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	<id>https://www.ecured.cu/index.php?action=history&amp;feed=atom&amp;title=Hexaconazol</id>
	<title>Hexaconazol - Historial de revisiones</title>
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	<link rel="alternate" type="text/html" href="https://www.ecured.cu/index.php?title=Hexaconazol&amp;action=history"/>
	<updated>2026-08-23T13:29:21Z</updated>
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	<entry>
		<id>https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3519761&amp;oldid=prev</id>
		<title>Carlos idict: Texto reemplazado: «&lt;div align=&quot;justify&quot;&gt;» por «»</title>
		<link rel="alternate" type="text/html" href="https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3519761&amp;oldid=prev"/>
		<updated>2019-08-22T16:50:28Z</updated>

		<summary type="html">&lt;p&gt;Texto reemplazado: «&amp;lt;div align=&amp;quot;justify&amp;quot;&amp;gt;» por «»&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #222; text-align: center;&quot;&gt;← Revisión anterior&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #222; text-align: center;&quot;&gt;Revisión del 16:50 22 ago 2019&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l102&quot; &gt;Línea 102:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Línea 102:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|relac3d&amp;#160; &amp;#160; &amp;#160; &amp;#160; &amp;#160;  = &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|relac3d&amp;#160; &amp;#160; &amp;#160; &amp;#160; &amp;#160;  = &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;&amp;lt;div align=&amp;quot;justify&amp;quot;&amp;gt;&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''Hexaconazol o Hexaconazole ''' . El hexaconazol es un producto agroquímico que sirve para controlar enfermedades de plantas. Este fungicida vegetal es perfecto para el conbatir el mildiu polvoroso, roya, sarna.&amp;#160; Su modo de acción es sistémico, protector y curativo. Inhibe la síntesis de ergosterol. Grupo químico conazole, triazol, clorado.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''Hexaconazol o Hexaconazole ''' . El hexaconazol es un producto agroquímico que sirve para controlar enfermedades de plantas. Este fungicida vegetal es perfecto para el conbatir el mildiu polvoroso, roya, sarna.&amp;#160; Su modo de acción es sistémico, protector y curativo. Inhibe la síntesis de ergosterol. Grupo químico conazole, triazol, clorado.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Propiedades Físicas y Químicas==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Propiedades Físicas y Químicas==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;

&lt;!-- diff cache key wiki1:diff::1.12:old-3180589:rev-3519761 --&gt;
&lt;/table&gt;</summary>
		<author><name>Carlos idict</name></author>
		
	</entry>
	<entry>
		<id>https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3180589&amp;oldid=prev</id>
		<title>Mag040702 en 14:40 16 ago 2018</title>
		<link rel="alternate" type="text/html" href="https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3180589&amp;oldid=prev"/>
		<updated>2018-08-16T14:40:51Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;es&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #222; text-align: center;&quot;&gt;← Revisión anterior&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #222; text-align: center;&quot;&gt;Revisión del 14:40 16 ago 2018&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l103&quot; &gt;Línea 103:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Línea 103:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;div align=&amp;quot;justify&amp;quot;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;div align=&amp;quot;justify&amp;quot;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''Hexaconazol o Hexaconazole ''' .&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''Hexaconazol o Hexaconazole ''' &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. El hexaconazol es un producto agroquímico que sirve para controlar enfermedades de plantas. Este fungicida vegetal es perfecto para el conbatir el mildiu polvoroso, roya, sarna&lt;/ins&gt;.&amp;#160; &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Su modo de acción es sistémico, protector y curativo. Inhibe la síntesis de ergosterol. Grupo químico conazole, triazol, clorado.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Ingrediente acyivo &lt;/del&gt;y &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;modo de acción&lt;/del&gt;==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Propiedades Físicas &lt;/ins&gt;y &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Químicas&lt;/ins&gt;==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Sólido blanco, sin olor. Su punto de fusión se encuentra entre los 110 y 112 °C. Es soluble en agua, metanol, acetona, diclorometano, tolueno, acetato de etilo y hexano. Tiene una presión de vapor igual a 1.4x10-7 mmHg a 20 °C.&amp;#160; &lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Destino en el Ambiente==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Destino en el Ambiente==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;El Hexaconazole es moderadamente persistente en suelos aeróbicos y anaeróbicos, así como en cuerpos de agua aeróbicos. Presenta una baja movilidad en los sistemas terrestres, por lo cual su potencial de lixiviación es muy limitado y no se espera que contamine las aguas subterráneas. No es susceptible a la hidrólisis química o a la fototransformación y no se volatiliza desde el agua o suelo húmedo. La degradación microbiana es un proceso de transformación importante para este plaguicida. Su principal producto de transformación es el 1,2,4-triazol, el cual también es persistente en el suelo y tiene mucho mayor movilidad que el compuesto padre. El Hexaconazole tiene un bajo potencial de bioacumulación en la biota.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Recomendaciones de uso&lt;/del&gt;==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Toxicidad y Medio Ambiente&lt;/ins&gt;==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Es moderadamente tóxico para peces y otros organismos acuáticos invertebrados, pero prácticamente no es tóxico para lombrices de tierra, abejas y aves. El 1,2,4-triazol, el principal producto mayoritario de la degradación del Hexaconazole, tiene una toxicidad igual o menor a la del compuesto padre.&amp;#160; &lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Fuentes==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==Fuentes==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;*http://www.plaguicidasdecentroamerica.una.ac.cr/index.php/base-de-datos-menu/312-hexaconazol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;*http://www.plaguicidasdecentroamerica.una.ac.cr/index.php/base-de-datos-menu/312-hexaconazol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Mag040702</name></author>
		
