<?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.2020.118088</article-id><article-id pub-id-type="publisher-id">AJPS-102214</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>
 
 
  Component Composition of Essential Oils &lt;i&gt;Curcuma longa&lt;/i&gt; L. (Zingiberaceae) Introduced in Uzbekistan
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dilnoza</surname><given-names>I. Sotiboldieva</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Trobjon</surname><given-names>X. Mahkamov</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>National University of Uzbekistan, Tashkent, Uzbekistan</addr-line></aff><aff id="aff2"><addr-line>Institute of Botany, Academy Sciences Republic of Uzbekistan, Tashkent, Uzbekistan</addr-line></aff><pub-date pub-type="epub"><day>03</day><month>08</month><year>2020</year></pub-date><volume>11</volume><issue>08</issue><fpage>1247</fpage><lpage>1253</lpage><history><date date-type="received"><day>7,</day>	<month>July</month>	<year>2020</year></date><date date-type="rev-recd"><day>14,</day>	<month>August</month>	<year>2020</year>	</date><date date-type="accepted"><day>17,</day>	<month>August</month>	<year>2020</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>
 
 
  This article presents the results of studying the component composition of essential oils of leaves and rhizomes of 
  C. 
  longa
   grown in Uzbekistan. The chemical composition of essential oils of vegetative organs of the 
  Curcuma 
  longa
   (Zingiberaceae) plant introduced in Uzbekistan was studied for the first time. Essential oils of the plant were isolated by hydrodistillation, their chemical composition was studied by chromatography-mass spectrometry. In the composition of essential oils of leaves and rhizomes 
  C. 
  longa
   L., introduced in the Tashkent oasis, found 27 and 16 components, respectively, among which 
  the leaf is dominated by α-fellandren (33.79%), α-terpinolene (24.28%), 
  n
  -cymene (12.27%), eucalyptol (9.77%), and in the rhizomes
  -
  6-(1,3-dimeth
  yl-buta-1,3-dienyl)-1,5,5-trimethyl-7-oxa-bicyclo [4.1.0] hept-2-EN (22.77%), α-curcumene (4.11%), 2,6,6,9-tetramethyl-tricyclo [5.4.0.0(2.8)] undec-9-EN (3.81%), α-zedren (1.14%), as well as 3 components that were not identified (the mass spectrum did not match the library data) their mass fraction was 47.47%, 10.41% and 3.46%. The composition of leaves and rhizomes of C. longa differ quantitatively and in quality. For example, α
  -
  curcumene in percentage content is more contained in rhizomes, and α-fellandren, which is the dominant content in leaves, is not found in the underground part.
 
</p></abstract><kwd-group><kwd>Leaf</kwd><kwd> Rhizomes</kwd><kwd> Hydrodistillation</kwd><kwd> Glass Flask</kwd><kwd> Clevenger Nozzle</kwd><kwd> Chemical Composition</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The search for rational ways to introduce food plants into medical practice and obtain medicines based on them is one of the trends in the development of modern medical and pharmaceutical science. The reasons for this trend are, first, the discovery of pharmacological activity for many food plants, and secondly, their low toxicity and the study of almost all possible side effects associated with the fact that food plants have been used by humans for many millennia [<xref ref-type="bibr" rid="scirp.102214-ref1">1</xref>].</p><p>The family of Zingiber&#225;ceae includes 49 genera and 1300 species of perennial herbaceous plants, of which the most widely used in medical practice are representatives of the genus ginger (up to 90 species), turmeric (80 species), cardamom (7 species). The genus of Curcuma (Curcuma L.) belongs to the division Magnoliophyta, class Liliopsida, subclass Liliidae, superorder Zingiberanae, order Zingiberales, family Zingiberaceae, tribe Hedychieae [<xref ref-type="bibr" rid="scirp.102214-ref2">2</xref>].</p></sec><sec id="s2"><title>2. Materials and Method</title><p>The object of study was the rhizomes of Curcuma longa L. (Zingiberaceae), brought from Indonesia in 2017 and grown in the Botanical garden of the National University of Uzbekistan.</p><p>Essential oils from leaves and rhizomes were obtained by hydrodistillation from air-dry raw materials for 3 hours using a glass flask and a Clevenger attachment. The resulting essential oils from both parts of Curcuma longa L. is a pale yellow mobile liquid with a specific smell. Before analysis, essential oils were stored at 0˚C in sealed ampoules to preserve the component composition.