<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AJPS</journal-id><journal-title-group><journal-title>American Journal of Plant Sciences</journal-title></journal-title-group><issn pub-type="epub">2158-2742</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajps.2017.811182</article-id><article-id pub-id-type="publisher-id">AJPS-79710</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Essential Oils Leaf of &lt;i&gt;Cinnamomum glaucescens&lt;/i&gt; and &lt;i&gt;Cinnamomum verum&lt;/i&gt; from Vietnam
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hoang</surname><given-names>V. Chinh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ngo</surname><given-names>X. Luong</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dau</surname><given-names>B. Thin</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Do</surname><given-names>N. Dai</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tran</surname><given-names>M. Hoi</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Isiaka</surname><given-names>A. Ogunwande</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Hanoi, Vietnam</addr-line></aff><aff id="aff4"><addr-line>Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, Hanoi, Vietnam</addr-line></aff><aff id="aff3"><addr-line>Faculty of Agriculture, Forestry and Fishery, Nghean College of Economics, Vinh City, Vietnam</addr-line></aff><aff id="aff5"><addr-line>Natural Products Research Unit, Department of Chemistry, Faculty of Science, Lagos State University, Lagos, Nigeria</addr-line></aff><aff id="aff2"><addr-line>Faculty of Science Nature, Hong Duc University, Thanh Hoa City, Vietnam</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>daidn23@gmail.com(DND)</email>;<email>isiaka.ogunwande@lasu.edu.ng(IAO)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>12</day><month>10</month><year>2017</year></pub-date><volume>08</volume><issue>11</issue><fpage>2712</fpage><lpage>2721</lpage><history><date date-type="received"><day>13,</day>	<month>April</month>	<year>2017</year></date><date date-type="rev-recd"><day>16,</day>	<month>October</month>	<year>2017</year>	</date><date date-type="accepted"><day>19,</day>	<month>October</month>	<year>2017</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  In this paper, compounds identified in the essential oils obtained by hydrodistillation of the leaves of 
  Cinnamomum glaucescens
   (Nees) Hand.-Mazz
   
  and 
  Cinnamomum verum 
  J.S. Presl (Lauraceae family) of Vietnam origin are reported. The chemical analyses were performed using gas chromatography
  -
  flame ionisation detector (GC-FID) and gas chromatography coupled with mass spectrometry (GC-MS). The significant compounds of C. glaucescens were geraniol (36.2%) and terpinen-4-ol (19.7%). On the other hand, C. verum comprised of linalool (22.0%) and bicyclogermacrene (11.2%). The present results may represent new chemotypes of the essential oils of C. verum and C. glaucescens.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Cinnamomum verum</kwd><kwd> Cinnamomum glaucescens</kwd><kwd>&lt;/i&gt; Essential Oil</kwd><kwd> Terpenes</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Cinnamomum glaucescens (Nees) Hand.-Mazz is an evergreen tree where the buds are enclosed in overlapping scales. The leaves are about 7 - 10 cm long placed on stalks which is about 1 - 2 cm long. The inflorescences are covered with brown hairs. The fruits are 3 cm long [<xref ref-type="bibr" rid="scirp.79710-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref2">2</xref>] . The major compounds present in the fruit oil of C. glaucescens [<xref ref-type="bibr" rid="scirp.79710-ref3">3</xref>] were 1,8-cineole (13%) and methyl cinnamate (14%), while 1,8-cineole (56%) and α-terpineol (10%) were found in the pericarp oil. In another report, methyl (E)-cinnamate (40.5%) and 1,8-cineole (24.5%) were also identified in the fruit oil of C. glaucescens [<xref ref-type="bibr" rid="scirp.79710-ref4">4</xref>] . 1,8-Cineole (43.6%) and elemicin (92.9%) were described in the fruit [<xref ref-type="bibr" rid="scirp.79710-ref5">5</xref>] and leaf [<xref ref-type="bibr" rid="scirp.79710-ref6">6</xref>] oils respectively. The nematicidal, termiticidal, mosquito larvicidal [<xref ref-type="bibr" rid="scirp.79710-ref4">4</xref>] , insecticidal, antifungal, antiaflatoxin, antioxidant [<xref ref-type="bibr" rid="scirp.79710-ref5">5</xref>] and antibacterial [<xref ref-type="bibr" rid="scirp.79710-ref7">7</xref>] activities of essential oils of C. glaucescens have been reported.