Fragrance additives

Fragrance additives, designed to impart or mask an odom... 

One of the most prominent MT-hydrocarbons is (+)-limonene, which occurs in nearly every EO of the citrus oils and is a major compound (up to 97 % [11]) in sweet orange oil (from the peel of Citrus sinensis (L.) Osbeck, syn. Citrus aurantium var. sinensis). Its odor is reminiscent of the typical sweet orange flavor, whereas its antipode (-)-limonene possesses an odor that recalls turpentine [12]. Sweet orange oil achieves its main importance in the flavor and food industry because it is easily obtainable (yield 5 % [11]) and due to its pleasant odor, which is accepted by everyone and is caused by the character impact compound [13] (+)-limonene. In the past, the use of (+)-limonene has experienced a great expansion. Besides its use in the food industry, it is used as flavor and fragrance additive in cosmetics, soaps, and perfumes, and also in medicine to mask the bitter taste of... 

Cosmetics Personal application products fragrance additives Perfume and cologne development product enhancement consumer appeal... 

Uses Emollient, solubilizer, coupling agent in creams, lotions, bath oils, men s grooming aids, topical pharmaceuticals plasticizer fragrance additive solvent props. penetrant for topical pharmaceuticals emollient, emulsifier, thickener, stabilizer, opacifier, pearlescent for creams, shaving creams, cream shampoos Features Liquid feel Regulatory Canada DSL... 

In certain brilliantine compositions, vegetable and animal oils are used as substitutes for mineral oil. In these systems, because of their potential for rancidity, antioxidants must be included. Other alternatives to mineral oils that have found utiHty in brilliantines are the polyethylene glycols which come in a variety of solubiHties and spreading properties. Use of these materials offers the advantage of chemical stabiHty to rancidity. Other additives found in brilliantines to improve their aesthetics include colorants, fragrance, medicated additives, lanolin, and fatty acid esters. 

Solvents. The most widely used solvent is deionized water primarily because it is cheap and readily available. Other solvents include ethanol, propjdene glycol or butylene glycol, sorbitol, and ethoxylated nonionic surfactants. There is a trend in styling products toward alcohol-free formulas. This may have consumer appeal, but limits the formulator to using water-soluble polymers, and requires additional solvents to solubilize the fragrance and higher levels of preservatives. 

Gc/ftir has both industrial and environmental appHcations. The flavor and aroma components in fragrances, flavorings, and foodstuffs can be identified and quantified via gc/ftir (see Food additives). Volatile contaminants in air, water, and soil can be analy2ed. Those in air are usually trapped in a sorption tube then injected into the chromatograph. Those in water or soil are sparged, extracted, or thermally desorbed, then trapped and injected (63,64). 

Acetophenone can react with formaldehyde to yield light-resistant resins which are used as additives in nitrocellulose paints. It is also used as a photoinitiator, and in the pharmaceuticals, perfumery, and pesticide industries (344). It can be hydrogenated to 1-phenylethanol which is used for the production of aromatic ester fragrances (345). Technical-grade acetophenone is available at 2.29/kg perfume-grade acetophenone was 6.50/kg in October 1994. 

Knoevenagel condensation of malonic acid with heptaldehyde [111-71-7] followed by ring closure, gives the fragrance y-nonanoic lactone [104-61-0] (6) (14). Beside organic synthesis, malonic acid can also be used as electrolyte additive for anodization of aluminum [7429-90-5] (15), or as additive in adhesive compositions (16). 

A commercially important outlet in the fragrance industry is the methyl dihydrojasmonate [24851-98-7] (26) which is made by Michael addition of a malonate to 2-pentyl-2-cyclopenten-l-one [91791 -21 -8] (52) and which is used in perfumery for blossom fragrances, particularly jasmine (see Perfumes). 

Liquid Fabric Softeners. The principal functions of fabric softeners are to minimize the problem of static electricity and to keep fabrics soft (see Antistatic agents). In these laundry additives, the fragrance must reinforce the sense of softness that is the desired result of their use. Most fabric softeners have a pH of about 3.5, which limits the materials that can be used in the fragrances. For example, acetals cannot be used because they break down and cause malodor problems in addition, there is the likelihood of discoloration from Schiff bases, oakmoss extracts, and some specialty chemicals. Testing of fragrance materials in product bases should take place under accelerated aging conditions (eg, 40°C in plastic bottles) to check for odor stabiUty and discoloration. 

The odd-carbon stmcture and the extent of branching provide amyl alcohols with unique physical and solubiUty properties and often offer ideal properties for solvent, surfactant, extraction, gasoline additive, and fragrance appHcations. Amyl alcohols have been produced by various commercial processes ia past years. Today the most important iadustrial process is low pressure rhodium-cataly2ed hydroformylation (oxo process) of butenes. 

Isopropyl alcohol is also employed widely as a solvent for cosmetics (qv), eg, lotions, perfumes, shampoos, skin cleansers, nail poHshes, makeup removers, deodorants, body oils, and skin lotions. In cosmetic appHcations, the acetone-like odor of isopropyl alcohol is masked by the addition of fragrance (144). 

H)- and (+)-1imonenes are widely used ia the manufacture of terpene resias. Additionally, a (-)-limonene and (+)- P-pheUandrene mixture from sulfate turpentine has been used to produce terpene resias. (+)-Limoaeae from the citms iadustry coatiauaHy fiads aew uses as a solveat aot only for its solvency properties but also for its orange oil fragrance. 

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