uses in soaps for water and oil emulsions, and as corrosion inhibitors in steam boiler appHcations (see Corrosion and corrosion inhibitors Emulsions). Morpholine is also extensively used as a corrosion inhibitor in steam boiler systems. In addition, it is widely used as an intermediate in the production of delayed-action mbber accelerators. 

Other appHcations of amyl alcohols include their use as flavor and fragrance chemicals. Amyl isovalerate and amyl saHcylate consumed a maximum of 450 t of amyl alcohols (150). Isoamyl saHcylate is used to a large extent in soap and cosmetic fragrances because of its cost effectiveness (167). Isoamyl... 

Isoamyl saUcylate is perhaps the most important ester of saUcyhc acid for perfumery purposes. Generally, it is manufactured by the transesterification of methyl saUcylate. It has a characteristic flowery aroma and is useful in soap fragrances. The May 1996 price was 5.30/kg (18). Other saUcylates of commercial interest as flavor and fragrance agents include isopropyl, isobutyl, phenethyl [87-22-9] and 2-ethyIhexyl saUcylates. 

These structures are commonly referred to as hexagonal Hquid crystals. As the surfactant concentration is further increased, the tubules expand in a second direction to form large, stacked lamellar sheets of surfactants, commonly referred to as lamellar Hquid crystals. These Hquid crystals are very important in soap making. 

Framing. The framed bar process is by far the oldest and the most straightforward process utilized in the production of bar soaps. The wet base soap is pumped into a heated, agitated vessel commonly referred to as a cmtcher. The minor ingredients used in soap bars such as fragrance or preservative are added to the wet soap in the cmtcher or injected in-line after reduction of product stream temperature. The hot mixture is then pumped into molds and allowed to cool. 

Soap Bars. In soap bars the primary surfactant is predominantly sodium salts of fatty acids. These products typically contain between 70 and 85% soap. Occasionally, potassium soap ( 5-30%) is included in the formulation to increase the solubiUty of the soap and, hence, the bar s lathering properties. The low Krafft temperatures for potassium soap are the basis for the lather enhancement, but also limits their content in bars. 

Amidosulfonates. Amidosulfonates or A/-acyl-A/-alkyltaurates, are derived from taurine, H2NCH2CH2S02Na, and are effective surfactants and lime soap dispersants (Table 9). Because of high raw material cost, usage is relatively small. Technically, amidosulfonates are of interest because they are stable to hydrolysis, unaffected by hard water, and compatible with soap. They have been used in soap—surfactant toilet-bar formulations. With shorter, acyl groups, they make excellent wetting agents. 

The acetate is also usehil commercially and can be made by direct esterification of Nopol. The products are usehil in soaps, detergents, poHshes, and other household products. 

Uses ndReactions. The main use for citroneUol is for use in soaps, detergents, and other household products. It is also important as an intermediate in the synthesis of other important fragrance compounds, such as citroneUyl acetate and other esters, citroneUal, hydroxycitroneUal, and menthol. 

Minor and potential new uses include flue-gas desulfurization (44,45), silver-cleaning formulations (46), thermal-energy storage (47), cyanide antidote (48), cement additive (49), aluminum-etching solutions (50), removal of nitrogen dioxide from flue gas (51), concrete-set accelerator (52), stabilizer for acrylamide polymers (53), extreme pressure additives for lubricants (54), multiple-use heating pads (55), in soap and shampoo compositions (56), and as a flame retardant in polycarbonate compositions (57). Moreover, precious metals can be recovered from difficult ores using thiosulfates (58). Use of thiosulfates avoids the environmentally hazardous cyanides. 

Stannic chloride is also used widely as a catalyst in Eriedel-Crafts acylation, alkylation and cycHzation reactions, esterifications, halogenations, and curing and other polymerization reactions. Minor uses are as a stabilizer for colors in soap (19), as a mordant in the dyeing of silks, in the manufacture of blueprint and other sensitized paper, and as an antistatic agent for synthetic fibers (see Dyes, application and evaluation Antistatic agents). 

Benzyl Chloride. Benzyl chloride is manufactured by high temperature free-radical chlorination of toluene. The yield of benzyl chloride is maximized by use of excess toluene in the feed. More than half of the benzyl chloride produced is converted by butyl benzyl phthalate by reaction with monosodium butyl phthalate. The remainder is hydrolyzed to benzyl alcohol, which is converted to ahphatic esters for use in soaps, perfume, and davors. Benzyl salicylate is used as a sunscreen in lotions and creams. By-product benzal chloride can be converted to benzaldehyde, which is also produced directiy by oxidation of toluene and as a by-product during formation of benzoic acid. By-product ben zotrichl oride is not hydrolyzed to make benzoic acid but is allowed to react with benzoic acid to yield benzoyl chloride. 

---