</p><p>Cinnamomum verum J.S. Presl is an evergreen tree that grows up to 18 m tall. The fruits are black when ripe and surrounded by the enlarged perianth at the base [<xref ref-type="bibr" rid="scirp.79710-ref1">1</xref>] . The various ethanol extracts of C. verum were reported to possessed high analgesic [<xref ref-type="bibr" rid="scirp.79710-ref8">8</xref>] , antifungal [<xref ref-type="bibr" rid="scirp.79710-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref12">12</xref>] , anti-tuberculosis [<xref ref-type="bibr" rid="scirp.79710-ref13">13</xref>] , antioxidant [<xref ref-type="bibr" rid="scirp.79710-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref15">15</xref>] and antihyperglycaemic [<xref ref-type="bibr" rid="scirp.79710-ref16">16</xref>] properties. 2-Methoxycinnamaldehyde, a component of C. verum was described as a potential anticancer agent [<xref ref-type="bibr" rid="scirp.79710-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref18">18</xref>] . The chemical constituents characterized from the methanolic extracts [<xref ref-type="bibr" rid="scirp.79710-ref9">9</xref>] of C. verum were trans-cinnamaldehyde (20.28%), (E)-3-(2-methoxyphenyl)-2-propenoic acid (40.41%) and 4-vinyl benzoic acid (10.54%).</p><p>Various authors have described different main compounds (chemotypes) of essential oils of C. verum. These include eugenol type [<xref ref-type="bibr" rid="scirp.79710-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref22">22</xref>] , safrole type [<xref ref-type="bibr" rid="scirp.79710-ref23">23</xref>] , cinnamaldehyde and isomers type [<xref ref-type="bibr" rid="scirp.79710-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref23">23</xref>] - [<xref ref-type="bibr" rid="scirp.79710-ref29">29</xref>] , (E)-cinnamaldehyde/ eugenol/linalool type [<xref ref-type="bibr" rid="scirp.79710-ref30">30</xref>] , cinnamyl acetate type [<xref ref-type="bibr" rid="scirp.79710-ref31">31</xref>] and benzyl benzoate type [<xref ref-type="bibr" rid="scirp.79710-ref32">32</xref>] . The essential oils of C. verum were reported to displayed antibacterial [<xref ref-type="bibr" rid="scirp.79710-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref36">36</xref>] , nematicidal [<xref ref-type="bibr" rid="scirp.79710-ref31">31</xref>] , antifungal, anti-elastase and anti-keratinase [<xref ref-type="bibr" rid="scirp.79710-ref37">37</xref>] and anti-rot [<xref ref-type="bibr" rid="scirp.79710-ref38">38</xref>] activities. Cinnamaldehyde, one of major compounds of C. verum oil exhibited antibacterial [<xref ref-type="bibr" rid="scirp.79710-ref25">25</xref>] and anthelmintic [<xref ref-type="bibr" rid="scirp.79710-ref39">39</xref>] properties. The biofungicides action [<xref ref-type="bibr" rid="scirp.79710-ref27">27</xref>] and the efficacy of C. verum essential oil as an acaricidal agent against Rhipicephalus microplus larvae was reported [<xref ref-type="bibr" rid="scirp.79710-ref32">32</xref>] . The oil had a protective effect on experimental Streptococcosis iniae infection in tilapia [<xref ref-type="bibr" rid="scirp.79710-ref29">29</xref>] . Moreover, the oil showed mosquito knock-down and adulticidal activities against Culex quinquefasciatus [<xref ref-type="bibr" rid="scirp.79710-ref40">40</xref>] .</p><p>In the present paper, the results of our studied on the phytochemicals in the essential oils of Vietnamese species of C. verum and C. glaucescens were reported. Previously, the phytochemical constituents of some other plants have been characterized and reported [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] .</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Plant Samples</title><p>The leaf samples of C. glaucescens and C. verum were collected from Bến En National park, Thanh H&#243;a Province, Vietnam, in August 2013. Voucher specimens HVC 377 and HVC 04 respectively were deposited at the HN, Vietnam. The drying of the plant samples was accomplished by exposure to air under laboratorys shade for two weeks.</p></sec><sec id="s2_2"><title>2.2. Hydrodistillation of Essential Oils</title><p>Aliquots of 500 g air-dried and pulverized samples individually subjected to hydrodistillation process which was carried out in an all glass Clevenger-type distillation unit designed according to the established specification [<xref ref-type="bibr" rid="scirp.79710-ref43">43</xref>] . The distillation time was 3 h and conducted at normal pressure. The volatile oils distilled over water and were collected in the receiver arm of the apparatus into clean and previously weighed sample bottles. The oils were kept under refrigeration (4˚C) until the moment of analyses as previously described [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] .