</p><p>The obtained essential oils were analyzed using an Agilent 5975C inert MSD/7890AGC chromatographic mass spectrometer. To separate the components of the mixture, Agilent HP-INNOWax quartz capillary column (30 m &#215; 250 μm &#215; 0.25 μm) was used in temperature mode: 50˚C (1 min) - 4˚C/ min to 200˚C (6 min) - 15˚C/min to 250˚C (15 min). The sample was introduced at 1.0 μl (by volume), which the flow rate of the mobile phase was 1.1 ml/min.</p><p>The temperature of the injector is 220˚С. EI-MS spectra were obtained in the m/z range of 10 - 550 AU. the Components were identified by comparing the characteristics of mass spectra with data from electronic libraries (Wiley Registry of Mass Spectral Data-9th Ed., NIST Mass Spectral Library, 2011), and comparing the retention indices (RI) of compounds determined with respect to the retention time of a mixture of n-alkanes (С<sub>9 </sub>- С<sub>28</sub>).</p></sec><sec id="s3"><title>3. Result and Discussion</title><p>Curcuma longa L., Sp. Pl. 1: 2 (1753)—perennial herbaceous plant from the family of Zingiberaceae (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The rhizome is tuberous, almost round, yellowish-gray, up to 4 cm in diameter, with annular scars from dead leaves. From the apical bud of the rhizome, above-ground shoots are formed. From the lateral buds develop underground, relatively short (3 - 10 cm long and 0.5 - 1 cm in diameter) cylindrical shoots. The color of the rhizomes on the outside is yellow-orange to yellow-brown; the fracture is even, reddish-yellow or yellow.</p><p>In addition, numerous thin roots extend from the tuberous rhizome. The leaves are elongated-oval, 20 - 40 cm long, 6 - 15 cm wide, narrowly pointed at</p><p>the top; their base gradually turns into a petiole that is the same length as the leaf plate or slightly shorter than it. The peduncle emerges from the leaf sheaths that cover it high. The inflorescence is a cylindrical spike, 10 - 15 cm long. Bracts in the lower part of the spike are broadly ovate-rounded, ash-green, in the upper part they are ovate or narrowly ovate, pinkish. The calyx is greenish-white, with three blunt teeth. The corolla tube is 1.5 cm long, funnel-shaped in the upper part. The petals are yellow. Fruits are filmy globular boxes. It reproduces mainly by rhizome processes [<xref ref-type="bibr" rid="scirp.102214-ref2">2</xref>].</p><p>All parts of the plant contain a noticeable amount of essential oil. The rhizomes and stems of many species in this genus contain essential oils and yellow dyes (curcumin) and are cultivated as spices and medicinal plants. The most common spice is turmeric long (C. longa) (other names—turmeric home (C. domestica), turmeric), a powder of dried roots, which is known as the spice turmeric. In countries such as China, India, and Malasia, turmeric has been used as a spice in food since ancient times, as well as in folk medicine [<xref ref-type="bibr" rid="scirp.102214-ref3">3</xref>]. According to foreign researchers, BAS contained in rhizomes have antitumor, anti-inflammatory, choleretic, wound-healing effects, etc. [<xref ref-type="bibr" rid="scirp.102214-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref5">5</xref>]. Extracts from turmeric also exhibit analgesic, antioxidant, antiseptic, antispasmodic, dissolving, bactericidal, choleretic effects [<xref ref-type="bibr" rid="scirp.102214-ref6">6</xref>]. Currently, the scientific world’s interest in this plant is increasing every year, research is mainly focused on proving the pharmacological activity of turmeric in relation to oncopathology, mental disorders [<xref ref-type="bibr" rid="scirp.102214-ref7">7</xref>].</p><p>The main active substances are curcuminoids, and three dominant ones are distinguished from them: curcumin, desmethoxycurcumin and bisdemethoxycurcumin; a certain contribution is made by the terpenoid complex of the plant [<xref ref-type="bibr" rid="scirp.102214-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref9">9</xref>].</p><p>The exact geographical origin of turmeric is unknown, but it is safe to assume that it may be South-east Asia [<xref ref-type="bibr" rid="scirp.102214-ref10">10</xref>]. There is no conclusive evidence that C. longa is native to India, although several species of turmeric have been found in India [<xref ref-type="bibr" rid="scirp.102214-ref11">11</xref>]. The greatest variety of turmeric species is found in India, Myanmar, and Thailand [<xref ref-type="bibr" rid="scirp.102214-ref12">12</xref>].