<?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.2014.521330</article-id><article-id pub-id-type="publisher-id">AJPS-50399</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>
 
 
  Comparison and Quantification of the Development of Phenolic Compounds during the Aging of Cacha&#231;a in Oak (Quercus sp) and Amburana (Amburana cearensis) Barrels
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ilder</surname><given-names>D. Santiago</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>Maria</surname><given-names>das G. Cardoso</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>Juliana</surname><given-names>de A. Santiago</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>Marcos</surname><given-names>S. Gomes</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>Leonardo</surname><given-names>M. A. Rodrigues</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>Rafaela</surname><given-names>M. Brandão</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>Rodolfo</surname><given-names>R. Cardoso</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>Gabriel</surname><given-names>B. d’Avila</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>Bruno</surname><given-names>L. da Silva</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>Alex</surname><given-names>R. S. Caetano</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Chemistry, Federal University of Lavras, Lavras, Brazil</addr-line></aff><aff id="aff2"><addr-line>Department of Food Science, Federal University of Lavras, Lavras, Brazil</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>mcardoso@dqi.ufla.br(MDGC)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>10</day><month>10</month><year>2014</year></pub-date><volume>05</volume><issue>21</issue><fpage>3140</fpage><lpage>3150</lpage><history><date date-type="received"><day>22</day>	<month>August</month>	<year>2014</year></date><date date-type="rev-recd"><day>22</day>	<month>September</month>	<year>2014</year>	</date><date date-type="accepted"><day>5</day>	<month>October</month>	<year>2014</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>
 
 
  Aging is a stage of the cacha
  &amp;ccedila production process in which several chemical reactions occur between compounds extracted from the wood and other compounds present on the beverage. In an attempt to establish a profile regarding the chemical characterization of aged cacha
  &amp;ccedilas, phenolic compounds have been studied because of the specific characteristics of each wood species and their known antioxidant properties. This work sought to assess and compare the development of 12 phenolic compounds in cacha
  &amp;ccedilas aged in oak (
  <em>Quercus sp</em>) and amburana (
  <em>Amburana cearenses</em>) barrels during a period of 12 months. There was a progressive increase in the concentration of phenolic compounds in the beverage for both of the types of wood. The principal compounds encountered in the cacha
  &amp;ccedila aged in oak barrels were gallic acid, syringaldehyde and syringic acid, while vanillic acid, syringaldehyde, sinapic acid and gallic acid were isolated from that aged in amburana barrels.
 
</p></abstract><kwd-group><kwd>Beverage</kwd><kwd> Aging</kwd><kwd> Phenolic Compounds</kwd><kwd> Liquid Chromatography</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Aging of alcoholic beverages is a common practice among producers that try to increase the value to their prod- ucts, making them more competitive in the market [<xref ref-type="bibr" rid="scirp.50399-ref1">1</xref>] . Aging is responsible for improving organoleptic charac- teristics of cacha&#231;a, making its flavor more pleasant and mild. Some substances from the wood are incorporated into the beverage during aging [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] . In Brazil, most of the cacha&#231;a producers are small-scale producers, and a great variety of wood species may be used for aging [<xref ref-type="bibr" rid="scirp.50399-ref3">3</xref>] .</p><p>Although oak (Quercus sp) is the wood traditionally used for aging alcoholic beverages, several other types of native Brazilian wood species have been employed in the manufacture of barrels for aging cacha&#231;a, such as pea- nut (Plerogyne nitens), amburana (Amburana cearensis), cedar (Cedrela fissilis), jatob&#225; (Hymenaeae carbouril), ip&#234; (Tabebuia sp), freij&#243; (Cordia goeldiana), garapa (Apuleia leiocarpa), balm (Myroxylon peruiferum), yellow mahogany (Plathynemia foliosa) and jequitib&#225; (Carinian legalis) [<xref ref-type="bibr" rid="scirp.50399-ref4">4</xref>] . This practice has developed because of the high cost of oak, which is a wood typical of the Northern hemisphere [<xref ref-type="bibr" rid="scirp.50399-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref6">6</xref>] .</p><p>Among the several types of native Brazilian wood species, a species that has been studied with respect to the aging of cacha&#231;a is amburana (Amburana cearensis), which belongs to the Leguminoseae Papilonoideae (Faba- ceae) family and is commonly known as amburana, imburana-de-cheiro and cumaru [<xref ref-type="bibr" rid="scirp.50399-ref7">7</xref>] . Although it is consi- dered to be a native of the northeastern backlands, the occurrence of A. cearenses may be observed in nearly all of South America (from Peru to Argentina). It is a leafy tree that may attain a height of 15 m, with white flowers, flattened pod and brownish-red bark. It has a pleasant odor that is conferred by the presence of coumarins [<xref ref-type="bibr" rid="scirp.50399-ref8">8</xref>] .</p><p>The main reactions that occur during the aging process are reactions among secondary compounds obtained from distillation, direct extraction of wood components, decomposition of the wood macromolecules (cellulose, hemicellulose and lignin) and the subsequent incorporation of these compounds into the beverage. Furthermore, reactions may occur among the wood compounds and the original compounds of the distilled beverage [<xref ref-type="bibr" rid="scirp.50399-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref10">10</xref>] .