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  2. Thymol - Wikipedia

    en.wikipedia.org/wiki/Thymol

    Thymol (also known as 2-isopropyl-5-methylphenol, IPMP), C 10 H 14 O, is a natural monoterpenoid phenol derivative of p-Cymene, isomeric with carvacrol.It occurs naturally in the oil of thyme, and it is extracted from Thymus vulgaris (common thyme), ajwain, [4] and various other plants as a white crystalline substance of a pleasant aromatic odor and strong antiseptic properties.

  3. Thymol blue - Wikipedia

    en.wikipedia.org/wiki/Thymol_blue

    Melting point: 221–224 °C (430–435 °F; 494–497 K) decomposes [1] Solubility in water. Insoluble ... Thymol blue has different structures at different pH.

  4. Carvacrol - Wikipedia

    en.wikipedia.org/wiki/Carvacrol

    It is extracted from Origanum oil by means of a 50% potash solution. It is a thick oil that sets at -20 °C to a mass of crystals of melting point 0 °C, and boiling point 236–237 °C. Oxidation with ferric chloride converts it into dicarvacrol, whilst phosphorus pentachloride transforms it into chlorcymol. [5]

  5. 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

  6. m-Cresol - Wikipedia

    en.wikipedia.org/wiki/M-Cresol

    the starting point in the total synthesis of thymol, [5] an important synthetic chemical for regions lacking natural sources of the flavor compound: [6] C 7 H 8 O + C 3 H 6 ⇌ C 10 H 14 O. synthesis of dicresulene and policresulen [citation needed] synthesis of toliprolol, tolamolol & cresatin [citation needed]

  7. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  8. Boiling points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Boiling_points_of_the...

    This is a list of the various reported boiling points for the elements, with recommended values to be used elsewhere on Wikipedia. For broader coverage of this topic, see Boiling point . Boiling points, Master List format

  9. Thymolphthalein - Wikipedia

    en.wikipedia.org/wiki/Thymolphthalein

    Melting point: 248 to 252 °C (478 to 486 °F; 521 to 525 K) (decomposes) ... Thymolphthalein can be synthesized from thymol and phthalic anhydride. See also ...