</p><p>Despite taxonomic research by taxonomists starting with C. Linnaeus, J. Hooker, A. Rendle, T. Valeton, J. Hatchinson, and G. Watt [<xref ref-type="bibr" rid="scirp.102214-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.102214-ref17">17</xref>], the classification and nomenclature of turmeric remained quite confusing. J. Hooker [<xref ref-type="bibr" rid="scirp.102214-ref14">14</xref>] described turmeric under the natural order Scitamineae and the tribe Zingibereae. However, A. Rendle [<xref ref-type="bibr" rid="scirp.102214-ref15">15</xref>] introduced the subfamily Zingiberoideae in the family Zingiberaceae and described turmeric under the tribe Hedychieae, which was confirmed by J. Hutchinson [<xref ref-type="bibr" rid="scirp.102214-ref17">17</xref>]. It is assumed that the classification of R. Holtum [<xref ref-type="bibr" rid="scirp.102214-ref18">18</xref>] of the family Zingiberaceae is the most authoritative to date, in which it divided the family into two subfamilies, namely Zingiberoideae and Costoideae, and Curcuma was included in the Zingiberoideae as part of the tribe Hedychieae [<xref ref-type="bibr" rid="scirp.102214-ref12">12</xref>].</p><p>Rhizomes of Curcuma, which are widely known in Uzbekistan as a spice, are also a valuable source of biologically active compounds (BAC) with a variety of pharmacological activity [<xref ref-type="bibr" rid="scirp.102214-ref5">5</xref>]. The component composition of essential oils of leaves and rhizomes of C. longa in Uzbekistan has not been studied. This determines the relevance and novelty of our research.</p><p>The purpose of our research is to study the component composition of essential oils of leaves and rhizomes of C. longa grown in Uzbekistan.</p><p>The results of spectral analysis of the obtained essential oils are shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>According to the data presented in <xref ref-type="table" rid="table1">Table 1</xref> in the composition of essential oils of leaves and rhizomes C. longa L., introduced in the Tashkent oasis, found 27 and 16 components, respectively, among which the leaf is dominated by α-fellandren (33.79%), α-terpinolene (24.28%), p-cymene (12.27%), eucalyptol (9.77%), and in the rhizomes-6-(1,3-dimethyl-buta-1,3-dienyl)-1,5,5-trimethyl-7-oxa-bicyclo [4.1.0] hept-2-EN (22.77%), α-curcumene (4.11%), 2,6,6,9-tetramethyl-tricyclo[5.4.0.0(2.8)]undec-9-EN (3.81%), α-zedren (1.14%), as well as 3 components that were not identified (the mass spectrum did not match the library data), their mass fraction was 47.47%, 10.41% and 3.46%.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Component composition of essential oils of leaves and rhizomes of Curcuma longa L. (1-leaf, 2-rhizomes)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >№</th><th align="center" valign="middle" >The name of the component</th><th align="center" valign="middle" >RI*</th><th align="center" valign="middle" >RT**</th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >β-Pinen</td><td align="center" valign="middle" >1097</td><td align="center" valign="middle" >3.257</td><td align="center" valign="middle" >0.61</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >Sabinen</td><td align="center" valign="middle" >1108</td><td align="center" valign="middle" >3.472</td><td align="center" valign="middle" >0.45</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >(+)-2-Karen</td><td align="center" valign="middle" >1116</td><td align="center" valign="middle" >3.626</td><td align="center" valign="middle" >0.24</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3-Karen</td><td align="center" valign="middle" >1131</td><td align="center" valign="middle" >3.927</td><td align="center" valign="middle" >1.47</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >α-Fellandren</td><td align="center" valign="middle" >1152</td><td align="center" valign="middle" >4.345</td><td align="center" valign="middle" >33.79</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >n-Mentha-1,4(8)-dien</td><td align="center" valign="middle" >1153</td><td align="center" valign="middle" >4.347</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.05</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >α-Terpinen</td><td align="center" valign="middle" >1161</td><td align="center" valign="middle" >4.505</td><td