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		<title>Camphene: Properties, History and Applications</title>
		<link>https://dmg.es/en/camphene-properties-history-and-applications/</link>
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		<dc:creator><![CDATA[dmg_mugasa]]></dc:creator>
		<pubDate>Mon, 17 Aug 2026 08:45:26 +0000</pubDate>
				<category><![CDATA[Aroma Chemicals]]></category>
		<category><![CDATA[Fragrances]]></category>
		<guid isPermaLink="false">https://dmg.es/?p=11165</guid>

					<description><![CDATA[<p>Camphene (CAS 79-92-5) is a bicyclic monoterpene that occurs naturally in the essential oils of plants such as pine, cypress, rosemary, ginger and orange blossoms(neroli). It is an isomer of pinenes (alpha-pinene and beta-pinene) and limonene. Although it shares the same molecular formula (C10H16) with these aromatic chemicals, the arrangement of its molecular structure gives [&#8230;]</p>
<p>La entrada <a href="https://dmg.es/en/camphene-properties-history-and-applications/">Camphene: Properties, History and Applications</a> se publicó primero en <a href="https://dmg.es/en/a-world-full-of-fragrances/">DMG</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p><strong data-start="0" data-end="12">Camphene</strong> (CAS 79-92-5) is a bicyclic monoterpene that occurs naturally in the essential oils of plants such as pine, <a href="https://dmg.es/en/cypress-essential-oil-discovering-its-uses-properties-and-history/">cypress</a>,<a href="https://dmg.es/en/rosemary-essential-oil-history-features-and-benefits/"> rosemary</a>, <a href="https://dmg.es/en/ginger-essential-oil-properties-history-and-uses/">ginger</a> and <a href="https://dmg.es/en/neroli-oil-uses-history-and-fragrance-of-orange-blossom-essence/">orange blossoms(neroli)</a>.</p>
<p>It is an isomer of <strong data-start="517" data-end="528">pinenes</strong> (alpha-pinene and beta-pinene) and <strong data-start="564" data-end="576">limonene</strong>. Although it shares the same molecular formula (C<sub>10</sub>H<sub>16</sub>) with these aromatic chemicals, the arrangement of its molecular structure gives it distinct organoleptic properties and makes it the only member of the group that occurs as a crystalline solid at room temperature, with a <strong data-start="854" data-end="871">melting point</strong> of around 48–52 °C.</p>
<p data-start="893" data-end="1118" data-is-last-node="" data-is-only-node="">Its name derives from the Latin <em data-start="925" data-end="935">camphora</em>, reflecting its <strong data-start="952" data-end="987">close relationship with camphor</strong>, a semi-solid, crystalline aromatic compound that can be produced on an industrial scale through the oxidation of camphene itself.</p>
<figure id="attachment_2373" aria-describedby="caption-attachment-2373" style="width: 197px" class="wp-caption aligncenter"><img decoding="async" class="wp-image-2373" src="https://dmg.es/wp-content/uploads/2020/02/Canfeno-300x268.png" alt="" width="197" height="176" srcset="https://dmg.es/wp-content/uploads/2020/02/Canfeno-300x268.png 300w, https://dmg.es/wp-content/uploads/2020/02/Canfeno.png 361w" sizes="(max-width: 197px) 100vw, 197px" /><figcaption id="caption-attachment-2373" class="wp-caption-text">Chemical structure of camphene (C10H16)</figcaption></figure>
<p>&nbsp;</p>
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<p data-start="0" data-end="209" data-is-last-node="" data-is-only-node="">Camphene has an <strong data-start="16" data-end="63">intense balsamic and woody aromatic profile</strong>, with <strong data-start="70" data-end="98">fresh, penetrating notes</strong> that are widely used in <strong data-start="123" data-end="157">perfumery, cosmetics, air care</strong> and <strong data-start="162" data-end="182">food flavourings</strong>, among other applications.</p>
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<th style="border: 1px solid #ddd; padding: 10px; background: #2E7D32; color: #ffffff; text-align: center;">AROMATIC PROFILE</th>