</p><p>The main compounds extracted from wood by the distillates are volatile oils, phenolic compounds, tannic substances, sugars, glycerol and non-volatile organic acids. Among them, the importance of studying phenolic compounds in aged cacha&#231;as because of the value of antioxidant compounds for human health should be high- lighted [<xref ref-type="bibr" rid="scirp.50399-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref12">12</xref>] .</p><p>Several studies have assessed the chemical and sensorial quality of aged beverages. Many aldehydes and phe- nolic acids have been found in distilled alcoholic beverages aged in oak barrels, such as vanillin, syringaldehyde, coniferaldehyde and sinapaldehyde, which were apparently formed by the acid alcoholysis of lignin. Other phe- nolic acids that have been identified are gallic acid, p-hydroxybenzoic acid, p-coumaric acid, cinnamic acid, va- nillic acid and syringic acid [<xref ref-type="bibr" rid="scirp.50399-ref13">13</xref>] .</p><p>High-performance liquid chromatography with UV-Vis detectors is widely cited in the literature for the detec- tion of phenolic compounds in beverages [<xref ref-type="bibr" rid="scirp.50399-ref14">14</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref17">17</xref>] . In addition to HPLC, other techniques are used, such as gas chromatography, capillary electrophoresis (CE), ultraviolet detection, electrochemistry, and fluorescent and mass spectrometries [<xref ref-type="bibr" rid="scirp.50399-ref18">18</xref>] . This work sought to compare the development of 12 phenolic compounds in cacha&#231;as aged during a period of 12 months in oak (Quercus sp) and amburana (Amburana cearensis) barrels using HPLC with UV-Vis detection.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Sample Collection</title><p>The samples were produced in a commercial alembic located in the municipality of Perd&#245;es, Minas Gerais, Bra- zil during the harvest of 2011. Distillation was performed in a copper alembic. The cacha&#231;a was aged in oak (Quercus sp) and amburana (Amburana cearensis) barrels, both having a capacity of 200 L, and 130 L of beve- rage was stored in each barrel. The barrels were kept in closed sheds with controlled temperature and air humid- ity. They were positioned horizontally to provide a greater contact between the beverage and the wood, and the barrels were distanced from one another to avoid gas exchange. Two-liter aliquots were collected each month during 12 months and sent for the analyses of phenolic compounds. The analyses were performed at the La- borat&#243;rio de Qualidade de Aguardentes, Departamento de Qu&#237;mica (DQI), Universidade Federal de Lavras (UFLA).</p></sec><sec id="s2_2"><title>2.2. Chromatographic Analysis</title><p>Chromatographic analyses were performed on a Shimadzu HPLC equipped with two model SPD-M20A high- pressure pumps, a model DGU-20A3 degasser, a model CBM-20A interface, a model SIL-10AF automatic in- jector and a diode array detector (DAD). The column employed was an Agilent-Zorbax Eclipse XDB-C18 (4.6 &#215; 250 mm, 5 &#181;m) connected to an Agilent-Zorbax Eclipse XDB-C18 4-Pack (4.6 &#215; 12.5 mm, 5 &#181;m) pre-column.</p><p>The 12 phenolic compounds in cacha&#231;as aged in oak and amburana barrels were analyzed according to the method proposed by Anjos [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] .<sup> </sup>The phenolic compounds were gallic acid, catechin, vanillic acid, phenol, syrin- gic acid, vanillin, syringaldehyde, p-coumaric acid, sinapic acid, coumarin, 4-methylumbelliferone and o-cou- maric acid. The standards for these compounds were acquired from Sigma-Aldrich or Acros Organics. The sol- vents employed in the mobile phase were HPLC grade: methanol (Merck) and glacial acetic acid (J. T. Baker) and water type I obtained from a Milli-Q system.</p><p>External standardization was used for quantification. To construct the analytical curves, dilutions were per- formed with an intermediate solution containing a mixture of all the standards, which was obtained by means of the dilution of previously prepared stock solutions. This intermediate solution contained the following concen- trations of the standards: gallic acid (6.80 mg∙L<sup>−1</sup>), catechin (11.61 mg∙L<sup>−1</sup>), vanillic acid (6.73 mg∙L<sup>−1</sup>), phenol (3.76 mg∙L<sup>−1</sup>), syringic acid (7.93 mg∙L<sup>−1</sup>), vanillin (6.08 mg∙L<sup>−1</sup>), syringaldehyde (7.29 mg∙L<sup>−1</sup>), p-coumaric acid (6.56 mg∙L<sup>−1</sup>), sinapic acid (8.97 mg∙L<sup>−1</sup>), coumarin (5.85 mg∙L<sup>−1</sup>), 4-methylumbelliferone (7.05 mg∙L<sup>−1</sup>) and o-coumaric acid (6.56 mg∙L<sup>−1</sup>).</p><p>The solutions of 2% acetic acid in water (Solvent A) and methanol: water: acetic acid (70:28:2% v/v) (Solvent B) were used as the mobile phase for eluting the compounds. Samples and standards were eluted using the fol- lowing gradients: from 0 to 25 min (0% - 40% B); 25 - 40 min (40% - 55% B); 40 - 50 min (55% - 100% B); 50 - 60 min (100% - 0% B). The wavelength employed was 280 nm, the flow rate was 0.8 mg∙L<sup>−1</sup>, and the<sup> </sup>volume injected was 20 &#181;L.</p><p>Samples and standards were filtered through a 0.45-&#181;m polyethylene membrane (Millipore) and injected di- rectly into the chromatographic system. Injections of standards and samples were performed in triplicates. The identities of the analytes were confirmed using the retention times, and the profiles of sample peaks were com- pared with those of the standards.