quinamicinen.

Brit.

/kwᵻˈnamᵻsiːn/, U.S.

/kwəˈnæmˌsin/

Origin: A variant or alteration of another lexical item; modelled on a German lexical item. Etymon: quinamine n.

Etymology: < quinamine n., with insertion of -ic- (perhaps compare conicine n., solanicine n., etc.), after German Chinamicin (O. Hesse 1881, in Ann. der Chem. 207 294). Compare quinamidine n.

Chemistry. Now rare.

A substance produced by reaction of quinamine with an acid, originally thought to be an isomer of quinamine (see quots. 1939 and 1969).

ΚΠ

1881 Jrnl. Chem. Soc. 40 925 Quinamicine, C₁₉H₂₄N₂O₂.—This body is formed in small quantities, together with quinamidine, when quinamine is heated with acids.

1939 Thorpe's Dict. Appl. Chem. (ed. 4) III. 168/2 Together with quinamidine is always formed in smaller amount another isomeride, quinamicine.

1969 Phytochem. 8 650 Kirby obtained a crude material, ‘quinamicine’, on refluxing quinamine with dilute acetic acid; however this product was later found to be impure quinamidine.

This entry has been updated (OED Third Edition, December 2007; most recently modified version published online March 2022).

单词	quinamicine
释义	quinamicinen. Brit. /kwᵻˈnamᵻsiːn/, U.S. /kwəˈnæmˌsin/ Origin: A variant or alteration of another lexical item; modelled on a German lexical item. Etymon: quinamine n. Etymology: < quinamine n., with insertion of -ic- (perhaps compare conicine n., solanicine n., etc.), after German Chinamicin (O. Hesse 1881, in Ann. der Chem. 207 294). Compare quinamidine n. Chemistry. Now rare. A substance produced by reaction of quinamine with an acid, originally thought to be an isomer of quinamine (see quots. 1939 and 1969). ΚΠ 1881 Jrnl. Chem. Soc. 40 925 Quinamicine, C₁₉H₂₄N₂O₂.—This body is formed in small quantities, together with quinamidine, when quinamine is heated with acids. 1939 Thorpe's Dict. Appl. Chem. (ed. 4) III. 168/2 Together with quinamidine is always formed in smaller amount another isomeride, quinamicine. 1969 Phytochem. 8 650 Kirby obtained a crude material, ‘quinamicine’, on refluxing quinamine with dilute acetic acid; however this product was later found to be impure quinamidine. This entry has been updated (OED Third Edition, December 2007; most recently modified version published online March 2022). < n.1881
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