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<td style="border: 1px solid #ddd; padding: 10px; text-align: center;"><strong>Camphoraceous · Woody · Balsamic · Fresh · Herbal · Pungent · Piney · Resinous · Earthy</strong></td>
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<p>In nature, it contributes to the classic scent of damp pine needles that can be perceived when walking through dense coniferous forests in the early morning.</p>
<p>&nbsp;</p>
<h2>Camphene Production Methods</h2>
<p class="PDq2pG_selectionAnchorContainer" data-start="0" data-end="220">Although camphene can be obtained by <strong data-start="37" data-end="75">extraction from the essential oils</strong> that contain it, its concentration in these oils is generally low, making this method unviable for meeting the high levels of industrial demand.</p>
<p data-start="222" data-end="439" data-is-last-node="" data-is-only-node="">For this reason, camphene is currently produced mainly through the <strong data-start="289" data-end="328">catalytic isomerization of α-pinene</strong>, a monoterpene that is abundant in <strong data-start="364" data-end="378">turpentine</strong>, a <strong data-start="382" data-end="413">100% renewable raw material</strong> obtained from pine resin.</p>
<figure id="attachment_11157" aria-describedby="caption-attachment-11157" style="width: 433px" class="wp-caption aligncenter"><img fetchpriority="high" decoding="async" class="wp-image-11157" src="https://dmg.es/wp-content/uploads/2026/08/Resina-pino-1024x575.jpg" alt="" width="433" height="243" srcset="https://dmg.es/wp-content/uploads/2026/08/Resina-pino-1024x575.jpg 1024w, https://dmg.es/wp-content/uploads/2026/08/Resina-pino-300x169.jpg 300w, https://dmg.es/wp-content/uploads/2026/08/Resina-pino-768x431.jpg 768w, https://dmg.es/wp-content/uploads/2026/08/Resina-pino-800x450.jpg 800w, https://dmg.es/wp-content/uploads/2026/08/Resina-pino.jpg 1280w" sizes="(max-width: 433px) 100vw, 433px" /><figcaption id="caption-attachment-11157" class="wp-caption-text">Conifer Resin</figcaption></figure>
<p>&nbsp;</p>
<p>This process is an excellent example of <strong data-start="40" data-end="59">green chemistry</strong>, making use of a <strong data-start="77" data-end="110">sustainable forestry resource</strong> without relying on petrochemical sources.</p>
<p>&nbsp;</p>
<h2>A Brief History of Camphene</h2>
<p class="PDq2pG_selectionAnchorContainer" data-start="0" data-end="118">The history of camphene is closely linked to the search for alternatives to whale oil as a fuel for domestic lighting.</p>
<p data-start="120" data-end="270" data-is-last-node="" data-is-only-node="">In the 1830s, <strong data-start="134" data-end="152">camphine lamps</strong> began to gain popularity. These oil lamps predated kerosene lamps and were designed to burn <strong data-start="245" data-end="269">rectified turpentine</strong>.</p>
<figure id="attachment_11159" aria-describedby="caption-attachment-11159" style="width: 302px" class="wp-caption aligncenter"><img decoding="async" class="wp-image-11159" src="https://dmg.es/wp-content/uploads/2026/08/Camphene-Lamp.jpg" alt="" width="302" height="434" srcset="https://dmg.es/wp-content/uploads/2026/08/Camphene-Lamp.jpg 356w, https://dmg.es/wp-content/uploads/2026/08/Camphene-Lamp-209x300.jpg 209w" sizes="(max-width: 302px) 100vw, 302px" /><figcaption id="caption-attachment-11159" class="wp-caption-text"><strong>Camphine or Camphene Lamp, 19th century.</strong><br />Watercolor and graphite illustration by Jacob Gielens (1938).<br />Public domain (NoC US 1.0).<br />Source: National Gallery of Art, Washington, D.C.</figcaption></figure>
<p>&nbsp;</p>
<p class="PDq2pG_selectionAnchorContainer" data-start="0" data-end="176">In the English-speaking world, this fuel was also marketed under the name <em data-start="74" data-end="88"><strong data-start="75" data-end="87">camphene</strong></em>, a term that is now used for camphene in English and derives from the Latin <em data-start="165" data-end="175">camphora</em>.</p>