</p><p>To guarantee the analytical quality of the results, procedures were performed to validate the method, which was assessed according to the following parameters: selectivity, linearity, limit of detection, limit of quantifica- tion and accuracy [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] -[<xref ref-type="bibr" rid="scirp.50399-ref19">19</xref>] . The selectivity was determined through the use of a fresh cacha&#231;a (without contact with wood). Initially, an analysis of this cacha&#231;a, to which the standards were added, was performed. The ma- thematical relationship between the sign and the concentration of the species of interest was expressed by means of the line equations (analytical curves) and their respective determination coefficients (R<sup>2</sup>).</p><p>The limits of detection and quantification of the methods were estimated using the parameters of the analyti- cal curve according to the mathematical equations: LD = 3 &#215; (s/S) and LQ = 10 &#215; (s/S), in which s is the esti- mate of the standard deviation of the equation for the regression line, and S is the angular coefficient of the ana- lytical curve. The accuracy was assessed by means of recovery assays using three randomly chosen samples that were fortified with analyte standards at three different concentrations. The recovery was determined by consi- dering the results obtained for each analyte using the following mathematical equation: %Recovery = [(meas- ured concentration)/(expected concentration)] &#215; 100 [<xref ref-type="bibr" rid="scirp.50399-ref19">19</xref>] .</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>A completely randomized design (CRD) was used in a scheme of fractions subdivided in the space. The data were submitted to analysis of variance, and the means were compared by the Scott-Knott test at 95% of confi- dence using the statistical software SISVAR [<xref ref-type="bibr" rid="scirp.50399-ref20">20</xref>] . A principal component analysis (PCA) was performed to ve- rify possible similarities between the types of wood with respect to the concentrations of phenolic compounds. Results were centered on the mean for posterior analysis, which was accomplished using the CHEMOFACE software [<xref ref-type="bibr" rid="scirp.50399-ref21">21</xref>] .</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><p>The chromatogram of the standard solution of the 12 phenolic compounds obtained through spectrophotometric detection after analysis of 20 μL by HPLC is presented in <xref ref-type="fig" rid="fig1">Figure 1</xref>. The compounds were well separated under the chromatographic conditions employed.</p><p>The mean retention time observed for each compound was: 1) gallic acid (8.754 &#177; 0.433 min); 2) catechin</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Chromatogram of the standard solution of phenolic compounds with spectrophotometric detection. Concentration of each standard: 1.161 &#215; 10<sup>−5</sup> mg∙L<sup>−1</sup></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-2601693x6.png"/></fig><p>(23.961 &#177; 0.107 min); 3) vanillic acid (29.021 &#177; 0.119 min); 4) phenol (29.607 &#177; 0.457 min); 5) syringic acid (31.571 &#177; 0.105 min); 6) vanillin (32.647 &#177; 0.104 min); 7) syringaldehyde (34.721 &#177; 0.135 min); 8) p-coumaric acid (38.085 &#177; 0.349 min); 9) sinapic acid (40.743 &#177; 0.212 min); 10) coumarin (42.294 &#177; 0.962 min); 11) 4-methylumbelliferone (46.843 &#177; 0.126 min); and 12) o-coumaric acid (49.501 &#177; 0.128 min), values that corro- borate with those found by Anjos [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] . In the end of the run, an increase was observed in the base line that may be explained by the presence of oligomers and polymers. In the literature, studies that correlate the phenol con- tents with the use of reversed-phase liquid chromatography relate that the presence of many oligomers and po- lymers of flavan-3-ol results in alterations in the base line of the chromatograms [<xref ref-type="bibr" rid="scirp.50399-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref23">23</xref>] .</p><p>The selectivity of the methods employed was assessed through the comparison between the matrix lacking the substances of interest (phenolic compounds) and the matrix with the analyte standards (<xref ref-type="fig" rid="fig2">Figure 2</xref>). A positive selectivity was observed, because the chromatogram presented a satisfactory separation of the compounds.</p><p>The correlation coefficients ranged from 0.9994 to 0.9999, thus showing a strong linear correlation between the concentrations of the analyzed compounds and the area of the peaks, as recommended in the literature [<xref ref-type="bibr" rid="scirp.50399-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.50399-ref25">25</xref>] . The correlation coefficients, limits of detection and limits of quantification obtained are presented on Ta- ble 1.</p><p>The limits of detection and quantification found for the phenolic compounds ranged from 0.025 to 0.057 mg∙L<sup>−1</sup> and from 0.084 to 0.190 mg∙L<sup>−1</sup>, respectively. These values were inferior to those found by Aquino and Santiago [<xref ref-type="bibr" rid="scirp.50399-ref6">6</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref17">17</xref>] , and were close to those obtained by Anjos and Zacaroni [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref13">13</xref>] . Anjos [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] found values be- tween 0.016 and 0.131 mg∙L<sup>−1</sup> and ranging from 0.055 to 0.437 mg∙L<sup>−1</sup> for the limits of detection and quantifi- cation, respectively. Santiago [<xref ref-type="bibr" rid="scirp.50399-ref17">17</xref>] found limits of detection and quantification ranging from 0.031 to 0.168 mg∙L<sup>−1</sup> and 0.104 to 0.677 mg∙L<sup>−1</sup>, respectively.</p><p>The method employed for the analysis of phenolic compounds in cacha&#231;a aged in wood barrels was shown to be highly sensitive. The differences may be explained by differences in chromatographic conditions, such as the equipment and/or methods adopted for quantifying the compounds [<xref ref-type="bibr" rid="scirp.50399-ref19">19</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref26">26</xref>] .