</p></sec><sec id="s2_3"><title>2.3. Gas Chromatography (GC) Analysis</title><p>The GC analysis was carried out on HP 6890 Plus Gas chromatograph (Agilent Technologies) equipped with a flame ionization detector (FID). The column used was HP-5MS column with the dimension 30 m &#215; 0.25 mm (film thickness 0.25 mm). Temperature programming parameters: column oven―40˚C, injection pot―250˚C, detector―300˚C. Time programming: 40˚C for 2 min, temperature raised to 220˚C (10 min hold) at 4˚C/min. Carrier gas used was H<sub>2</sub> (flow rate of 1 mL/min), split ratio 10:1, volume injected―1.0 mL. Inlet pressure was 6.1 kPa. Retention indices (RI) value of each component was determined relative to the retention times of a homologous n-alkane series (C<sub>4</sub>-C<sub>32</sub>) with linear interpolation on the HP-5MS column. Relative percentage amounts were computed from GC peak areas without FID response factor correction as previously described [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] .</p></sec><sec id="s2_4"><title>2.4. Gas Chromatography/Mass Spectrometry (GC/MS) Analysis</title><p>The GC/MS experiment was performed on Mass spectrometer (HP 5973 MSD) combined with HP 6890N Plus GC. The system was fitted with HP-5 MS capillary column of 30 m &#215; 0.25 mm having film thickness of 0.25 mm. All operating conditions were similar to that of GC except that He (1 mL/min) was the carrier gas. The Mass Spectrometer was operated on the following conditions: ionization voltage (70 eV), emission current (40 mA) and acquisitions scan (mass range of 35 - 350 amu). The sampling rate was 1.0 scan/s as previously described [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] .</p></sec><sec id="s2_5"><title>2.5. Identification of Constituents of Essential Oils</title><p>The compounds present in the oil samples were identified by comparing the individual relative retention indices with standards obtained from pure compounds. In addition, comparison was made with values from literature under the similar experimental conditions [<xref ref-type="bibr" rid="scirp.79710-ref44">44</xref>] and as previously described [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] .</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><p>The percentage yields of essentials oils obtained from the extraction processes were 0.42% (v/w, C. glaucescens) and 0.45% (v/w, C. verum). The colours of the essential oils were determined as light yellow. The compounds that were identified in the samples could be seen in <xref ref-type="table" rid="table1">Table 1</xref> with detailed analysis of their retention indices and percentage compositions. Monoterpene hydrocarbons (25.9%) and oxygenated monoterpenes (64.3%) were determined as the dominant class of compounds of C. glaucescens oil. the main constituents of the oil were geraniol</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Volatile compounds present in the essential oils of C. galucescens and C. verum</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle" >Compounds<sup>a</sup></th><th align="center" valign="middle" >RI (Cal.)</th><th align="center" valign="middle" >RI (Lit.)</th><th align="center" valign="middle" >C. galucescens</th><th align="center" valign="middle" >C. verum</th></tr></thead><tr><td align="center" valign="middle" >Tricylene</td><td align="center" valign="middle" >926</td><td align="center" valign="middle" >921</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >α-Thujene</td><td align="center" valign="middle" >930</td><td align="center" valign="middle" >926</td><td align="center" valign="middle" >3.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >α-Pinene</td><td align="center" valign="middle" >939</td><td align="center" valign="middle" >932</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0.5</td></tr><tr><td align="center" valign="middle" >Camphene</td><td align="center" valign="middle" >953</td><td align="center" valign="middle" >946</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >2.5</td></tr><tr><td align="center" valign="middle" >Sabinene</td><td align="center" valign="middle" >976</td><td align="center" valign="middle" >964</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0.4</td></tr><tr><td align="center" valign="middle" >β-Myrcene</td><td align="center" valign="middle" >990</td><td align="center" valign="middle" >988</td><td align="center" valign="middle" >0.7</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >α-Phellandrene</td><td align="center" valign="middle" >1006</td><td align="center" valign="middle" >1004</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >0.5</td></tr><tr><td