	</entry>
	<entry>
		<id>https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3180579&amp;oldid=prev</id>
		<title>Mag040702: Página creada con «{{Ficha de compuesto químico |nombre            = Hexoconazol |imagen            = Hexoconazole.jpg  |tamaño de imagen  =  |pie de imagen     =  |imagen2           =  |ta...»</title>
		<link rel="alternate" type="text/html" href="https://www.ecured.cu/index.php?title=Hexaconazol&amp;diff=3180579&amp;oldid=prev"/>
		<updated>2018-08-16T14:25:30Z</updated>

		<summary type="html">&lt;p&gt;Página creada con «{{Ficha de compuesto químico |nombre            = Hexoconazol |imagen            = Hexoconazole.jpg  |tamaño de imagen  =  |pie de imagen     =  |imagen2           =  |ta...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Página nueva&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Ficha de compuesto químico&lt;br /&gt;
|nombre            = Hexoconazol&lt;br /&gt;
|imagen            = Hexoconazole.jpg &lt;br /&gt;
|tamaño de imagen  = &lt;br /&gt;
|pie de imagen     = &lt;br /&gt;
|imagen2           = &lt;br /&gt;
|tamaño de imagen2 = &lt;br /&gt;
|pie de imagen2    = &lt;br /&gt;
|IUPAC             =  (RS)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol&lt;br /&gt;
&amp;lt;!-- General --&amp;gt;&lt;br /&gt;
|otros nombres     = Anvil, Hexaconazole, Planete&lt;br /&gt;
|símbolo           = &lt;br /&gt;
|fórmula1          = C14H17Cl2N3O &lt;br /&gt;
|fórmula2          = &lt;br /&gt;
|fórmula3          = &lt;br /&gt;
&amp;lt;!-- Identificadores --&amp;gt;&lt;br /&gt;
|ATC               = &lt;br /&gt;
|ATC0              = &lt;br /&gt;
|ATC1              = &lt;br /&gt;
|CAS               = &lt;br /&gt;
|RTECS             = &lt;br /&gt;
|ChEBI             = &lt;br /&gt;
|ChemSpiderID      = &lt;br /&gt;
|DrugBank          = &lt;br /&gt;
|PubChem           = &lt;br /&gt;
|UNII              = &lt;br /&gt;
&amp;lt;!-- Propiedades físicas --&amp;gt;&lt;br /&gt;
|estado            = &lt;br /&gt;
|apariencia        = &lt;br /&gt;
|dens1             = &lt;br /&gt;
|dens2             = &lt;br /&gt;
|masa              = &lt;br /&gt;
|PFK               = &lt;br /&gt;
|PFC               = &lt;br /&gt;
|PEK               = &lt;br /&gt;
|PEC               = &lt;br /&gt;
|PDK               = &lt;br /&gt;
|PDC               = &lt;br /&gt;
|TCK               = &lt;br /&gt;
|TCC               = &lt;br /&gt;
|PC                = &lt;br /&gt;
|presión vapor     = &lt;br /&gt;
|cristal           = &lt;br /&gt;
|visco             = &lt;br /&gt;
|índice refracción = &lt;br /&gt;
|dieléctrica       = &lt;br /&gt;
|conductividad eléctrica = &lt;br /&gt;
|conductividad térmica   = &lt;br /&gt;
|banda prohibida   = &lt;br /&gt;
&amp;lt;!-- Propiedades químicas --&amp;gt;&lt;br /&gt;