</p><p>The accuracy of the analytical method was assessed by means of recovery assays in which the concentration of phenolic compounds was calculated through the increase of peak areas obtained after the addition of a known amount of standard to three randomly chosen samples [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] . The mean results for the percentage of recovery were 92% for gallic acid, 82% for catechin, 95% for vanillic acid, 90% for phenol, 92% for syringic acid, 96% for vanillin, 93% for syringaldehyde, 94% for p-coumaric acid, 91% for sinapic acid, 95% for coumarin, 96% for 4-methylumbelliferone and 86% for o-coumaric acid.</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Chromatogram of the fresh cacha&#231;a and that fortified with stan- dards of phenolic compounds at the 1.04 &#215; 10<sup>−</sup><sup>5</sup> mol∙L<sup>−1</sup> concentration. Identification of peaks: (1) gallic acid; (2) catechin; (3) vanillic acid; (4) phenol; (5) syringic acid; (6) vanillin; (7) syringaldehyde; (8) p-coumaric acid; (9) sinapic acid; (10) coumarin; (11) 4-methylumbelliferone; and (12) o-coumaric acid</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-2601693x7.png"/></fig><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Parameters, correlation coefficients (r<sup>2</sup>) for the analytical curves, and limits of detection (LD) and quantification (LQ)<sup>*</sup> obtained by the analytical method employed</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Compound</th><th align="center" valign="middle" >b</th><th align="center" valign="middle" >a</th><th align="center" valign="middle" >r<sup>2</sup></th><th align="center" valign="middle" >LD (mg∙L<sup>−1</sup>)</th><th align="center" valign="middle" >LQ (mg∙L<sup>−1</sup>)</th></tr></thead><tr><td align="center" valign="middle" >Gallic acid</td><td align="center" valign="middle" >68463.23</td><td align="center" valign="middle" >−3035.01</td><td align="center" valign="middle" >0.9998</td><td align="center" valign="middle" >0.044</td><td align="center" valign="middle" >0.146</td></tr><tr><td align="center" valign="middle" >Catechin</td><td align="center" valign="middle" >16893.41</td><td align="center" valign="middle" >−671.57</td><td align="center" valign="middle" >0.9999</td><td align="center" valign="middle" >0.057</td><td align="center" valign="middle" >0.190</td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" >44512.01</td><td align="center" valign="middle" >−1041.40</td><td align="center" valign="middle" >0.9995</td><td align="center" valign="middle" >0.035</td><td align="center" valign="middle" >0.116</td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >12042.23</td><td align="center" valign="middle" >−403.83</td><td align="center" valign="middle" >0.9994</td><td align="center" valign="middle" >0.032</td><td align="center" valign="middle" >0.107</td></tr><tr><td align="center" valign="middle" >Syringic acid</td><td align="center" valign="middle" >74757.71</td><td align="center" valign="middle" >−1607.86</td><td align="center" valign="middle" >0.9997</td><td align="center" valign="middle" >0.035</td><td align="center" valign="middle" >0.117</td></tr><tr><td align="center" valign="middle" >Vanillin</td><td align="center" valign="middle" >96068.54</td><td align="center" valign="middle" >−2649.16</td><td align="center" valign="middle" >0.9996</td><td align="center" valign="middle" >0.027</td><td align="center" valign="middle" >0.091</td></tr><tr><td align="center" valign="middle" >Syringaldehyde</td><td align="center" valign="middle" >49814.62</td><td align="center" valign="middle" >−2113.48</td><td align="center" valign="middle" >0.9998</td><td align="center" valign="middle" >0.034</td><td align="center" valign="middle" >0.116</td></tr><tr><td align="center" valign="middle" >p-Coumaric acid</td><td align="center" valign="middle" >116451.88</td><td align="center" valign="middle" >−1282.22</td><td align="center" valign="middle" >0.9994</td><td align="center" valign="middle" >0.025</td><td align="center" valign="middle" >0.084</td></tr><tr><td align="center" valign="middle" >Sinapic acid</td><td align="center" valign="middle" >31456.89</td><td align="center" valign="middle" >−2638.53</td><td align="center" valign="middle" >0.9996</td><td align="center" valign="middle" >0.046</td><td align="center" valign="middle" >0.155</td></tr><tr><td align="center" valign="middle" >Coumarin</td><td align="center" valign="middle" >108863.21</td><td align="center" valign="middle" >−2863.04</td><td align="center" valign="middle" >0.9998</td><td align="center" valign="middle" >0.026</td><td align="center" valign="middle" >0.087</td></tr><tr><td align="center" valign="middle" >4-Methylumbelliferone</td><td align="center" valign="middle" >32840.07</td><td align="center" valign="middle" >1089.44</td><td align="center" valign="middle" >0.9996</td><td align="center" valign="middle" >0.043</td><td align="center" valign="middle" >0.147</td></tr><tr><td align="center" valign="middle" >o-Coumaric acid</td><td align="center" valign="middle" >149391.38</td><td align="center" valign="middle" >−3430.66</td><td align="center" valign="middle" >0.9997</td><td align="center" valign="middle" >0.033</td><td align="center" valign="middle" >0.113</td></tr></tbody></table></table-wrap><p><sup>*</sup>Linear regression: y = bx + a.</p><p>According to Ribani and Collins [<xref ref-type="bibr" rid="scirp.50399-ref19">19</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref26">26</xref>] , the acceptable values of recovery for analyses are between 70 and 120%, with an accuracy of &#177;20%. However, depending on the analytical complexity of the sample, this value may vary from 50% to 120%, with an accuracy of &#177;15%. Thus, according to the results found in the present work for the 12 phenolic compounds studied, the method presented a high recovery, with the mean values rang- ing from 82% to 96%. There are studies in the literature reporting recoveries close to those observed in the cur- rent work [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref13">13</xref>] .