align="center" valign="middle" >α-Terpinene</td><td align="center" valign="middle" >1017</td><td align="center" valign="middle" >1014</td><td align="center" valign="middle" >0.9</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >O-cymene</td><td align="center" valign="middle" >1024</td><td align="center" valign="middle" >1020</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.5</td></tr><tr><td align="center" valign="middle" >Limonene</td><td align="center" valign="middle" >1032</td><td align="center" valign="middle" >1024</td><td align="center" valign="middle" >5.2</td><td align="center" valign="middle" >3.5</td></tr><tr><td align="center" valign="middle" >(Z)-β-Ocimene</td><td align="center" valign="middle" >1044</td><td align="center" valign="middle" >1032</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >1.0</td></tr><tr><td align="center" valign="middle" >(E)-β-Ocimene</td><td align="center" valign="middle" >1052</td><td align="center" valign="middle" >1044</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >γ-Terpinene</td><td align="center" valign="middle" >1061</td><td align="center" valign="middle" >1056</td><td align="center" valign="middle" >1.6</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >trans-Sabinene hydrate</td><td align="center" valign="middle" >10766</td><td align="center" valign="middle" >1073</td><td align="center" valign="middle" >0.8</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Linalool oxide</td><td align="center" valign="middle" >1080</td><td align="center" valign="middle" >1079</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >α-Terpinolene</td><td align="center" valign="middle" >1090</td><td align="center" valign="middle" >1089</td><td align="center" valign="middle" >0.6</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Linalool</td><td align="center" valign="middle" >1100</td><td align="center" valign="middle" >1095</td><td align="center" valign="middle" >1.6</td><td align="center" valign="middle" >22</td></tr><tr><td align="center" valign="middle" >allo-Ocimene</td><td align="center" valign="middle" >1128</td><td align="center" valign="middle" >1128</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.4</td></tr><tr><td align="center" valign="middle" >Terpinen-1-ol</td><td align="center" valign="middle" >1139</td><td align="center" valign="middle" >1134</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >trans-Pinocarveol</td><td align="center" valign="middle" >1146</td><td align="center" valign="middle" >1142</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >Borneol</td><td align="center" valign="middle" >1167</td><td align="center" valign="middle" >1167</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Terpinen-4-ol</td><td align="center" valign="middle" >1177</td><td align="center" valign="middle" >1177</td><td align="center" valign="middle" >19.7</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >α-Terpineol</td><td align="center" valign="middle" >1189</td><td align="center" valign="middle" >1187</td><td align="center" valign="middle" >0.9</td><td align="center" valign="middle" >1.4</td></tr><tr><td align="center" valign="middle" >Verbenone</td><td align="center" valign="middle" >1205</td><td align="center" valign="middle" >1204</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >trans-Piperitol</td><td align="center" valign="middle" >1210</td><td align="center" valign="middle" >1208</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >trans-Carveol</td><td align="center" valign="middle" >1217</td><td align="center" valign="middle" >1217</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >(Z)-2-Decenal</td><td align="center" valign="middle" >1253</td><td align="center" valign="middle" >1265</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Geraniol</td><td align="center" valign="middle" >1259</td><td align="center" valign="middle" >1267</td><td align="center" valign="middle" >36.2</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Geranila</td><td align="center" valign="middle" >1270</td><td align="center" valign="middle" >1269</td><td align="center" valign="middle" >1.6</td><td align="center" valign="middle" >0.4</td></tr><tr><td align="center" valign="middle" >Bornyl acetate</td><td align="center" valign="middle" >1289</td><td align="center" valign="middle" >1287</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >(Z)-Citral</td><td align="center" valign="middle" >1318</td><td align="center" valign="middle" >1318</td><td align="center" valign="middle" >0.5</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Bicycloelemene</td><td