|pKa               = &lt;br /&gt;
|pKb               = &lt;br /&gt;
|sol               = &lt;br /&gt;
|sol otro          = &lt;br /&gt;
|KPS               = &lt;br /&gt;
|mdipolar          = &lt;br /&gt;
&amp;lt;!-- Propiedades farmacológicas --&amp;gt;&lt;br /&gt;
|Biodisp           = &lt;br /&gt;
|Metabolismo       = &lt;br /&gt;
|Exc               = &lt;br /&gt;
|ExcR              = &lt;br /&gt;
|ExcI              = &lt;br /&gt;
|Semivida          = &lt;br /&gt;
|Embarazo          = &lt;br /&gt;
&amp;lt;!-- Bioquímica --&amp;gt;&lt;br /&gt;
|familia           = &lt;br /&gt;
|esencial          = &lt;br /&gt;
|codón             = &lt;br /&gt;
|isoelect          = &lt;br /&gt;
&amp;lt;!-- Termoquímica --&amp;gt;&lt;br /&gt;
|DfH0G             = &lt;br /&gt;
|DfH0L             = &lt;br /&gt;
|DfH0S             = &lt;br /&gt;
|S0G               = &lt;br /&gt;
|S0L               = &lt;br /&gt;
|S0S               = &lt;br /&gt;
|E0                = &lt;br /&gt;
|caloresp          = &lt;br /&gt;
&amp;lt;!-- Peligrosidad --&amp;gt;&lt;br /&gt;
|PInflam           = &lt;br /&gt;
|NFPA704           = &lt;br /&gt;
|TAutoig           = &lt;br /&gt;
|FrasesR           = &lt;br /&gt;
|FrasesS           = &lt;br /&gt;
|FrasesH           = &lt;br /&gt;
|FrasesP           = &lt;br /&gt;
|LExplos           = &lt;br /&gt;
&amp;lt;!-- Riesgos --&amp;gt;&lt;br /&gt;
|riesgo1           = &lt;br /&gt;
|ingestión         = &lt;br /&gt;
|inhalación        = &lt;br /&gt;
|piel              = &lt;br /&gt;
|ojos              = &lt;br /&gt;
|LD50              = &lt;br /&gt;
|más info          = &lt;br /&gt;
&amp;lt;!-- Compuestos relacionados --&amp;gt;&lt;br /&gt;
|relac1n           = &lt;br /&gt;
|relac1d           = &lt;br /&gt;
|relac2n           = &lt;br /&gt;
|relac2d           = &lt;br /&gt;
|relac3n           = &lt;br /&gt;
|relac3d           = &lt;br /&gt;
}}&lt;br /&gt;
&amp;lt;div align=&amp;quot;justify&amp;quot;&amp;gt;&lt;br /&gt;
'''Hexaconazol o Hexaconazole ''' .  &lt;br /&gt;
==Ingrediente acyivo y modo de acción==&lt;br /&gt;
&lt;br /&gt;
==Destino en el Ambiente==&lt;br /&gt;
&lt;br /&gt;
==Recomendaciones de uso==&lt;br /&gt;
&lt;br /&gt;
==Fuentes==&lt;br /&gt;
*http://www.plaguicidasdecentroamerica.una.ac.cr/index.php/base-de-datos-menu/312-hexaconazol&lt;br /&gt;
*http://www2.inecc.gob.mx/sistemas/plaguicidas/pdf/hexaconazole.pdf&lt;br /&gt;
*https://de.wikipedia.org/wiki/Hexaconazol&lt;br /&gt;
*http://icagrochem.com/4-9-hexaconazole/176518/&lt;br /&gt;
*http://formunica.com/hexaconazole-5-c/&lt;br /&gt;
*http://laguiasata.com/producto-hexaconazol-96&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category: Fungicidas]]&lt;/div&gt;</summary>
		<author><name>Mag040702</name></author>
		
	</entry>
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