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  • ...such as sulfur and iodine. It readily mixes with other polar and non-polar solvents such as water, [[chloroform]], and [[hexane]]. With higher [[alkane]]s (sta [[Category:Solvents]]
    11 KB (1,554 words) - 14:43, 18 November 2023
  • ...moderately soluble in water (73 g/L at 25 °C), but miscible with organic solvents such as [[acetone]], [[ethanol]], [[ethyl acetate]]. It boils at 117.7 °C ...agent, and its presence may affect various chemical reactions done in said solvents. [[Xylene]] also appears in some butanol-containing products.
    7 KB (908 words) - 21:07, 12 September 2019
  • ...nners, and its presence may affect various chemical reactions done in said solvents. [[Category:Solvents]]
    5 KB (531 words) - 22:48, 26 July 2018
  • ...impurities from these which is often required for store-bought or homemade solvents, can be accomplished by many means, depending on the solvent. ...nd relative to its solubility in pure water. This is mostly used for polar solvents that are miscible or highly soluble in water, especially when normal distil
    19 KB (2,493 words) - 16:52, 25 July 2023
  • | SolubleOther = Miscible with almost all organic solvents<br>Immiscible with perfluorocarbons ...0.789 g/cm<sup>3</sup> and is miscible with water, as well as most organic solvents. Ethanol forms an azeotrope with water at 95.6% and solutions with higher c
    14 KB (1,953 words) - 20:56, 9 September 2023
  • [[Category:Solvents]] [[Category:Polar solvents]]
    8 KB (996 words) - 15:05, 18 November 2023
  • ...n, 1985</ref> Methanol is miscible with a variety of organic and inorganic solvents, though not as many as [[ethanol]]. Methanol/water mixtures can be separate [[Category:Solvents]]
    11 KB (1,601 words) - 18:39, 9 July 2023
  • ...lar liquid. It is poorly soluble in water, but miscible with other organic solvents, such as alcohols. It freezes at −29 °C and boils at around 100 °C. ...NM by weight, which boils at 83.6°C. It forms also azeotropes with other solvents, most importantly methanol (8% NM at 64.5 °C) and ethanol (26.8% NM at 76
    10 KB (1,375 words) - 20:01, 16 May 2023
  • ...ratory solvent, due to its property of not being flammable like many other solvents, ability to dissolve a wide range of compounds, cheapness and availability, [[Category:Solvents]]
    8 KB (1,049 words) - 23:33, 14 July 2019
  • [[Category:Solvents]] [[Category:Polar solvents]]
    8 KB (1,041 words) - 10:33, 30 July 2023
  • ...is poorly soluble in water (8.7 mL/100 mL), but miscible with many organic solvents such as [[acetone]] or [[ethanol]]. It has a boiling point of 107.89 °C an [[Category:Solvents]]
    5 KB (552 words) - 14:42, 19 April 2020
  • Propionic acid is a colorless liquid, miscible with water and organic solvents. It has a rancid smell, reminiscent of body sweat. It can be salted out fro [[Category:Solvents]]
    8 KB (1,012 words) - 19:14, 12 September 2021
  • [[Category:Solvents]] [[Category:Polar solvents]]
    4 KB (506 words) - 18:40, 27 May 2023
  • ...nd all protic solvents. It is however miscible and soluble in most aprotic solvents, such as [[benzene]], [[carbon tetrachloride]], [[chloroform]], [[diethyl e
    7 KB (931 words) - 21:18, 22 October 2022
  • [[Category:Solvents]] [[Category:Polar solvents]]
    6 KB (674 words) - 19:08, 3 November 2023
  • ...It reacts with bases and amines, while miscible with [[water]] and organic solvents. [[Category:Solvents]]
    6 KB (682 words) - 17:27, 27 May 2023
  • [[Category:Solvents]] [[Category:Polar solvents]]
    4 KB (499 words) - 20:00, 7 September 2020
  • ...s a colorless liquid, poorly soluble in water, but more soluble in organic solvents. [[Category:Solvents]]
    4 KB (451 words) - 18:29, 21 July 2019
  • It forms azeotropes with a variety of solvents, most notably water at 95.8 °C (54.4 % water, 45.6 % n-pentanol).<ref>L. H [[Category:Solvents]]
    5 KB (605 words) - 20:50, 27 July 2022
  • ...pleasant. It is somewhat soluble in water, but miscible with other organic solvents, like alcohols and halocarbons. [[Category:Solvents]]
    5 KB (564 words) - 21:00, 12 September 2019
  • ...g stores as solvent, mostly pure, though most of the time mixed with other solvents. [[Category:Solvents]]
    5 KB (621 words) - 10:50, 9 September 2023
  • ...id, with a fruity odor, slightly soluble in water, but miscible in organic solvents. ...diethyl ether, [[dimethyl sulfoxide]] or [[dimethylformamide]] are used as solvents instead.<ref>Shao, Yi-Ming; Yang, Wen-Bin; Kuo, Tun-Hsun; Tsai, Keng-Chang;
    7 KB (850 words) - 22:48, 20 January 2020
  • ...]], or [[methyl cellosolve]] (ethylene glycol monomethyl ether). Alcoholic solvents like these give 1 : 1 reaction stoichiometry. === Additives / co-solvents ===
    10 KB (1,556 words) - 18:24, 17 April 2019
  • ...t reacts with all protic solvents, but is very soluble in many hydrocarbon solvents, like alkanes and aromatics.
    7 KB (843 words) - 22:43, 17 November 2020
  • ...iquid, with a pungent aromatic odor. It reacts with water and other protic solvents.
    6 KB (662 words) - 10:16, 7 July 2022
  • Solvents can be broadly classified into two categories: polar and non-polar. A speci ...ty of water is indicated by its high dielectric constant of 88 (at 0 °C). Solvents with a dielectric constant of less than 15 are generally considered to be n
    2 KB (288 words) - 19:42, 11 October 2022
  • ...c and a powerful lachrymator. It reacts with water and alcohols and protic solvents, but dissolves in halocarbons.
    8 KB (1,050 words) - 20:53, 5 November 2023
  • ...th the application of alkali cyanides such as [[sodium cyanide]] and polar solvents the reaction type is an S<sub>N</sub>2 reaction whereby the alkyl halide is ...ciples, the carbon center is more basic and more nucleophilic. When protic solvents are used, the resulting greater solvation of this carbon center is thought
    3 KB (522 words) - 18:44, 11 March 2024