<sup> </sup>The results obtained for the quantification of 12 phenolic compounds during the aging of ca- cha&#231;a in oak and amburana barrels are presented on <xref ref-type="table" rid="table2">Table 2</xref> and <xref ref-type="table" rid="table3">Table 3</xref>, respectively.</p><table-wrap-group id="2"><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Concentrations of 12 phenolic compounds (mg∙L<sup>−1</sup>) observed during the aging of cacha&#231;a in oak barrels</title></caption><table-wrap id="2_1"><table><tbody><thead><tr><th align="center" valign="middle" >Aging time (months)</th><th align="center" valign="middle" >0</th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >4</th><th align="center" valign="middle" >5</th><th align="center" valign="middle" >6</th></tr></thead><tr><td align="center" valign="middle" >Compounds</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gallic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.213 &#177; 0.001</td><td align="center" valign="middle" >0.269 &#177; 0.003</td><td align="center" valign="middle" >0.317 &#177; 0.003</td><td align="center" valign="middle" >0.367 &#177; 0.004</td><td align="center" valign="middle" >0.417 &#177; 0.001</td><td align="center" valign="middle" >0.477 &#177; 0.003</td></tr><tr><td align="center" valign="middle" >Catechin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td></tr><tr><td align="center" valign="middle" >Syringic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.138 &#177; 0.001</td><td align="center" valign="middle" >0.169 &#177; 0.001</td><td align="center" valign="middle" >0.190 &#177; 0.001</td><td align="center" valign="middle" >0.221 &#177; 0.001</td></tr><tr><td align="center" valign="middle" >Vanillin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.097 &#177; 0.001</td><td align="center" valign="middle" >0.113 &#177; 0.001</td><td align="center" valign="middle" >0.119 &#177; 0.006</td><td align="center" valign="middle" >0.134 &#177; 0.002</td></tr><tr><td align="center" valign="middle" >Syringaldehyde</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.118 &#177; 0.002</td><td align="center" valign="middle" >0.135 &#177; 0.002</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.177 &#177; 0.005</td><td align="center" valign="middle" >0.210 &#177; 0.006</td><td align="center" valign="middle" >0.231 &#177; 0.004</td></tr><tr><td align="center" valign="middle" >p-Coumaric acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Sinapic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Coumarin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >4-Methylumbelliferone</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td></tr><tr><td align="center" valign="middle" >o-Coumaric acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Sum of each phenolic compound (on each month)</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.331</td><td align="center" valign="middle" >0.404</td><td align="center" valign="middle" >0.552</td><td align="center" valign="middle" >0.826</td><td align="center" valign="middle" >0.936</td><td align="center" valign="middle" >1.063</td></tr></tbody></table></table-wrap><table-wrap id="2_2"><table><tbody><thead><tr><th align="center" valign="middle" >Aging time (months)</th><th align="center" valign="middle" >7</th><th align="center" valign="middle" >8</th><th align="center" valign="middle" >9</th><th align="center" valign="middle" >10</th><th align="center" valign="middle" >11</th><th align="center" valign="middle" >12</th><th align="center" valign="middle" >Evolution/ Times</th></tr></thead><tr><td align="center" valign="middle" >Compounds</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gallic acid</td><td align="center" valign="middle" >0.522 &#177; 0.004</td><td align="center" valign="middle" >0.567 &#177; 0.001</td><td align="center" valign="middle" >0.606 &#177; 0.001</td><td align="center" valign="middle" >0.652 &#177; 0.007</td><td align="center" valign="middle" >0.691 &#177; 0.003</td><td align="center" valign="middle" >0.720 &#177; 0.003</td><td align="center" valign="middle" >3.380</td></tr><tr><td align="center" valign="middle" >Catechin</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Syringic acid</td><td align="center" valign="middle" >0.245 &#177; 0.001</td><td align="center" valign="middle" >0.272 &#177; 0.003</td><td align="center" valign="middle" >0.294 &#177; 0.001</td><td align="center" valign="middle" >0.315 &#177; 0.001</td><td align="center" valign="middle" >0.332 &#177; 0.001</td><td align="center" valign="middle" >0.346 &#177; 0.009</td><td align="center" valign="middle" >2.507</td></tr><tr><td align="center" valign="middle" >Vanillin</td><td align="center" valign="middle" >0.142 &#177; 0.003</td><td align="center" valign="middle" >0.153 &#177; 0.001</td><td align="center" valign="middle" >0.158 &#177; 0.001</td><td align="center" valign="middle" >0.174 &#177; 0.007</td><td align="center" valign="middle" >0.194 &#177; 0.002</td><td align="center" valign="middle" >0.201 &#177; 0.004</td><td align="center" valign="middle" >2.072</td></tr><tr><td align="center" valign="middle" >Syringaldehyde</td><td align="center" valign="middle" >0.250 &#177; 0.001</td><td align="center" valign="middle" >0.279 &#177; 0.002</td><td align="center" valign="middle" >0.301 &#177; 0.001</td><td align="center" valign="middle" >0.323 &#177; 0.001</td><td align="center" valign="middle" >0.334 &#177; 0.001</td><td align="center" valign="middle" >0.346 &#177; 0.012</td><td align="center" valign="middle" >2.932</td></tr><tr><td align="center" valign="middle" >p-Coumaric acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.045 &#177; 0.003</td><td align="center" valign="middle" >0.048 &#177; 0.009</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1.066</td></tr><tr><td align="center" valign="middle" >Sinapic acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.157 &#177; 0.003</td><td align="center" valign="middle" >0.157 &#177; 0.009</td><td align="center" valign="middle" >0.157 &#177; 0.015</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Coumarin</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >4-Methylumbelliferone</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >o-Coumaric acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Sum of each phenolic compound (on each month)</td><td align="center" valign="middle" >1.159</td><td align="center" valign="middle" >1.271</td><td align="center" valign="middle" >1.359</td><td align="center" valign="middle" >1.666</td><td align="center" valign="middle" >1.747</td><td align="center" valign="middle" >1.770</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap></table-wrap-group><p>ND = non-detected;</p><table-wrap-group id="3"><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Concentrations of 12 phenolic compounds (mg∙L<sup>−1</sup>) observed during the aging of cacha&#231;a in amburana barrels</title></caption><table-wrap id="3_1"><table><tbody><thead><tr><th align="center" valign="middle" >Aging time (months)</th><th align="center" valign="middle" >0</th><th align="center" valign="middle" >1</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >4</th><th align="center" valign="middle" >5</th><th align="center" valign="middle" >6</th></tr></thead><tr><td align="center" valign="middle" >Compounds</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gallic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.326 &#177; 0.006</td><td align="center" valign="middle" >0.405 &#177; 0.004</td><td align="center" valign="middle" >0.510 &#177; 0.006</td><td align="center" valign="middle" >0.646 &#177; 0.006</td><td align="center" valign="middle" >0.829 &#177; 0.002</td><td align="center" valign="middle" >1.007 &#177; 0.008</td></tr><tr><td align="center" valign="middle" >Catechin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >1.095 &#177; 0.009<sup>**</sup></td><td align="center" valign="middle" >2.975 &#177; 0.006<sup>**</sup></td><td align="center" valign="middle" >4.089 &#177; 0.004<sup>**</sup></td><td align="center" valign="middle" >4.741 &#177; 0.007<sup>**</sup></td><td align="center" valign="middle" >5.451&#177; 0.050<sup>**</sup></td><td align="center" valign="middle" >6.101 &#177; 0.009<sup>**</sup></td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.112 &#177; 0.004</td><td align="center" valign="middle" >0.226 &#177; 0.003</td><td align="center" valign="middle" >0.255 &#177; 0.012</td><td align="center" valign="middle" >0.333 &#177; 0.001</td><td align="center" valign="middle" >0.389 &#177; 0.014</td><td align="center" valign="middle" >0.451 &#177; 0.002</td></tr><tr><td align="center" valign="middle" >Syringic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.869 &#177; 0.011</td><td align="center" valign="middle" >0.789 &#177; 0.002</td><td align="center" valign="middle" >0.790 &#177; 0.002</td><td align="center" valign="middle" >0.846 &#177; 0.001</td><td align="center" valign="middle" >0.921 &#177; 0.007</td><td align="center" valign="middle" >0.988 &#177; 0.016</td></tr><tr><td align="center" valign="middle" >Vanillin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.098 &#177; 0.001</td><td align="center" valign="middle" >0.090 &#177; 0.006</td><td align="center" valign="middle" >0.084 &#177; 0.003</td><td align="center" valign="middle" >0.081 &#177; 0.001</td><td align="center" valign="middle" >0.103 &#177; 0.003</td><td align="center" valign="middle" >0.113 &#177; 0.002</td></tr><tr><td align="center" valign="middle" >Syringaldehyde</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.805 &#177; 0.004</td><td align="center" valign="middle" >0.744 &#177; 0.002</td><td align="center" valign="middle" >0.806 &#177; 0.005</td><td align="center" valign="middle" >0.927 &#177; 0.005</td><td align="center" valign="middle" >1.092 &#177; 0.002</td><td align="center" valign="middle" >1.304 &#177; 0.006</td></tr><tr><td align="center" valign="middle" >p-Coumaric acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.119 &#177; 0.007</td><td align="center" valign="middle" >0.147 &#177; 0.001</td><td align="center" valign="middle" >0.166 &#177; 0.001</td><td align="center" valign="middle" >0.183 &#177; 0.023</td><td align="center" valign="middle" >0.350 &#177; 0.001</td><td align="center" valign="middle" >0.393 &#177; 0.003</td></tr><tr><td align="center" valign="middle" >Sinapic acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >0.255 &#177; 0.001</td><td align="center" valign="middle" >0.634 &#177; 0.004</td><td align="center" valign="middle" >0.881 &#177; 0.003</td><td align="center" valign="middle" >0.947 &#177; 0.052</td><td align="center" valign="middle" >1.088 &#177; 0.015</td><td align="center" valign="middle" >1.206 &#177; 0.040</td></tr><tr><td align="center" valign="middle" >Coumarin</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >4-Methylumbelliferone</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.254 &#177; 0.015</td><td align="center" valign="middle" >0.334 &#177; 0.012</td><td align="center" valign="middle" >0.503 &#177; 0.005</td><td align="center" valign="middle" >0.511 &#177; 0.019</td></tr><tr><td align="center" valign="middle" >o-Coumaric acid</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.145 &#177; 0.015</td><td align="center" valign="middle" >0.167 &#177; 0.003</td><td align="center" valign="middle" >0.172 &#177; 0.006</td><td align="center" valign="middle" >0.173 &#177; 0.001</td><td align="center" valign="middle" >0.180 &#177; 0.007</td></tr><tr><td align="center" valign="middle" >Sum of each phenolic compound (on each month)</td><td align="center" valign="middle" >ND</td><td align="center" valign="middle" >3.679</td><td align="center" valign="middle" >6.155</td><td align="center" valign="middle" >8.002</td><td align="center" valign="middle" >9.210</td><td align="center" valign="middle" >10.899</td><td