2.3.1 Coumarins
The chemistry of coumarin may
be understood more vividly with the help of geometrical isomers of o-hydroxycinnamic
acids, one of which instantly yields the lactone coumarin (or benzopyran),
whereas the other fails to do so. Therefore, the former is the cis-isomer
called coumarinic acid, and the latter the trans-isomer known as
the coumaric acid as given below:
Coumarin
Synonyms cis-o-Coumarinic
acid lactone; Cumarin; Coumarinic anhydride; Tonka bean comphor.
Biological Sources Coumarin
is present in a large number of medicinal herbs, such as:
Acacia farnesiana (L.)
Willd (Fabaceae)-Cassie, Huisache; Apium graveolens L. (Apiceae)-Celery;
Artemisia dracunculus L. (Asteraceae)-Tarragon; Chamaemelum
nobile (L.) All. (Asteraceae)-Roman Camomile, English Camomile,
Camomile; Cinnamomum verum J.S. Presler (Lauraceae)-Ceylon
Cinnamon; Dipteryx odorata (Aubl.) Willd (Fabaceae)-Tonka
Bean, Tonga, Cumaru; Hyoseyamus niger L. (Solanaceae)-Henbane,
Henblain, Jusquaime; Myroxylon balsamum var. Pereirae (Royle)
Harms. (Fabaceae)-Balsam of Peru; Peumus boldus Molina (Monimiaceae)-Boldo;
Pimpinella anisum L. (Apiaceae)-Anise; and Trilisa
odoratissima (J.F.Gemel.) Cass (Asteraceae)-Deertongue, Deer's
Tongue.
Characteristic Features
Coumarin crystals have an orthorhombic and rectangular plates. They have a
pleasant, fragrant odour resembling to that of the vanilla beans and a burning
taste. The physical characteristics are, namely: mp 68-70°C and bp 297-299°C.
Its solubility in water is very poor, viz., 1g dissolves in m 400 ml of cold
and 50 ml of boiling water. However, it is freely soluble in ethanol,
chloroform, ether, oils and also in alkaline solutions of NaOH or KOH.
Uses It is used
extensively as a flavouring agent in pharmaceutical formulations.
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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