† mesityloln.

Forms: 1800s mesitilole, 1800s mesitylol, 1800s mesitylole.

Origin: Formed within English, by derivation. Etymons: mesityl n., -ol suffix.

Etymology: < mesityl n. + -ol suffix. With forms in -ole compare -ole suffix². N.E.D. (1906) gives the pronunciation as (mesi·tilǫl) /mɛˈsɪtɪlɒl/.

Chemistry. Obsolete.

1. = mesitylene n.

ΚΠ

1850 A. W. Hofmann in Q. Jrnl. Chem. Soc. 2 104 (title) On the composition of mesitilole.

1852 W. Gregory Handbk. Org. Chem. (ed. 3) 223 The reader will observe, that mesitylole is isomeric with cumole, mesidine with cumidine.

1855 H. Watts tr. L. Gmelin Hand-bk. Chem. IX. 17 Mesitylene or Mesitylol C⁶H⁴.

1872 Proc. Royal Soc. 21 54 Of the several purely methylic cumidines which are possible, two only are somewhat accurately known; these are the two bases which are derived, the one from so-called pseudocumol.., the other from mesitylol.

2. = mesitol n. rare.

ΚΠ

1892 E. F. Smith tr. V. von Richter Chem. Carbon Compounds (ed. 2) 687 Mesitylol, C₆H₂(CH₃)₃.OH..is crystalline, melts at 68–69°, and boils at 220°.

This entry has been updated (OED Third Edition, September 2001; most recently modified version published online December 2020).

单词	mesitylol
释义	† mesityloln. Forms: 1800s mesitilole, 1800s mesitylol, 1800s mesitylole. Origin: Formed within English, by derivation. Etymons: mesityl n., -ol suffix. Etymology: < mesityl n. + -ol suffix. With forms in -ole compare -ole suffix². N.E.D. (1906) gives the pronunciation as (mesi·tilǫl) /mɛˈsɪtɪlɒl/. Chemistry. Obsolete. 1. = mesitylene n. ΚΠ 1850 A. W. Hofmann in Q. Jrnl. Chem. Soc. 2 104 (title) On the composition of mesitilole. 1852 W. Gregory Handbk. Org. Chem. (ed. 3) 223 The reader will observe, that mesitylole is isomeric with cumole, mesidine with cumidine. 1855 H. Watts tr. L. Gmelin Hand-bk. Chem. IX. 17 Mesitylene or Mesitylol C⁶H⁴. 1872 Proc. Royal Soc. 21 54 Of the several purely methylic cumidines which are possible, two only are somewhat accurately known; these are the two bases which are derived, the one from so-called pseudocumol.., the other from mesitylol. 2. = mesitol n. rare. ΚΠ 1892 E. F. Smith tr. V. von Richter Chem. Carbon Compounds (ed. 2) 687 Mesitylol, C₆H₂(CH₃)₃.OH..is crystalline, melts at 68–69°, and boils at 220°. This entry has been updated (OED Third Edition, September 2001; most recently modified version published online December 2020). < n.1850
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