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  2. Diphenhydramine - Wikipedia

    en.wikipedia.org/wiki/Diphenhydramine

    Diphenhydramine, available in various salt forms, [73] such as citrate, [74] [75] hydrochloride, [76] and salicylate, [77] exhibits distinct molecular weights and pharmacokinetic properties. Specifically, diphenhydramine hydrochloride and diphenhydramine citrate possess molecular weights of 291.8 g/mol [ 78 ] and 447.5 g/mol , [ 79 ] respectively.

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9

  4. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  5. Triprolidine - Wikipedia

    en.wikipedia.org/wiki/Triprolidine

    Melting point: 60 °C (140 °F) ... Triprolidine is used less frequently and has been replaced in popular medications by other antihistamines like Diphenhydramine, ...

  6. Melting point - Wikipedia

    en.wikipedia.org/wiki/Melting_point

    For example, the melting point of silicon at ambient pressure (0.1 MPa) is 1415 °C, but at pressures in excess of 10 GPa it decreases to 1000 °C. [13] Melting points are often used to characterize organic and inorganic compounds and to ascertain their purity. The melting point of a pure substance is always higher and has a smaller range than ...

  7. 2C-H - Wikipedia

    en.wikipedia.org/wiki/2C-H

    Melting point 138 to 139 °C (280 to 282 °F; 411 to 412 K) ( hydrochloride ) Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

  8. Diphenylamine - Wikipedia

    en.wikipedia.org/wiki/Diphenylamine

    Diphenylamine is produced by the thermal deamination of aniline over oxide catalysts: . 2 C 6 H 5 NH 2 → (C 6 H 5) 2 NH + NH 3. It is a weak base, with a K b of 10 −14.With strong acids, it forms salts.

  9. Chloral hydrate - Wikipedia

    en.wikipedia.org/wiki/Chloral_hydrate

    Chloral hydrate is a geminal diol with the formula Cl 3 C−CH(OH) 2.It was first used as a sedative and hypnotic in Germany in the 1870s. Over time it was replaced by safer and more effective alternatives but it remained in usage in the United States until at least the 1970s. [4]