align="center" valign="middle" >12.324</td></tr></tbody></table></table-wrap><table-wrap id="3_2"><table><tbody><thead><tr><th align="center" valign="middle" >Aging time (months)</th><th align="center" valign="middle" >7</th><th align="center" valign="middle" >8</th><th align="center" valign="middle" >9</th><th align="center" valign="middle" >10</th><th align="center" valign="middle" >11</th><th align="center" valign="middle" >12</th><th align="center" valign="middle" >Evolution/ Times</th></tr></thead><tr><td align="center" valign="middle" >Compounds</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gallic acid</td><td align="center" valign="middle" >1.188 &#177; 0.004</td><td align="center" valign="middle" >1.372 &#177; 0.005</td><td align="center" valign="middle" >1.528 &#177; 0.002</td><td align="center" valign="middle" >1.661 &#177; 0.008<sup>**</sup></td><td align="center" valign="middle" >1.757 &#177; 0.002<sup>**</sup></td><td align="center" valign="middle" >1.865 &#177; 0.005<sup>**</sup></td><td align="center" valign="middle" >5.721</td></tr><tr><td align="center" valign="middle" >Catechin</td><td align="center" valign="middle" >0.209 &#177; 0.010</td><td align="center" valign="middle" >0.217 &#177; 0.004</td><td align="center" valign="middle" >0.231 &#177; 0.003</td><td align="center" valign="middle" >0.229 &#177; 0.003</td><td align="center" valign="middle" >0.230 &#177; 0.010</td><td align="center" valign="middle" >0.244 &#177; 0.010</td><td align="center" valign="middle" >1.167</td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" >6.574 &#177; 0.046<sup>**</sup></td><td align="center" valign="middle" >7.111 &#177; 0.068<sup>**</sup></td><td align="center" valign="middle" >7.512 &#177; 0.028<sup>**</sup></td><td align="center" valign="middle" >7.857 &#177; 0.023<sup>**</sup></td><td align="center" valign="middle" >8.023 &#177; 0.002<sup>**</sup></td><td align="center" valign="middle" >8.355 &#177; 0.032<sup>**</sup></td><td align="center" valign="middle" >7.630</td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >0.470 &#177; 0.015</td><td align="center" valign="middle" >0.462 &#177; 0.001</td><td align="center" valign="middle" >0.493 &#177; 0.003</td><td align="center" valign="middle" >0.489 &#177; 0.013</td><td align="center" valign="middle" >0.550 &#177; 0.034</td><td align="center" valign="middle" >0.785 &#177; 0.078</td><td align="center" valign="middle" >7.008</td></tr><tr><td align="center" valign="middle" >Syringic acid</td><td align="center" valign="middle" >1.042 &#177; 0.001</td><td align="center" valign="middle" >1.092 &#177; 0.001</td><td align="center" valign="middle" >1.118 &#177; 0.006</td><td align="center" valign="middle" >1.135 &#177; 0.006</td><td align="center" valign="middle" >1.159 &#177; 0.013</td><td align="center" valign="middle" >1.254 &#177; 0.005</td><td align="center" valign="middle" >1.443</td></tr><tr><td align="center" valign="middle" >Vanillin</td><td align="center" valign="middle" >0.125 &#177; 0.002</td><td align="center" valign="middle" >0.140 &#177; 0.005</td><td align="center" valign="middle" >0.147 &#177; 0.001</td><td align="center" valign="middle" >0.155 &#177; 0.001</td><td align="center" valign="middle" >0.157 &#177; 0.001</td><td align="center" valign="middle" >0.156 &#177; 0.004</td><td align="center" valign="middle" >1.592</td></tr><tr><td align="center" valign="middle" >Syringaldehyde</td><td align="center" valign="middle" >1.490 &#177; 0.018</td><td align="center" valign="middle" >1.667 &#177; 0.015</td><td align="center" valign="middle" >1.799 &#177; 0.040</td><td align="center" valign="middle" >1.957 &#177; 0.003<sup>**</sup></td><td align="center" valign="middle" >2.024 &#177; 0.020<sup>**</sup></td><td align="center" valign="middle" >2.226 &#177; 0.002<sup>**</sup></td><td align="center" valign="middle" >2.765</td></tr><tr><td align="center" valign="middle" >p-Coumaric acid</td><td align="center" valign="middle" >0.433 &#177; 0.001</td><td align="center" valign="middle" >0.470 &#177; 0.004</td><td align="center" valign="middle" >0.508 &#177; 0.001</td><td align="center" valign="middle" >0.525 &#177; 0.005</td><td align="center" valign="middle" >0.556 &#177; 0.006</td><td align="center" valign="middle" >0.601 &#177; 0.003</td><td align="center" valign="middle" >5.050</td></tr><tr><td align="center" valign="middle" >Sinapic acid</td><td align="center" valign="middle" >1.262 &#177; 0.036</td><td align="center" valign="middle" >1.384 &#177; 0.029</td><td align="center" valign="middle" >1.498 &#177; 0.034</td><td align="center" valign="middle" >1.806 &#177; 0.026</td><td align="center" valign="middle" >1.761 &#177; 0.050</td><td align="center" valign="middle" >2.577 &#177; 0.040<sup>**</sup></td><td align="center" valign="middle" >10.105</td></tr><tr><td align="center" valign="middle" >Coumarin</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >4-Methylumbelliferone</td><td align="center" valign="middle" >0.707 &#177; 0.059</td><td align="center" valign="middle" >1.076 &#177; 0.010</td><td align="center" valign="middle" >1.263 &#177; 0.002</td><td align="center" valign="middle" >1.363 &#177; 0.025</td><td align="center" valign="middle" >1.566&#177; 0.020</td><td align="center" valign="middle" >1.727&#177; 0.018</td><td align="center" valign="middle" >6.799</td></tr><tr><td align="center" valign="middle" >o-Coumaric acid</td><td align="center" valign="middle" >0.185 &#177; 0.006</td><td align="center" valign="middle" >0.203 &#177; 0.003</td><td align="center" valign="middle" >0.229 &#177; 0.010</td><td align="center" valign="middle" >0.238 &#177; 0.008</td><td align="center" valign="middle" >0.267&#177; 0.002</td><td align="center" valign="middle" >0.256&#177; 0.017</td><td align="center" valign="middle" >1.765</td></tr><tr><td align="center" valign="middle" >Sum of each phenolic compound (on each month)</td><td align="center" valign="middle" >13.685</td><td align="center" valign="middle" >15.194</td><td align="center" valign="middle" >16.326</td><td align="center" valign="middle" >17.415</td><td align="center" valign="middle" >18.050</td><td align="center" valign="middle" >20.049</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap></table-wrap-group><p>ND = non-detected; **Sample diluted (10 times) in 40% ethyl alcohol for the quantification.