<p data-start="178" data-end="449">The widespread use of turpentine and its derivatives prompted 19th-century chemists to study its composition in depth. It was in this context that <strong data-start="325" data-end="348">Marcellin Berthelot</strong> eventually isolated, characterized and formally named <strong data-start="403" data-end="415">camphene</strong> as the pure molecule known today.</p>
<p data-start="451" data-end="836" data-is-last-node="" data-is-only-node="">Berthelot was also the scientist who demonstrated in 1870 that <strong data-start="514" data-end="567">authentic camphor could be obtained from camphene</strong>. This discovery represented a major advance in organic chemistry and paved the way for the subsequent development of methods to produce this valuable compound without the need to import the expensive natural variety extracted from the Asian tree <em data-start="814" data-end="835">Cinnamomum camphora</em>.</p>
<p>&nbsp;</p>
<h2>Camphene Applications in Modern Industry</h2>
<p class="PDq2pG_selectionAnchorContainer" data-start="0" data-end="162">Today, due to its olfactory profile, camphene is used directly in <strong data-start="66" data-end="79">perfumery</strong> to provide pine-needle nuances and as a <strong data-start="120" data-end="140">flavouring agent</strong> in the food industry.</p>
<p data-start="164" data-end="417">It is also highly relevant to industry as a <strong data-start="208" data-end="224">raw material</strong>, serving as an intermediate in the industrial synthesis of <a class="decorated-link" href="https://dmg.es/borneol-propiedades-historia-y-aplicaciones/" target="_new" rel="noopener" data-start="284" data-end="358"><strong data-start="285" data-end="296">borneol</strong></a>, <strong data-start="360" data-end="393">isoborneol, isobornyl acetate</strong> and <strong data-start="398" data-end="409">camphor</strong> itself.</p>
<p data-start="419" data-end="602">Another application of camphene is the <strong data-start="458" data-end="515">production of 100% renewable synthetic terpene resins</strong>, which can replace petrochemical derivatives in <strong data-start="564" data-end="601">coatings, varnishes and adhesives</strong>.</p>
<p data-start="604" data-end="1315" data-is-last-node="" data-is-only-node="">In the <strong data-start="611" data-end="628">medical field</strong>, camphene is used as an adjunct in treatments for <strong data-start="679" data-end="730">urolithiasis (the elimination of kidney stones)</strong> <a class="decorated-link" href="https://pmc.ncbi.nlm.nih.gov/articles/PMC3897628/" target="_new" rel="noopener" data-start="731" data-end="793"><strong data-start="732" data-end="741"><span role="math" data-start="734" data-end="739" aria-label="1" data-math-source="1" data-client-katex-layout=""><span class="katex"><span class="katex-html" aria-hidden="true"><span class="base"><span class="mord">1</span></span></span></span></span></strong></a>, while numerous studies have investigated its potential pharmacological applications. These include research into its potential <strong data-start="922" data-end="946">hypolipidemic effect</strong> <a class="decorated-link" href="https://pmc.ncbi.nlm.nih.gov/articles/PMC4718691/" target="_new" rel="noopener" data-start="947" data-end="1009"><strong data-start="948" data-end="957"><span role="math" data-start="950" data-end="955" aria-label="2" data-math-source="2" data-client-katex-layout=""><span class="katex"><span class="katex-html" aria-hidden="true"><span class="base"><span class="mord">2</span></span></span></span></span></strong></a>, <strong data-start="1011" data-end="1041">anti-inflammatory activity</strong> <a class="decorated-link" href="https://pmc.ncbi.nlm.nih.gov/articles/PMC11047447/" target="_new" rel="noopener" data-start="1042" data-end="1105"><strong data-start="1043" data-end="1052"><span role="math" data-start="1045" data-end="1050" aria-label="3" data-math-source="3" data-client-katex-layout=""><span class="katex"><span class="katex-html" aria-hidden="true"><span class="base"><span class="mord">3</span></span></span></span></span></strong></a>, <strong data-start="1107" data-end="1131">antioxidant activity</strong> <a