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The genus Cinnamomum

The genus Cinnamomum

The genus Cinnamomum

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224 K. Nirmal Babu, P.N. Ravindran and M. Shylaja<br />

Ho-oil ‘A’ (extra Ho oil):<br />

This is the best quality Ho-oil.<br />

Specific gravity at 25°C – 0.860–0.865<br />

Optical rotation – Above –14°0<br />

Refractive index (25°C) – About 1.4613<br />

Camphor content – Below 0.7%<br />

Linalool content<br />

Ho oil ‘B’ (Ho oil):<br />

– 94% or more<br />

Specific gravity (25°) – 0.860–0.865<br />

Optical rotation – Above –12°0<br />

Refractive index (25°) – About 1.4621<br />

Camphor content – Below 1.5%<br />

Linalool content<br />

Yellow camphor oil:<br />

– 85–90%<br />

This is a by-product of brown camphor oil after the separation of safrole.<br />

Boiling range – 215–225°C<br />

Specific gravity (15°) – 0.97–0.99<br />

Optical rotation – 1°0 to 5°0<br />

Refractive index at 20°<br />

Camphor oil from India:<br />

– About 1.5010<br />

Specific gravity (25°C) – 0.9428–0.9436<br />

Refractive index (25°C) – 1.4713–1.4727<br />

Optical rotation – 26° to –29°<br />

Acid number – 2.48–3.125<br />

Ester number – 4.0–5.0<br />

Acetyl value – 21.6<br />

Chemical Composition<br />

Gildemeister and Hoffmann (1925) and subsequently Hiraizumi (1950) made compilations<br />

on the chemical composition of camphor oils. <strong>The</strong> following chemicals have been<br />

listed by the latter worker.<br />

Acids:<br />

Formic acid, acetic acid, propionic acid, isobutyric acid, isovaleric acid, n-caproic acid,<br />

n-caprylic acid, n-enanthic acid, dl-citronellic acid, lauric acid, myristic acid, piperonytic<br />

acid.<br />

Aldehydes:<br />

Acetaldehyde, propionaldehyde, isovaleraldehyde, n-hexaldehyde, furfural, -methyl<br />

furfural, ,-hexanal, pentenylaldehyde, stearic aldehyde, decyclaldehyde, pentadecylaldehyde,<br />

myristic aldehyde, piperonylacrolein.

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