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Procter Gamble Methyl Esters

Chemical Properties CMS Cl-flO CH09S CHZIt CH D CH2ft CHttS CHHt CHS97 [Pg.851]

KESSCOIPM ISOPROPYL MYRISTATE Liquid IPM has a dry, velvety, non-oily feel due to Its ready absorption Into skin. Generally used in premium formulations for velvety emolliency. [Pg.852]

KESSCO IPP ISOPROPYL PALMITATE Liquid IPP Is a dry, soft non-olly emoinent generally used In economical formulations. Excellent solvent for mineral oil, silicone and lanolin. [Pg.852]

KESSCO OCTYL PALMITATE OCTYL PALMITATE Liquid Dry, light, silky emollient. Enhances gloss In hair grooming pr ucts. Can be used as a binder In pressed powder makeup. [Pg.852]

KESSCO OCTYL ISONONANOATE OCTYL ISONONANOATE Liquid Very dry, non-oily properties that allow the skin to breathe. Has the lowest freeze point (-30 C) of all alcohol esters. May be used In antiperspirants, hair sprays and creams/lotions. [Pg.852]


There are basically two types of hydrogenation processes— hydrogenation of methyl esters and hydrogenation of fatty acids —with the former predominating in the U.S. Ashland and Procter Gamble, the two U.S. fatty alcohol producers, both utilize methyl ester-based processes (3) ... [Pg.94]

Soybean oil was supplied by Procter and Gamble Inc., Toronto, Ontario, Canada. Methyl ester was made by the one-phase method employing a methanol/oil molar ratio of 27 1, tetrahydrofu as cosolvent and 1.0 wt.% sodium hydroxide based on the oil. The methyl ester accounted for 99,7% of the total ester present. The Alcan AA 200 activated alumina used was supplied by Alcan Chemicals, Brockville. Ontario, Canada. The catalyst s BET surface area is 270-290 /g, and its pore volume is 40 cmVg. The pore distribution is binodal, with 66% of pore volume in pores Jess than 30 radius and the rest in larger pores. Its bulk density is 0.75 g/cm... [Pg.1519]

Figure 13.4). This route first produces fatty acids which are then hydrogenated to produce alcohols. Another common route for converting triglycerides to alcohols involves the transesterification of triglycerides to methyl esters, which are then hydrogenated to alcohols (Figure 13.4). This process is practiced by Procter Gamble, Henkel and Kao. Figure 13.4). This route first produces fatty acids which are then hydrogenated to produce alcohols. Another common route for converting triglycerides to alcohols involves the transesterification of triglycerides to methyl esters, which are then hydrogenated to alcohols (Figure 13.4). This process is practiced by Procter Gamble, Henkel and Kao.

See other pages where Procter Gamble Methyl Esters is mentioned: [Pg.67]    [Pg.851]    [Pg.67]    [Pg.851]    [Pg.446]    [Pg.217]    [Pg.446]    [Pg.253]    [Pg.446]    [Pg.403]    [Pg.2602]    [Pg.165]    [Pg.306]    [Pg.76]   


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