align="center" valign="middle" >1327</td><td align="center" valign="middle" >1337</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Eugenol</td><td align="center" valign="middle" >1353</td><td align="center" valign="middle" >1359</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >α-Copaene</td><td align="center" valign="middle" >1377</td><td align="center" valign="middle" >1374</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Geranyl acetate</td><td align="center" valign="middle" >1381</td><td align="center" valign="middle" >1378</td><td align="center" valign="middle" >2.4</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >β-Elemene</td><td align="center" valign="middle" >1391</td><td align="center" valign="middle" >1387</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >α-Gurjunene</td><td align="center" valign="middle" >1407</td><td align="center" valign="middle" >1401</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Methyl eugenol</td><td align="center" valign="middle" >1412</td><td align="center" valign="middle" >1410</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >β-Caryophyllene</td><td align="center" valign="middle" >1419</td><td align="center" valign="middle" >1417</td><td align="center" valign="middle" >0.9</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" >α-Santalene</th><th align="center" valign="middle" >1420</th><th align="center" valign="middle" >1424</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >1.0</th></tr></thead><tr><td align="center" valign="middle" >γ-Elemene</td><td align="center" valign="middle" >1437</td><td align="center" valign="middle" >1434</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >α-Humulene</td><td align="center" valign="middle" >1454</td><td align="center" valign="middle" >1452</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >Germacrene D</td><td align="center" valign="middle" >1485</td><td align="center" valign="middle" >1484</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >α-Amorphene</td><td align="center" valign="middle" >1485</td><td align="center" valign="middle" >1485</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >β-Selinene</td><td align="center" valign="middle" >1486</td><td align="center" valign="middle" >1486</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Eudesma-4,11-diene</td><td align="center" valign="middle" >1490</td><td align="center" valign="middle" >1489</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >Bicyclogermacrene</td><td align="center" valign="middle" >1500</td><td align="center" valign="middle" >1500</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >11.2</td></tr><tr><td align="center" valign="middle" >α-Muurolene</td><td align="center" valign="middle" >1500</td><td align="center" valign="middle" >1501</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.5</td></tr><tr><td align="center" valign="middle" >β-Bisabolene</td><td align="center" valign="middle" >1506</td><td align="center" valign="middle" >1503</td><td align="center" valign="middle" >0.5</td><td align="center" valign="middle" >7.7</td></tr><tr><td align="center" valign="middle" >(E,E)-α-Farnesene</td><td align="center" valign="middle" >1508</td><td align="center" valign="middle" >1505</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.0</td></tr><tr><td align="center" valign="middle" >g-Cadinene</td><td align="center" valign="middle" >1514</td><td align="center" valign="middle" >1512</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >4.0</td></tr><tr><td align="center" valign="middle" >b-Himachalene</td><td align="center" valign="middle" >1518</td><td align="center" valign="middle" >1515</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >δ-Cadinene</td><td align="center" valign="middle" >1525</td><td align="center" valign="middle" >1522</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >1.2</td></tr><tr><td align="center" valign="middle" >Selina-4(15), 7(11)-diene</td><td align="center" valign="middle" >1534</td><td align="center" valign="middle" >1534</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Calacorene</td><td align="center" valign="middle" >1546</td><td align="center" valign="middle" >1544</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Elemol</td><td align="center" valign="middle" >1550</td><td align="center" valign="middle" >1548</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.7</td></tr><tr><td align="center" valign="middle" >(E)-Nerolidol</td><td align="center" valign="middle" >1563</td><td align="center" valign="middle" >1561</td><td align="center" valign="middle" >0.6</td><td align="center" valign="middle" >1.3</td></tr><tr><td