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CINNAMON OR TRUE CINNAMON - Intercom Exports

CINNAMON OR TRUE CINNAMON - Intercom Exports

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of Herisset et al (1972). This approach has been extended by Lawrence who distinguished<br />

cinnamonum sps., on the basis of presence or absence of eugenol, coumerin and orthemethoxy-cinnamaldehyde<br />

in a distilled bark oils. A major problem with this method is to<br />

distinguish between C.burmanii and C.loureirii where the eugenol content of the latter’s<br />

oil does not exceed 0.5%. it has been claimed that as little as 10% C.verum in<br />

C.burmanii can be detected by this method, and the presence of C. cassia can be detected<br />

in other sps., by the ortho-methoxy cinnamaldehyde spot.<br />

T.L.C. differenciation of the bark oils from the cinnamonum sps., of commerce<br />

Cinnamonum sps., Ortho-methoxy<br />

cinnamaldehyde<br />

C. verum<br />

C. cassia<br />

C. burmanii<br />

C. loureirii<br />

Absent<br />

Present<br />

Absent<br />

Absent<br />

Eugenol<br />

Present<br />

Absent<br />

Absent<br />

Trace<br />

Coumarin<br />

Trace-absent<br />

Present<br />

Present<br />

present<br />

Slazer has pointed out that the abundence of coumarin in the steam-distilled bark<br />

oil is not an accurate indication of its abundance in the spice since the compound does<br />

not readily distilled steam. A more accurate determination can only be achieved by<br />

examining the solvent extracts of the spices.<br />

Earlier Voelkar et al (1967) had demonstrated a two dimensional t.l.c. technique<br />

that produced a fingerprint for each cinnamon and cassia bark extract. It is claimed that<br />

this technique permitted distinction of within plus or minus 20% of one type in a ground<br />

spice mixture. The absolute reliability of this method has, however, become questioned.

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