class="decorated-link" href="https://pmc.ncbi.nlm.nih.gov/articles/PMC7179440/" target="_new" rel="noopener" data-start="1132" data-end="1194"><strong data-start="1133" data-end="1142"><span role="math" data-start="1135" data-end="1140" aria-label="4" data-math-source="4" data-client-katex-layout=""><span class="katex"><span class="katex-html" aria-hidden="true"><span class="base"><span class="mord">4</span></span></span></span></span></strong></a> and <strong data-start="1199" data-end="1225">expectorant properties</strong> <a class="decorated-link" href="https://jamanetwork.com/journals/jamaotolaryngology/article-abstract/603203" target="_new" rel="noopener" data-start="1226" data-end="1314"><strong data-start="1227" data-end="1236"><span role="math" data-start="1229" data-end="1234" aria-label="5" data-math-source="5" data-client-katex-layout=""><span class="katex"><span class="katex-html" aria-hidden="true"><span class="base"><span class="mord">5</span></span></span></span></span></strong></a>.</p>
<h2>Why Choose Our Camphene?</h2>
<p class="PDq2pG_selectionAnchorContainer" data-start="0" data-end="166">At <strong data-start="3" data-end="31">DMG</strong>, we guarantee that our camphene is produced through a <strong data-start="86" data-end="124">solvent-free manufacturing process</strong> using turpentine derived from pine resin.</p>
<p data-start="168" data-end="407">From this <strong data-start="178" data-end="209">100% renewable raw material</strong>, we manufacture the <strong data-start="230" data-end="247">levo-camphene</strong> isomer. Thanks to our quality management system, we ensure compliance with our product specifications, including <strong data-start="361" data-end="386">olfactory consistency</strong> from batch to batch.</p>
<p data-start="409" data-end="537">We offer a wide range of grades suitable for applications including <strong data-start="477" data-end="511">perfumery, cosmetics, air care</strong> and <strong data-start="516" data-end="536">food flavourings</strong>.</p>
<p data-start="539" data-end="854">Our camphene also complies with the European <strong data-start="584" data-end="604">REACH Regulation</strong>, ensuring full regulatory traceability and an up-to-date Safety Data Sheet (SDS). We also provide the documentation and <strong data-start="725" data-end="747">IFRA certification</strong> required to ensure efficient and safe formulation for perfumery, cosmetics and personal care applications.</p>
<p data-start="856" data-end="994" data-is-last-node="" data-is-only-node="">Interested in working with our camphene or would you like more information? <a class="decorated-link" href="https://dmg.es/en/contact/" target="_new" rel="noopener" data-start="932" data-end="994" data-is-last-node=""><strong data-start="933" data-end="967">Contact us with no obligation.</strong></a></p>
<p>La entrada <a href="https://dmg.es/en/camphene-properties-history-and-applications/">Camphene: Properties, History and Applications</a> se publicó primero en <a href="https://dmg.es/en/a-world-full-of-fragrances/">DMG</a>.</p>
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		<title>Borneol: Properties, History and Applications</title>
		<link>https://dmg.es/en/borneol-properties-history-and-applications/</link>
		
		<dc:creator><![CDATA[dmg_mugasa]]></dc:creator>
		<pubDate>Mon, 29 Jun 2026 07:11:14 +0000</pubDate>
				<category><![CDATA[Aroma Chemicals]]></category>
		<category><![CDATA[Fragrances]]></category>
		<guid isPermaLink="false">https://dmg.es/?p=10991</guid>

					<description><![CDATA[<p>Borneol (CAS 464-45-9) is a bicyclic terpene naturally found in a wide variety of plants, including rosemary, thyme and ginger. With its intense herbal and balsamic aroma, complemented by fresh, cooling notes, borneol is highly valued in the fragrance, cosmetics and personal care industries. &#160; AROMATIC PROFILE Camphoraceous   Woody   Balsamic   Herbal   Minty   Piney   Earthy    &#160; [&#8230;]</p>