align="center" valign="middle" >Spathulenol</td><td align="center" valign="middle" >1578</td><td align="center" valign="middle" >1577</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.0</td></tr><tr><td align="center" valign="middle" >Caryophyllene oxide</td><td align="center" valign="middle" >1583</td><td align="center" valign="middle" >1581</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >5.6</td></tr><tr><td align="center" valign="middle" >Longiborneol</td><td align="center" valign="middle" >1599</td><td align="center" valign="middle" >1597</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >α-Guaiol</td><td align="center" valign="middle" >1600</td><td align="center" valign="middle" >1601</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.8</td></tr><tr><td align="center" valign="middle" >β-Oplopenone</td><td align="center" valign="middle" >1608</td><td align="center" valign="middle" >1607</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.5</td></tr><tr><td align="center" valign="middle" >Caryophyllenol</td><td align="center" valign="middle" >1611</td><td align="center" valign="middle" >1610</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >β-Eudesmol</td><td align="center" valign="middle" >1651</td><td align="center" valign="middle" >1651</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >α-Cadinol</td><td align="center" valign="middle" >1654</td><td align="center" valign="middle" >1652</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.0</td></tr><tr><td align="center" valign="middle" >cis-a-Santalol</td><td align="center" valign="middle" >1677</td><td align="center" valign="middle" >1677</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3.3</td></tr><tr><td align="center" valign="middle" >Valerenol</td><td align="center" valign="middle" >1711</td><td align="center" valign="middle" >1711</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >b-Santalol</td><td align="center" valign="middle" >1713</td><td align="center" valign="middle" >1715</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >Farnesol</td><td align="center" valign="middle" >1718</td><td align="center" valign="middle" >1722</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Benzyl benzoate</td><td align="center" valign="middle" >1760</td><td align="center" valign="middle" >1759</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >95.5</td><td align="center" valign="middle" >90.8</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Monoterpene hydrocarbons</td><td align="center" valign="middle" >25.9</td><td align="center" valign="middle" >12.5</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Oxygenated monoterpenes</td><td align="center" valign="middle" >64.3</td><td align="center" valign="middle" >29.5</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sesquiterpene hydrocarbons</td><td align="center" valign="middle" >3.8</td><td align="center" valign="middle" >30.0</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Oxygenated sesquiterpenes</td><td align="center" valign="middle" >1.3</td><td align="center" valign="middle" >18.8</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Non-terpenes</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap></table-wrap-group><p><sup>a</sup>Compounds order of elution from HP-5MS column; RI (cal.)<sup> </sup>Calculated retention indices of each compounds on HP-5MS column; RI (Lit.)<sup> </sup>Literature retention indices; -not identified.</p><p>(36.2%) and terpinen-4-ol (19.7%). α-Pinene (6.0%), sabinene (6.0%) and limonene (5.2%). Sesquiterpne compounds were present in amount &lt; 1%. Except for α-terpineol, all other known compounds such as 1,8-cineole and methyl cinnamate [<xref ref-type="bibr" rid="scirp.79710-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref5">5</xref>] , α-terpineol [<xref ref-type="bibr" rid="scirp.79710-ref3">3</xref>] , (E)-cinnamate [<xref ref-type="bibr" rid="scirp.79710-ref4">4</xref>] and elemicin [<xref ref-type="bibr" rid="scirp.79710-ref6">6</xref>] that were previously identified in the essential oil of C. glaucescens were not present in the present oil sample. On the other hand, the present oil sample contained large quantities of geraniol and terpinen-4-ol which were not identified in previously studied oil samples of C. glaucescens.</p><p>In the present study, sesquiterpene hydrocarbons (30.0%), oxygenated monoterpenes (29.5%), oxygenated sesquiterpenes (18.8%) and monoterpene hydrocarbons (12.5%) were the classes of compounds present in C. verum. The major constituents of the oil were mainly linalool (22.0%) and bicyclogermacrene (11.2%). Additionally, β-bisabolene (7.7%), caryophyllene oxide (5.6%) and g-cadinene (4.0%) were also present in the oil in significant amount.