align="center" valign="middle" >1.68</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >D-Limonen</td><td align="center" valign="middle" >1179</td><td align="center" valign="middle" >4.868</td><td align="center" valign="middle" >3.01</td><td align="center" valign="middle" >0.04</td></tr><tr><td align="center" valign="middle" >9</td><td align="center" valign="middle" >Evkaliptol (1,8-Sineol)</td><td align="center" valign="middle" >1190</td><td align="center" valign="middle" >5.083</td><td align="center" valign="middle" >9.77</td><td align="center" valign="middle" >0.37</td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >1,5,5-Trimetil-6-metilen-siklogeksen</td><td align="center" valign="middle" >1196</td><td align="center" valign="middle" >5.194</td><td align="center" valign="middle" >0.03</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >11</td><td align="center" valign="middle" >Allosimen</td><td align="center" valign="middle" >1218</td><td align="center" valign="middle" >5.686</td><td align="center" valign="middle" >0.18</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >12</td><td align="center" valign="middle" >γ-Terpinen</td><td align="center" valign="middle" >1225</td><td align="center" valign="middle" >5.852</td><td align="center" valign="middle" >1.60</td><td align="center" valign="middle" >0.02</td></tr><tr><td align="center" valign="middle" >13</td><td align="center" valign="middle" >Kamfen</td><td align="center" valign="middle" >1234</td><td align="center" valign="middle" >6.067</td><td align="center" valign="middle" >0.39</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >14</td><td align="center" valign="middle" >n-Simen</td><td align="center" valign="middle" >1250</td><td align="center" valign="middle" >6.454</td><td align="center" valign="middle" >12.27</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >15</td><td align="center" valign="middle" >α-Terpinolen</td><td align="center" valign="middle" >1267</td><td align="center" valign="middle" >6.854</td><td align="center" valign="middle" >24.28</td><td align="center" valign="middle" >1.20</td></tr><tr><td align="center" valign="middle" >16</td><td align="center" valign="middle" >m-Simen</td><td align="center" valign="middle" >1392</td><td align="center" valign="middle" >10.328</td><td align="center" valign="middle" >0.21</td><td align="center" valign="middle" >0.08</td></tr><tr><td align="center" valign="middle" >17</td><td align="center" valign="middle" >Digidro-n-simen</td><td align="center" valign="middle" >1406</td><td align="center" valign="middle" >10.728</td><td align="center" valign="middle" >0.43</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >18</td><td align="center" valign="middle" >2,3-Dixlopropen</td><td align="center" valign="middle" >1410</td><td align="center" valign="middle" >10.834</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.11</td></tr><tr><td align="center" valign="middle" >19</td><td align="center" valign="middle" >4-Metil-3-(1-metiletiliden)-siklogeksen</td><td align="center" valign="middle" >1526</td><td align="center" valign="middle" >14.220</td><td align="center" valign="middle" >0.90</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >транс-Kariofillen</td><td align="center" valign="middle" >1555</td><td align="center" valign="middle" >15.083</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.82</td></tr><tr><td align="center" valign="middle" >21</td><td align="center" valign="middle" >o-Simen</td><td align="center" valign="middle" >1568</td><td align="center" valign="middle" >15.474</td><td align="center" valign="middle" >0.35</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >22</td><td align="center" valign="middle" >транс-α-Bisabolen</td><td align="center" valign="middle" >1622</td><td align="center" valign="middle" >17.063</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.13</td></tr><tr><td align="center" valign="middle" >23</td><td align="center" valign="middle" >3-Etil-o-ksilol</td><td align="center" valign="middle" >1627</td><td align="center" valign="middle" >17.196</td><td align="center" valign="middle" >0.02</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >24</td><td align="center" valign="middle" >2-Etil-м-ksilol</td><td align="center" valign="middle" >1652</td><td align="center" valign="middle" >17.885</td><td align="center" valign="middle" >0.36</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >25</td><td align="center" valign="middle" >R(+)-Limonen</td><td