<p>La entrada <a href="https://dmg.es/en/borneol-properties-history-and-applications/">Borneol: Properties, History and Applications</a> se publicó primero en <a href="https://dmg.es/en/a-world-full-of-fragrances/">DMG</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p><strong>Borneol</strong> (CAS 464-45-9) is a bicyclic terpene naturally found in a wide variety of plants, including <a href="https://dmg.es/en/rosemary-essential-oil-history-features-and-benefits/">rosemary,</a> <a href="https://dmg.es/en/thyme-essential-oil-a-100-mediterranean-essence/">thyme</a> and <a href="https://dmg.es/en/ginger-essential-oil-properties-history-and-uses/">ginger</a>.</p>
<figure id="attachment_2370" aria-describedby="caption-attachment-2370" style="width: 247px" class="wp-caption aligncenter"><img loading="lazy" decoding="async" class="wp-image-2370 size-medium" src="https://dmg.es/wp-content/uploads/2020/02/Borneol-Puro-Levo-247x300.png" alt="Estructura química del borneol (C10H18)" width="247" height="300" srcset="https://dmg.es/wp-content/uploads/2020/02/Borneol-Puro-Levo-247x300.png 247w, https://dmg.es/wp-content/uploads/2020/02/Borneol-Puro-Levo.png 439w" sizes="(max-width: 247px) 100vw, 247px" /><figcaption id="caption-attachment-2370" class="wp-caption-text">Chemical structure of borneol (C₁₀H₁₈).</figcaption></figure>
<p>With its <strong>intense herbal and balsamic aroma</strong>, complemented by fresh, cooling notes, borneol is highly valued in the <strong>fragrance, cosmetics and personal care industries</strong>.</p>
<p>&nbsp;</p>
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<th style="border: 1px solid #ddd; padding: 10px; background: #2E7D32; color: #ffffff; text-align: center;">AROMATIC PROFILE</th>
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<td style="border: 1px solid #ddd; padding: 10px; text-align: center;"><strong>Camphoraceous   Woody   Balsamic   Herbal   Minty   Piney   Earthy   </strong></td>
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<p>&nbsp;</p>
<p>At room temperature, borneol appears as an <strong>opaque, white crystalline solid with a slightly cool feel to the touch</strong>. These organoleptic characteristics are reflected in its Chinese name, <em>bingpian</em>, which literally translates as <strong>&#8220;ice (冰, bīng) flakes (片, piàn).&#8221;</strong></p>
<h1>Methods of Obtaining Borneol</h1>
<p class="isSelectedEnd">Historically, borneol was obtained from the naturally crystallized resin found in the fissures of the <em>Dryobalanops aromatica</em> tree.</p>
<p>Although it can still be isolated from essential oils containing naturally occurring borneol, today it is more commonly produced by chemical synthesis. This process typically also yields varying amounts of <strong>isoborneol</strong> (CAS 124-76-5), a stereoisomer of borneol with its own commercial applications, which we will discuss later as it is also one of our manufactured products.</p>
<figure id="attachment_2379" aria-describedby="caption-attachment-2379" style="width: 300px" class="wp-caption aligncenter"><img loading="lazy" decoding="async" class="wp-image-2379 size-medium" src="https://dmg.es/wp-content/uploads/2020/02/Isoborneol-300x269.png" alt="Estructura química del isoborneol" width="300" height="269" srcset="https://dmg.es/wp-content/uploads/2020/02/Isoborneol-300x269.png 300w, https://dmg.es/wp-content/uploads/2020/02/Isoborneol.png 440w" sizes="(max-width: 300px) 100vw, 300px" /><figcaption id="caption-attachment-2379" class="wp-caption-text">Chemical structure of isoborneol</figcaption></figure>
<h1>A Brief History of Borneol</h1>
<p class="isSelectedEnd">Native to the island of Borneo, from which it takes its name, borneol was traditionally used by Malay communities in spiritual and funerary rituals.</p>
<p class="isSelectedEnd">Valued more highly than gold, it became an important commodity in ancient maritime trade. Historical records indicate that it was already being exported to China during the Han Dynasty (206 BC–220 AD).</p>
<p class="isSelectedEnd">Since then, its use has become firmly established, particularly within <strong>Traditional Chinese Medicine (TCM)</strong>, where it has long been employed for conditions affecting the nervous system, respiratory tract and cardiovascular health, among many other applications.</p>
