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Tatti

Products from the Chemicals Division, Procter Gamble Company, Cincinnati, Ohio, 1987 Mdol Tatty Mlcohols, Sherex Chemical Company, Dublin, Ohio, 1986 Vista Sufactants, Industrial Chemicals, andPlastics, Vista Chemical Company, Houston, Texas, 1987 TpalTinear Primary Mlcohols, Ethyl Corporation, Baton Rouge, Louisiana, 1985 Neodol, Shell Chemical Company, Houston, Texas, 1987 HenkelTat Paw Materials, Henkel K.-G.a.A., Dbsseldorf, Eed. Rep. Germany. [Pg.451]

Causticfusion subtotal 7 Tatty acid hydrogenation processes ... [Pg.453]

Tatty acid hydrogenation process 51 Methyl ester hydrogenation process ... [Pg.453]

Van Leyenberghlaan, The World s Tatty Acids Industry Their Deripatires and End Products,Ae wm International, Amsterdam, The Netherlands, 1986, p. E-68. [Pg.187]

E. S. Pattison, ed.. Tatty Mcids and Their Industrial Applications, Marcel Dekker, Inc., New York, 1968, p. 85. [Pg.318]

G. D. Clayton and E. Clayton, eds.. Tatty s Industrial Hygiene andToxicology, 3rd rev. ed., John Wiley Sons, Inc., New York, 1978. W. M. Grant, Toxicology oftheTye, Charles C Thomas, Spriagfield, hi., 1988. [Pg.373]

L and Pyoian found Ihe oil lo conta.iri a phenol having the ugL Dol, free tatty acids, aud a sesquiterpene having the follnw-... [Pg.526]

Marsilio Ficino, Platonic Theology (Michael J. B. AUen transL James Hankins, ed.). The I Tatti Renaissance Libraiy/Harvard University Press Cambridge Mass./ London, 2005, Book 1 Gh. 4, 55-59. [Pg.161]

Tatti Renaissance library/ Harvard University Press Cambridge Mass./London, 2005). [Pg.166]

Guemeri, S. A, and R. D. Tatty, 1956, A Study of Heat Transfer to Organic Liquids in Single Tube Natural Circulation Vertical Tube Boilers, AIChE Chem. Eng. Prog. Symp. Ser. 52(18) 69—77. (4) Gungor, K. E., and R. H. S. Winterton, 1986, A General Correlation for Flow Boiling in Tubes and Annuli, Int. J. Heat Mass Transfer 29(3) 351—358. (4)... [Pg.535]

Synthesis of tatty acids, cholesterol, and other steroids, metabolic detoxification of drugs, poisons, end NHa... [Pg.184]

Waxes are esters of tatty acids and long chain primary alcohols... [Pg.410]

Blood (e.g. glucose, tatty acids, amino acids, glutamine)... [Pg.207]

No overt signs of toxicity. After 13 weeks, 31 more than 90% of the 2,3,7,8-TCDD recovered was in tatty tissues 98% of the 2,3,7,8-TCDD had not been metabolized. Time for 50% depuration from whole body was 15 weeks and tor individual organs 8-19 weeks... [Pg.1046]

What tatty acids are produced on hydrolysis of 2-oleyl-1,3- niistearylglycerol What other triacylglycerol gives the same fatty acids and in the l same proportions as 2-oleyl-1,3-distearylglycerol ... [Pg.1079]

Structurally, these acids may he considered as the monohydroxy derivatives of the Tatty acids. Included among these acids are hydruxyacetic acid iglycollic acid) and /i-hydroxypropionic acid l/S-laclic acid). These acids generally arc syrupy liquids that tend to give up water readily and form crystalline anhydrides ihcy decompose when volatilized, and they are soluble in water and usually in alcohol and ether. [Pg.295]

Volatile Acid Number. The volatile acid number or the Reichert-Meissl number denotes the number of c.c. of N/10-alkali required to neutralise the volatile acids, soluble in water, obtained from 5 grams of butter fat, previously melted and filtered. It is determined exactly as described in flit- chapter headed Tatty Substances (Vol. I, p. 377). [Pg.36]

AitUi.i.il methyl salicylate ( nl ul tiir ii-iitni. ,.. l.ii Wfn.tl oil. Tatty oils... [Pg.295]


See other pages where Tatti is mentioned: [Pg.71]    [Pg.229]    [Pg.306]    [Pg.158]    [Pg.428]    [Pg.384]    [Pg.406]    [Pg.120]    [Pg.191]    [Pg.219]    [Pg.192]    [Pg.79]    [Pg.208]    [Pg.208]    [Pg.318]    [Pg.132]    [Pg.1084]    [Pg.229]    [Pg.96]    [Pg.239]    [Pg.179]    [Pg.226]    [Pg.887]    [Pg.891]    [Pg.108]    [Pg.285]    [Pg.478]    [Pg.496]    [Pg.604]   
See also in sourсe #XX -- [ Pg.627 ]




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