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The genus Cinnamomum

The genus Cinnamomum

The genus Cinnamomum

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Ketones and oxides:<br />

Camphor, piperitone, cineole, 1,4-cineole, safrole, linalool monoxide.<br />

Alcohols:<br />

Camphor Tree 225<br />

l-Linalool, geraniol, citronellol, d-citronellol, d-borneol, cuminyl alcohol, dihydrocuminyl<br />

alcohol, -terpineol, dl--terpineol, l--terpineol, terpinen-1-ol, terpinen-<br />

4-ol.<br />

Phenols and phenol ethers:<br />

Cresol, ethyl phenol, ethyl guaicol methylethyl phenol, carvacrol, eugenol, methyleugenol,<br />

dihydroeugenol, propylpyrocatechol, elemicin, laurol, microl.<br />

Terpenes:<br />

-Pinene, -pinene, camphene, l-camphene, fenchene, phellandrene, dipentene,<br />

l-limonene, p-cymene, d-sabinene, -terpinene, -terpinene, l--thujene.<br />

Sesquiterpenes:<br />

Bisabolene, cadinene, caryophyllene, camphazulone.<br />

Diterpenes:<br />

-Camphorene, -camphorene, ho-sho-diterpene.<br />

Hirota (1956) and Hirota and Horoi (1967) have given the comparative figures of the<br />

composition of unrectified camphor oils found in Table 9.6.<br />

Wan-Yang et al. (1989) conducted a detailed study of the chemical composition of<br />

camphor trees growing in China (Tables 9.7, 9.8). <strong>The</strong>y have analysed 363 essential oil<br />

samples using GC and GC-MS and identified 34 chemical compounds. Depending<br />

upon the predominance of particular chemical compounds they recognised five chemotypes:<br />

camphor-type, linalool-type, cineole type, isonerolidol type and borneol type<br />

(Table 9.9).<br />

Van Khein et al. (1998) studied the chemical segregation of progenies of camphor<br />

trees with high camphor and linalool contents. <strong>The</strong> leaf oil contents were analysed by<br />

Table 9.6 Composition of unrectified camphor oils (%)<br />

Compounds Japan Taiwan China<br />

Monoterpenes 14 7.2 18.9–18.5<br />

Cineole 4.6 4.1 19.0–21.6<br />

Camphor 45.6 39.6 36.8–33.3<br />

Terpenealcohols 9.9 36.8 16.3–9.3<br />

Safrole 18.1 7.8 2.9–0.8<br />

Sesquiterpenes (plus alcohol) 6.2 2.0 6.3–3.0<br />

Others 1.2 2.0 1.7–1.8<br />

Resinous matter 0.4 0.5 1.1–1.7<br />

Source: Hirota and Hiroi, 1967.

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