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From Self-sufficiency
- [[Category:Ketones]]33 KB (4,541 words) - 10:57, 17 June 2016
- [[Category:Aromatic ketones]]5 KB (619 words) - 16:42, 27 September 2010
- [[Category:Ketones]]19 KB (2,731 words) - 17:52, 18 September 2010
- [[Category:Ketones]]5 KB (678 words) - 14:58, 19 September 2010
- [[Category:Ketones]]69 KB (9,697 words) - 21:01, 24 September 2010
- ...iabetic. Color change on the strip indicates the relative concentration of ketones.9 KB (1,095 words) - 16:48, 27 September 2010
- The clandestine conversion of morphine to ketones of the hydromorphone class or other derivatives like [[dihydromorphine]] (P87 KB (12,376 words) - 16:51, 27 September 2010
- [[Category:Ketones]]7 KB (885 words) - 09:43, 20 September 2010
- [[Category:Aromatic ketones]]6 KB (859 words) - 09:45, 20 September 2010
- ...rier properties, generally good chemical resistance (although acetones and ketones will attack PET) and a high degree of impact resistance and tensile strengt9 KB (1,285 words) - 15:54, 15 April 2013
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4 KB (613 words) - 10:09, 20 September 2010
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8 KB (1,277 words) - 10:09, 20 September 2010
- ...y resists chemicals such as detergents, oils, fats, acids, bases, alcohol, ketones, aliphatic hydrocarbons and hot polar solutions (including water).<ref name12 KB (1,699 words) - 10:09, 20 September 2010
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4 KB (554 words) - 10:10, 20 September 2010
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5 KB (716 words) - 10:10, 20 September 2010
- ...the normal ground state, reacts with sensitizers, such as certain dyes and ketones, excited by radiation to their triplet states. Oxygen also increases the am12 KB (1,716 words) - 10:10, 20 September 2010
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1 KB (201 words) - 10:17, 20 September 2010
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11 KB (1,689 words) - 10:17, 20 September 2010
- | SolubleOther = Soluble in ketones, alcohols and other organic solvents at high temperature2 KB (218 words) - 10:18, 20 September 2010
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5 KB (609 words) - 13:10, 20 September 2010
- [[Category:Aromatic ketones]]2 KB (227 words) - 13:12, 20 September 2010
- [[Category:Ketones]]2 KB (264 words) - 13:12, 20 September 2010
- [[Category:Aromatic ketones]]4 KB (478 words) - 13:12, 20 September 2010
- [[Category:Aromatic ketones]]3 KB (408 words) - 13:13, 20 September 2010
- Substituting formaldehyde by other aldehydes or ketones results in a 2-substituted 1,3-dioxolane (yield: 70–85%, catalyst: tetrae82 KB (11,709 words) - 21:31, 20 September 2010
- ...ent. However, when the plants were in the bag, the levels of aldehydes and ketones both decreased slowly but continuously, indicating removal by the plants" <30 KB (4,388 words) - 21:31, 20 September 2010
- ...lude solvents (alcohol, [[xylene]], [[turpentine]], esters, [[acetone]], [[ketones]], and others); metalworking fluids (neat oils, water-based metalworking fl12 KB (1,701 words) - 21:31, 20 September 2010
- [[Category:Ketones]]15 KB (2,087 words) - 21:32, 20 September 2010
- ...hased to measure one chemical (e.g. formaldehyde) or a chemical type (e.g. ketones) or a broad spectrum of chemicals (e.g. solvents). They are relatively eas36 KB (4,956 words) - 21:33, 20 September 2010
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9 KB (1,089 words) - 20:14, 21 September 2010
- ...t A. | title = Alkaline condensation of fluorinated esters with esters and ketones | year = 1947 | journal = [[Journal of the American Chemical Society]] | vo [[Category:Ketones]]2 KB (256 words) - 20:15, 21 September 2010
- ...rangement of isopropenylacetate.<ref>Hardo Siegel, Manfred Eggersdorfer “Ketones” in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, 2002, Wi [[Category:Ketones]]16 KB (2,268 words) - 20:15, 21 September 2010
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3 KB (410 words) - 20:15, 21 September 2010
- [[Category:Ketones]]8 KB (1,107 words) - 22:07, 21 September 2010
- ...he chemicals in these groups are polar and readily dissolve in alcohols or ketones (acetone), but will only partially dissolve in solvents like butane or ethy16 KB (2,480 words) - 22:10, 21 September 2010
- ...hat is somewhat bitter but with a slight sweet component characteristic of ketones in general; it is not as bitter as morphine. ...]] into [[metopon]] or acetylated morphine derivatives into the respective ketones of the [[acetylmorphone]] series.38 KB (5,300 words) - 22:13, 21 September 2010
- [[Category:Ketones]]61 KB (8,865 words) - 22:13, 21 September 2010
- [[Category:Ketones]]30 KB (4,151 words) - 22:14, 21 September 2010
- [[Category:Ketones]]2 KB (209 words) - 22:15, 21 September 2010
- [[Category:Aromatic ketones]]16 KB (2,012 words) - 22:15, 21 September 2010
- [[Category:Ketones]]3 KB (387 words) - 22:16, 21 September 2010
- [[Category:Aromatic ketones]]2 KB (256 words) - 22:16, 21 September 2010
- [[Category:Aromatic ketones]]1 KB (165 words) - 22:16, 21 September 2010
- [[Category:Aromatic ketones]]3 KB (442 words) - 22:16, 21 September 2010
- [[Category:Aromatic ketones]]11 KB (1,457 words) - 22:16, 21 September 2010
- [[Category:Aromatic ketones]]5 KB (653 words) - 22:17, 21 September 2010
- [[Category:Ketones]]3 KB (405 words) - 21:00, 24 September 2010
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33 KB (4,639 words) - 21:02, 24 September 2010
- [[Category:Ketones]]794 bytes (87 words) - 21:02, 24 September 2010