</p><p>A comparative analysis of the present oil of C. verum and previous studies [<xref ref-type="bibr" rid="scirp.79710-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref32">32</xref>] indicated great variations in their chemical compositions. Several of the compounds that were present in the previously investigated oil samples were not identified in the present oil sample and vice versa. For example, the present oil of C. verum contained lower quantity of eugenol and benzyl benzoate when compared with previous results [<xref ref-type="bibr" rid="scirp.79710-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref32">32</xref>] . In addition, compounds such as (E)-cinnamaldehyde [<xref ref-type="bibr" rid="scirp.79710-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref30">30</xref>] and cinnamyl acetate [<xref ref-type="bibr" rid="scirp.79710-ref31">31</xref>] that were described previously as main compounds of C. veum oil, were not obtained in the oil sample. However, the amount of linalool in the present C. veum oil was in agreement with previously investigated oil sample [<xref ref-type="bibr" rid="scirp.79710-ref31">31</xref>] . A noteworthy observation is that bicyclogermacrene, a main compound in the present C. veum oil was not described to be a significant compound in previously investigated samples of C. verum oils.</p><p>Several reports describing the chemical compositions of essential oils from some Vietnamese species of Cinnamomum have been published. In summary, each of the essential oils possessed compounds that were different from the other oil samples. The main compounds in the essential oil of C. sericans [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] were spathulenol (14.5%) and caryophyllene oxide (9.3%), while ρ-cymene (15.6%), limonene (13.9%) and α-phellandrene (9.2%) were found C. durifolium [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] . However, bicyclogermacrene (33.9%) and β-caryophyllene (25.5%) make up the composition of C. magnificum [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] . The essential oil of C. iners [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] consisted mainly of β-caryophyllene (35.9%) and caryophyllene oxide (12.6%). The leaf oil of C. curvifolium contained high contents of benzyl cinnamate and benzyl benzoate [<xref ref-type="bibr" rid="scirp.79710-ref42">42</xref>] . Interestingly, a-selinene ((24.5%) and β-caryophyllene (23.0%) were the major volatiles of C. rigidifloim [<xref ref-type="bibr" rid="scirp.79710-ref42">42</xref>] .</p><p>From the chemotaxonomy point of view, C. verum in the present study contained linalool which was also found to be the dominant compound of essential oils of C. damhaensis and C. cambodianum from Vietnam [<xref ref-type="bibr" rid="scirp.79710-ref42">42</xref>] . However, the essential oils of most Cinnamomum species from Vietnam possessed low content of (E)-cinnamaldehyde [<xref ref-type="bibr" rid="scirp.79710-ref41">41</xref>] [<xref ref-type="bibr" rid="scirp.79710-ref42">42</xref>] when compared with other samples analyzed from other parts of the world.</p></sec><sec id="s4"><title>4. Conclusion</title><p>The paper reported the compounds identified in the essential oils of C. verum and C. glaucescens grown in Vietnam. The significant compounds of C. glaucescens were geraniol and terpinen-4-ol whil, C. verum comprised of linalool and bicyclogermacrene. In addition, a comparative analysis of the composition of the essential oils was performed with results from other species reported from Vietnam as well as Cinnamomum plants grown in other parts of the world. More studied will be required in order to be able to delineate the various chemotypes of essential oils of Cinnamomum plants in various parts of the world.</p></sec><sec id="s5"><title>Acknowledgements</title><p>Authors are grateful to Mrs. Musilimat Ogunwande for the typesetting of the manuscript.</p></sec><sec id="s6"><title>Cite this paper</title><p>Chinh, H.V., Luong, N.X., Thin, D.B., Dai, D.N., Hoi, T.M. and Ogunwande, I.A. (2017) Essential Oils Leaf of Cinnamomum glaucescens and Cinnamomum verum from Vietnam. American Journal of Plant Sciences, 8, 2712-2721. https://doi.org/10.4236/ajps.2017.811182</p></sec></body><back><ref-list><title>References</title><ref id="scirp.79710-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Jackson, J.K. (1994) Manual of Afforestation in Nepal. 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