</p><p>A progressive increase in the concentration of phenolic compounds for each species of wood analyzed was observed. The concentration ranged from 0.331 to 1.770 mg∙L<sup>−1</sup> (for cacha&#231;a aged for 1 to 12 months in oak barrels) and from 3.679 to 20.049 mg∙L<sup>−1</sup> (for cacha&#231;a aged for 1 to 12 months in amburana barrels). It was evi- dent that cacha&#231;a aged in amburana barrels contained higher concentrations of phenolic compounds. Such high concentrations may be explained by morphological differences, time of use and type of pre-treatment of the bar- rel [<xref ref-type="bibr" rid="scirp.50399-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref27">27</xref>] .</p><p>The cacha&#231;a aged in oak barrels contained a predominance of gallic acid, syringic acid and syringaldehyde, results that corroborate those of Anjos and Zacaroni [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] - [<xref ref-type="bibr" rid="scirp.50399-ref13">13</xref>] . The cacha&#231;a aged in amburana barrels contained predomnately gallic acid, vanillic acid, syringaldehyde and sinapic acid. This result differs from that of Santiago [<xref ref-type="bibr" rid="scirp.50399-ref17">17</xref>] , who assessed cacha&#231;a stored in amburana barrels during four months and observed a predominance of ca- techin, syringaldehyde and 4-methylumbelliferone. Generally, there is a progressive increase in the concentra- tion of phenolic compounds in cacha&#231;as stored in different barrels. Despite the complexity of the process, the mechanism of the gradual increase in the content of acids and aldehydes seems to follow the scheme: cinnamic aldehydes (coniferaldehyde and sinapalde&#237;do), benzoic aldehydes (vanillin and syringaldehyde) and benzoic acids (vanillic acid and syringic acid) [<xref ref-type="bibr" rid="scirp.50399-ref2">2</xref>] -[<xref ref-type="bibr" rid="scirp.50399-ref5">5</xref>] . The differences in the composition of phenols were observed in the chro- matograms (<xref ref-type="fig" rid="fig3">Figure 3</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>) of the cacha&#231;as aged in oak and amburana barrels.</p><p>The PC1 &#215; PC2 biplot of loadings and scores in which phenolic compounds of aged cacha&#231;as were related with the types of wood studied is presented in <xref ref-type="fig" rid="fig5">Figure 5</xref>. The PCA showed that it was possible to describe 99.49% of the data with the first and second principal components, from which 98.61% of the total variance was de- scribed by the first component. According to this analysis, all the samples differed with respect to the phenolic compounds throughout the different months of aging and the type of wood used in the process.</p></sec><sec id="s4"><title>4. Conclusion</title><p>The chromatographic method proposed for the determination of 12 phenolic compounds presented acceptable values for all the validation parameters analyzed. A progressive increase was observed with respect to the in- corporation of phenolic compounds during the aging of cacha&#231;a in barrels constructed from both species of wood. The main compounds quantified in the cacha&#231;a aged in the oak barrel were gallic acid, syringaldehyde and syringic acid, and those observed in the cacha&#231;a aged in the amburana barrel were vanillic acid, syringalde- hyde, sinapic acid and gallic acid.</p><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Chromatogram of aged cacha&#231;a on the first and twelfth month of storage in oak barrels. Identification of peaks: (1) gallic acid; (2) catechin; (3) vanillic acid; (4) syringic acid; (5) vanillin; (6) syringaldehyde; (7) p-cou- maric acid; (8) sinapic acid; (9) coumarin; (10) o-coumaric acid</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-2601693x8.png"/></fig><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Chromatogram of aged cacha&#231;a on the first and twelfth month of storage in amburana barrels. Identification of peaks: (1) gallic acid; (2) catechin; (3) vanillic acid; (4) phenol; (5) syringic acid; (6) vanillin; (7) syringaldehyde; (8) p-coumaric acid; (9) acid sinapic; (10) coumarin; (11) 4-methy- lumbelliferone; (12) o-coumaric acid</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-2601693x9.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> PC1 &#215; PC2 biplot of loadings and scores of cacha&#231;as aged in oak and amburana barrels withs respect to the composition of phenolic compounds</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-2601693x10.png"/></fig></sec><sec id="s5"><title>Acknowledgements</title><p>The authors thank the Conselho Nacional de Desenvolvimento Cient&#237;fico e Tecnol&#243;gico (CNPQ), the Funda&#231;&#227;o de Amparo &#224; Pesquisa do Estado de Minas Gerais (FAPEMIG), and the Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior (CAPES) for financial support. We also thank Cacha&#231;a Jo&#227;o Mendes for the valuable contribution and for furnishing the cacha&#231;a samples.</p></sec><sec id="s6"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.50399-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Dias, S.M.B.C., Maia, A.B.R.A. and Nelson, D.L. (2009) Utiliza&amp;ccedil&amp;atildeo de Madeiras Nativas no Envelhecimento da Cacha&amp;ccedila de Alambique. Informe Agropecuário, 30, 49-54.</mixed-citation></ref><ref id="scirp.50399-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Anjos, J.P., Cardoso, M.G., Saczk, A.A., Dorea, H.S., Santiago, W.D., Zacaroni, L.M., Machado, A.M.R. and Nelson, D.L. (2011) Evolution of the Concentration of Phenolic Compounds in Cacha&amp;ccedila during Aging in an Oak (Quercus sp.) Barrel. 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