Cosmetic preparations

Keta.Is, Trimethylpentanediol reportedly forms a cycHc ketal by heating it with benzophenone ia the presence of sulfonic acid catalysts at reflux temperatures ia toluene (64). These are said to be useful as aprotic solvents for ink-jet printing and as inflammation inhibitors for cosmetic preparations... 

Abbreviations of prominent use properties of the various classes of commercial surfactants are shown in Table 1. Antimicrobial activity includes germicidal, bactericidal, and bacteriostatic effects emolliency describes lubrication or a soft feel imparted to skin by surfactants a hair conditioner is a substantive surfactant appHed from aqueous solution to impart a lubricating or antistatic effect and opacifters are used to thicken hand-dishwashing products and cosmetic preparations to convey an appearance of high concentration and to retard solvent drainage from foam. 

Eatty acid ethoxylates are used extensively in the textile industry as emulsifiers for processing oils, antistatic agents (qv), softeners, and fiber lubricants, and as detergents in scouring operations. They also find appHcation as emulsifiers in cosmetic preparations and pesticide formulations. Eatty acid ethoxylates are manufactured either by alkaH-catalyzed reaction of fatty acids with ethylene oxide or by acid-catalyzed esterification of fatty acids with preformed poly(ethylene glycol). Deodorization steps are commonly incorporated into the manufacturing process. 

Lanolin alcohols are obtained by saponification of purified wool grease, a mixture of high molecular esters that is recovered in wool (qv) scouring. Ethoxylation of purified lanolin alcohols yields a full series of lipophilic and hydrophilic nonionic emulsifiers whose largest use is in cosmetic preparations. Manufacturers include Amerchol, Croda, ICI, Henkel Corporation, Westbrook Lanolin, Witco, and Pulcra, SA. 

OC-Bisabolol. a-Bisabolol (99) occurs in camomile flowers and has been shown to be the main antiphlogistic and spasmolytic component of the European medicinal plant. The use of bisabolol is recommended mainly for its pharmacodynamic properties in cosmetic preparations for skin protection. 

Nonfood preservative appHcations of sodium and potassium benzoate are found in pharmaceutical and cosmetic preparations, such as toothpastes and powders, tobacco, pastes and glue, as well as starch and latex (36,37). 

As of 1991 in the United States, OTC antiacne preparations may contain only a few active dmgs, for example, sulfur [7704-34-9] resorcinol acetate [102-29-4], resorcinol [108-46-3], salicylic acid [69-72-7], and some combinations (52). OTC anti-acne constituents maybe included in a variety of conventional cosmetic preparations, which then become OTC dmgs. These include lotions, creams, solutions, facial makeups, facial cleansers (including abrasive cleansers), and astringents. Products must contain the specified dmgs at the designated concentrations. Compositions of antiacne products have beenpubhshed (53). 

A. Nowak, Cosmetic Preparations, Micelle Press, London, 1991. 

Carbopol is widely used in cosmetic and pharmaceutical practice as a gel-former. Carbopol resins are hydrophilic polymers which swell in water solutions and transform into the gel form at neutralization. At the elaboration of special cosmetic preparations in which carbopol is used, the problem of raw materials compatibility appears. For example, some extracts of aromatic pectin containing materials destroy the gel structure of carbopol. High contents of bivalent metal ions, in particular calcium ions, destructively influence onto the gel-making ability of the system too. 

The analysis and summarizing of data obtained allowed to establish the norms of Stevia and Sudanese Rose extracts content in compositions of cosmetic preparations in the gel fonu. 

Aerosol cans which may contain a propellant together with products such as paints, cleaners, cosmetic preparations and foodstuffs. These may also contain some oxygen. 

Sodium lauryl sulfate is often used in medicinal preparations. As mentioned above, it is used as an emulsifer for creams and lotions in cosmetic preparations, but due to its low toxicity and biological compatibility it is also used in the preparation of creams, gels, and emulsions in which the medications are dispersed. Its ability to lower the interfacial tension affects the potentiation and availability of medications. 

Parker M.T. (1972) The clinical significance ofthe presence of microorganisms in pharmaceutical and cosmetic preparations. JSoc Cosm Chem, 23, 415-426. 

Safflower, also known as bastard saffron, is a yellow dye that has been used for well over three millennia, having been identified in fabrics from the Egyptian twelfth dynasty. It is derived from the safflower plant, carthamus tinctoria, native to southern Asia and the Middle East. The coloring matter in the plants is a mixture of two components one is yellow, known as safflower yellow B the other, carthamin, is red. Safflower yellow B dissolves in water when fresh safflower flowers are washed with acidulated water. Evaporating the water from the filtered solution leaves the dye as a residue in the form of a powder. Following removal of the yellow component, the red constituent of safflower, carthamin, can be extracted from the flowers by washing them with hot water. In the East, carthamin was widely used in the past, mainly for making cosmetic preparations. 

Cotte, M., P. Dumas, G. Richard, R. Breniaux, and Ph. Walter (2005), New insight on ancient cosmetic preparation by synchrotron-based infrared microscopy, Anal. Chim. Acta 553, 105-110. 

Moore MR, Meredith PA, Watson WS, et al. 1980. The percutaneous absorption of lead-203 in humans from cosmetic preparations containing lead acetate, as assessed by whole-body counting and other techniques. Food Cosmet Toxicol 18 399-405. 

In addition, in the USA ether sulfates are used on a large scale in laundry detergents. For that reason, their market share in the USA is even larger than in Europe (3), At present, alkyl ether sulfates are primarily useH in the form of their Na salts. In the past, however, cosmetic preparations containing ammonium and Mg salts have also been quite common (4). 

Uses Preparation of sodium and butyl benzoates, benzoyl chloride, phenol, caprolactum, and esters for perfume and flavor industry plasticizers manufacture of alkyl resins preservative for food, fats, and fatty oils seasoning tobacco dentifrices standard in analytical chemistry antifungal agent synthetic resins and coatings pharmaceutical and cosmetic preparations plasticizer manufacturing (to modify resins such as polyvinyl chloride, polyvinyl acetate, phenol-formaldehyde). 

The human skin is a rather complex structure, which protects the body against the environment. The aim of the different cosmetics is to repair and restore the original balance of elements in skin structure. Cosmetic preparations would need to consider any reaction between them and the components of the skin. Skin creams are known to be composed of a variety of ingredients, which are based on end use (hands, feet, face, hair, etc.), and some speciality products that are applied to the skin to repair effects such as dryness. We will now consider some recipes for skin creams. Since the number of personal care emulsion creams is very large, only a few typical examples are given here. A variety of emulsion skin care products are found commercially that claim to exhibit properties for nurturing and protecting the skin. 

Ahsan, E., ]. ]. Arnold, E. Meezan, and D. ]. Pillion. Sucrose cocoate, a component of cosmetic preparations, enhances nasal and ocular peptide absorption. Int J Pharm 2003 251(1-2) 195-203. 

The trichloromethylthiocarboximides have been used for many years as agricultural fungicides they have more recently found industrial applications and are among the most stable biocides available. Both the dicarboximide (19) and the phthalimide (20) provide protection for plastics a purified form of (19) is also available and recommended as a fungicide for cosmetic preparations. 

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