align="center" valign="middle" >1664</td><td align="center" valign="middle" >18.223</td><td align="center" valign="middle" >0.63</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >26</td><td align="center" valign="middle" >Bisiklo[4.2.0]okta-1,3,5-tien-7-ol</td><td align="center" valign="middle" >1725</td><td align="center" valign="middle" >19.932</td><td align="center" valign="middle" >0.04</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >27</td><td align="center" valign="middle" >n-Mentha-1,3,8-trien</td><td align="center" valign="middle" >1767</td><td align="center" valign="middle" >21.113</td><td align="center" valign="middle" >0.93</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >28</td><td align="center" valign="middle" >1,6-Dmetilgepta-1,3,5-триен</td><td align="center" valign="middle" >1780</td><td align="center" valign="middle" >21.475</td><td align="center" valign="middle" >0.20</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >29</td><td align="center" valign="middle" >Izopropenil toluol</td><td align="center" valign="middle" >1806</td><td align="center" valign="middle" >22.367</td><td align="center" valign="middle" >1.88</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >30</td><td align="center" valign="middle" >n-Mentha-1,5,8-trien</td><td align="center" valign="middle" >1829</td><td align="center" valign="middle" >23.744</td><td align="center" valign="middle" >0.05</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >31</td><td align="center" valign="middle" >α-Sedren</td><td align="center" valign="middle" >2013</td><td align="center" valign="middle" >30.245</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.14</td></tr><tr><td align="center" valign="middle" >32</td><td align="center" valign="middle" >α-Kurkumen</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >30.963</td><td align="center" valign="middle" >0.85</td><td align="center" valign="middle" >4.11</td></tr><tr><td align="center" valign="middle" >33</td><td align="center" valign="middle" >Not identified</td><td align="center" valign="middle" >2021</td><td align="center" valign="middle" >31.678</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >47.47</td></tr><tr><td align="center" valign="middle" >34</td><td align="center" valign="middle" >Not identified</td><td align="center" valign="middle" >2030</td><td align="center" valign="middle" >33.375</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >10.41</td></tr><tr><td align="center" valign="middle" >35</td><td align="center" valign="middle" >6-(1,3-Dimetil-Buta-1,3-dienil)-1,5,5-trimetil-7-oksa-bisiklo [4.1.0] gept-2-en</td><td align="center" valign="middle" >2032</td><td align="center" valign="middle" >33.738</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >22.77</td></tr><tr><td align="center" valign="middle" >36</td><td align="center" valign="middle" >Not identified</td><td align="center" valign="middle" >2049</td><td align="center" valign="middle" >36.671</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3.46</td></tr><tr><td align="center" valign="middle" >37</td><td align="center" valign="middle" >2,6,6,9-Tetrametil-trisiklo[5.4.0.0(2,8)] undek-9-en</td><td align="center" valign="middle" >2061</td><td align="center" valign="middle" >38.841</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3.81</td></tr><tr><td align="center" valign="middle"  colspan="4"  >S</td><td align="center" valign="middle" >96.62</td><td align="center" valign="middle" >95.99</td></tr></tbody></table></table-wrap><p>Note: RI*-Kovac Index; RT**-holding Time.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Based on the data, it can be seen that the composition of leaves and rhizomes of C. longa differ quantitatively and in quality. For example, α-curcumene in percentage content is more contained in rhizomes, and α-fellandren, which is the dominant content in leaves, is not found in the underground part.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Sotiboldieva, D.I. and Mahkamov, T.X. (2020) Component Composition of Essential Oils Curcuma longa L. (Zingiberaceae) Introduced in Uzbekistan. American Journal of Plant Sciences, 11, 1247-1253. https://doi.org/10.4236/ajps.2020.118088</p></sec></body><back><ref-list><title>References</title><ref id="scirp.102214-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Degtyareva, I.I., Skopichenko, S.V. and Skrypnik, I.N. 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