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Glycerol acetate

Glycerol Acetic anhydride, hypochlorites, chromium(VI) oxide, perchlorates, alkali peroxides, sodium hydride... [Pg.1208]

Menthone glycerol acetal, 24 525 (—)-Menthoxy acid chloride, chiral derivatizing reagent, 6 76t Menthyl anthranilate, cosmetic uv absorber, 7 846t... [Pg.562]

The simultaneous measurement of multiple components in a high-density recombinant E. coli production process was reported by Macaloney et al.36 This well-written paper completely describes the methodology by which glycerol, acetate, ammonium, and dry weight were predicted. The manner in which these equations may be used as real-time control and analysis mechanisms is demonstrated. For comparison, the SEP values for glycerol, acetate, ammonium, and dry weight were, respectively, 0.6 g/1, 1.9 g/1, 13 mM, and 1.3 g/1. From a simplicity perspective, the equations were basic MLR in nature. [Pg.392]

The final proof of the gluconeogenic function of FDPase came from observations with mutants lacking this enzyme. Bacterial strains deficient in a specific FDPase (17) were found to be incapable of growth on compounds such as glycerol, acetate, or succinate. Similar metabolic defects have recently been described in man (18, 19). Children with... [Pg.614]

Toda, F., Matsuda, S., and Tanaka, K. (1991) Efficient Resolution of Secondary Alcohols, Cyanohydrins, and Glycerol Acetates by Complexation with the Host Derived from Tartaric Acid, Tetrahedron Asymm., 2, 983-986. [Pg.45]

Glycerol acetate dinitrate has been proposed as an additive to nitroglycerine in order to depress the solidification point of the latter. It has so far not been employed in practice. [Pg.206]

Among esters of gjycerol with nitric and organic acids the most important appears to be Glycerol Acetate Diniirate (X) described by Meyer [72 73]... [Pg.163]

The reagent has been used as catalyst for the preparation of 1,2-cyclic glycerol acetals by transacetalation. Thus a mixture of 30 g. of hexadecanal dimethyl acetal. [Pg.562]

Lapetina, E. G. Rodriguez de Laes Arnaiz, G. and De Robertis, E. (1969) Turnover rates for glycerol, acetate, and orthophosphate in phospholipids of the rat cerebral cortex. Biochim. biophys. Acta (Amst.), 176,643-646. [Pg.52]

Colorless Or slightly yellow, transparent brittle practically odorless, tasteless sheets, flakes, or coarse powder Swells up and absorbs 5 -10 times its weight of water to form a gel in solutions below 35 40. Sol in hot water glycerol, acetic acid. Insol in organic solvents. Amphoteric. [Pg.685]


See other pages where Glycerol acetate is mentioned: [Pg.644]    [Pg.168]    [Pg.201]    [Pg.20]    [Pg.240]    [Pg.165]    [Pg.869]    [Pg.14]    [Pg.604]    [Pg.294]    [Pg.219]    [Pg.119]    [Pg.27]    [Pg.206]    [Pg.126]    [Pg.744]    [Pg.645]    [Pg.336]    [Pg.3230]    [Pg.413]    [Pg.210]    [Pg.330]    [Pg.209]    [Pg.148]    [Pg.199]    [Pg.198]    [Pg.484]    [Pg.599]    [Pg.421]    [Pg.105]    [Pg.330]   
See also in sourсe #XX -- [ Pg.31 , Pg.33 ]




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Acetal glycerol

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