<p>Its significance was such that Li Shizhen devoted a section to borneol in the <em>Bencao Gangmu</em> (1596), one of the most influential encyclopaedic works on Chinese medicine and botany.</p>
<figure id="attachment_10986" aria-describedby="caption-attachment-10986" style="width: 400px" class="wp-caption aligncenter"><img loading="lazy" decoding="async" class="wp-image-10986" src="https://dmg.es/wp-content/uploads/2026/06/Bencao_Gangmu-200x300.jpg" alt="Illustrations from the 1596 edition of the Bencao Gangmu. Public Domain via Wikimedia Commons" width="400" height="600" srcset="https://dmg.es/wp-content/uploads/2026/06/Bencao_Gangmu-200x300.jpg 200w, https://dmg.es/wp-content/uploads/2026/06/Bencao_Gangmu-683x1024.jpg 683w, https://dmg.es/wp-content/uploads/2026/06/Bencao_Gangmu-768x1152.jpg 768w, https://dmg.es/wp-content/uploads/2026/06/Bencao_Gangmu.jpg 960w" sizes="(max-width: 400px) 100vw, 400px" /><figcaption id="caption-attachment-10986" class="wp-caption-text">Illustrations from the 1596 edition of the Bencao Gangmu. Public Domain via Wikimedia Commons</figcaption></figure>
<p>&nbsp;</p>
<p>Its historical medicinal use extends well beyond China and can also be found in traditional medical systems such as <strong>Ayurveda</strong>, originating in the Indian subcontinent.</p>
<h1>Borneol Applications in Modern Industry</h1>
<p class="isSelectedEnd">Today, borneol is an exceptionally versatile ingredient whose distinctive organoleptic profile makes it valuable across a wide range of industries:</p>
<ul data-spread="false">
<li><strong>Food:</strong> Used as a <strong>flavouring agent</strong> in products such as beverages, ice cream and chewing gum.</li>
<li><strong>Cosmetics:</strong> Widely appreciated in skincare products for its <strong>cooling sensation</strong> and pleasant fragrance.</li>
<li><strong>Perfumery:</strong> Frequently incorporated into fragrance compositions to provide <strong>fresh, herbal top notes</strong>.</li>
</ul>
<p>In addition, scientific research continues to support many of the properties traditionally attributed to borneol, including <strong>anti-inflammatory (<a href="https://www.sciencedirect.com/science/article/abs/pii/S1382668920300053">1</a>)</strong>, <strong>analgesic (<a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC12358148/">2</a>)</strong>, <strong>antibacterial</strong> <strong>(</strong><a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC12196741/"><strong>3</strong></a><strong>) </strong>and <strong>neuroprotective(<a href="https://www.nature.com/nature-index/topics/l4/neuroprotective-effects-of-borneol-in-ischemic-stroke-management">4</a>)</strong> effects.</p>
<h1>Why Choose Our Borneol?</h1>
<p class="isSelectedEnd">In the global market for aromatic ingredients, consistency and purity are essential for successful formulations.</p>
<p class="isSelectedEnd">At <strong>Destilerías Muñoz Gálvez</strong>, we are committed to supplying raw materials that meet the highest quality standards while adapting to the technical requirements of each customer and application.</p>
<p class="isSelectedEnd">As part of this commitment, we offer <strong>borneol in a range of grades</strong>, produced by chemical synthesis from pure gum turpentine (CAS 8006-64-2).</p>
<p class="isSelectedEnd">Our extensive expertise in borneol manufacturing has made us <strong>one of Europe&#8217;s leading producers</strong> of this ingredient and the <strong>Lead Registrant for its REACH registration</strong>.</p>
<p>If you are interested in working with our borneol or would like further information, <a href="https://dmg.es/en/contact/"><strong>please do not hesitate to contact us</strong></a>.</p>
<p>La entrada <a href="https://dmg.es/en/borneol-properties-history-and-applications/">Borneol: Properties, History and Applications</a> se publicó primero en <a href="https://dmg.es/en/a-world-full-of-fragrances/">DMG</a>.</p>
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