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Exxon Ketones

Boiiing Point at 760 mm Hg, C 79.6 Heat of Fusion, calfg mole 1.78 [Pg.651]

Evaporation Rate (BuAc = 1) 5.7 Specific Heat of Liquid, al 20°C, cal/g. 525 [Pg.651]


The physical properties of finish removers vary considerably due to the diverse uses and requirements of the removers. Finish removers can be grouped by the principal ingredient of the formula, method of appHcation, method of removal, chemical base, viscosity, or hazardous classification. Except for method of apphcation, a paint remover formulation usually has one aspect of each group, by which it can be used for one or more appHcations. A Hst of the most common organic solvents used in finish removers has been compiled (3). Many are mentioned throughout this article others include ethyl lactate [97-64-3] propylene carbonate [108-32-7] furfural alcohol [98-01-1/, dimethyl formamide [68-12-2] tetrahydrofuran [109-99-9] methyl amyl ketone [110-43-0] dipropylene glycol methyl ether [34590-94-8] and Exxate 600, a trade name of Exxon Chemicals. [Pg.550]

Materials. Phthalic anhydride (PA), adipic acid (AA), neopentyl glycol (NPG), p-hydroxybenzoic acid (PHBA), salycilic acid, m-hydroxybenzoic acid (MHBA), xylene, and methyl isobutyl ketone (MIBK) were purchased from Aldrich. p-Toluenesulfonic acid (p-TSA) was purchased from Matheson. "Aromatic 150" solvent and "Resimene 7A6", a hexakis(methyloxymethyl)melamine (HMMM) resin were supplied by Exxon and Monsanto, respectively. "Bonderite 1000" pretreated cold-rolled steel panels 3"x9"x2AGA were purchased from Parker. [Pg.336]

Hazleton Labs. 1965b. Human sensory irritation thresholds. Five ketones - final report. Prepared by Hazleton Laboratories, Inc. Falls Church, VA for Exxon Chem Amers. Houston, TX. OTS 8d submission Doc ID. 878210936, Microfiche No. 206267. [Pg.102]

Butene to methyl ethyl ketone p Exxon Beck et al. (1985)... [Pg.709]

Exxon Chlorobutyl 1065 Exxon Chlorobutyl 1066, Exxon Chlorobutyl 1068. See Isobutylene/isoprene copolymer, chlorinated ExxonMobil IPA. See Isopropyl alcohol ExxonMobil MEK. See Methyl ethyl ketone Exxpar451. See Paraffins, normal C5-20 Exx-Print 176 D Exx-Print 283 D. See Petroleum distillates, hydrotreated light Exx-PrInt 287 D. See Paraffins, normal C5-20 Exx-PrInt 588 D. See Petroleum distillates, hydrotreated middle... [Pg.1793]

Other recent patents include copolymers of tdnyl ketones with acrylates, methacrylates, and styrene (O Brien, 1993) an ethylene/carbon monoxide (1-7 wt%) blend as a photo initiator in polycaprolactone/polyethylene blends (Hirsoe, 1992) ethylene/ carbon monoxide for degradable golf tees (Akimoto) a vinyl ketone analog of Exxon s carbon monoxide/dioxapane/ethylene (Priddy, 1992) a photodegradable food wrapper based on blends of a polyolefin/starch and photo activators for the... [Pg.487]

The industrially available ketones offer a wide range of evaporation rates for the various coating applications. A solvent with excellent solvency and a fast, intermediate or slow evaporation rate for a particular coating application is available in the commercially produced ketones. Major producers of the ketones include Eastman Chemical Company, Exxon Chemical Company, Hoechst Celanese Company, Shell Chemical Company, and Union Carbide Corporation. BASF Corporation produces the cyclic ketone cyclohexanone. Acetone the lowest boiling-point ketone is produced by The Dow Chemical Company, Exxon Chemical Company, and Texaco Chemical Company. [Pg.114]


See other pages where Exxon Ketones is mentioned: [Pg.650]    [Pg.650]    [Pg.477]    [Pg.229]    [Pg.477]    [Pg.171]    [Pg.405]    [Pg.240]    [Pg.163]    [Pg.252]    [Pg.302]   


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