beta-pinen ne demek?

<table> <caption>id="6" |β-Pinen</caption> <tbody> <tr class="odd"> <td></td> </tr> <tr class="even"> <td><table> <tbody> <tr class="odd"> <td></td> <td></td> </tr> </tbody> </table></td> </tr> <tr class="odd"> <td><p>Adlar</p></td> </tr> <tr class="even"> <td><p><a href="Chemical_nomenclature" title="wikilink">IUPAC adları</a></p> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;"> <p>6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptane</p> <p>Pin-2(10)-ene</p> </div></td> </tr> <tr class="odd"> <td><p>Diğer Adlar</p> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;"> <p>6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane</p> <p>2(10)-Pinene</p> <p>Nopinene</p> <p>Pseudopinene</p> </div></td> </tr> <tr class="even"> <td><p>Tanımlayıcılar</p></td> </tr> <tr class="odd"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p><a href="CAS_Registry_Number" title="wikilink">CAS sayısı</a></p> </div></td> </tr> <tr class="even"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p>3D model (<a href="JSmol" title="wikilink">JSmol</a>)</p> </div></td> </tr> <tr class="odd"> <td><p><a href="ChEBI" title="wikilink">ChEBI</a></p></td> </tr> <tr class="even"> <td><p><a href="ChEMBL" title="wikilink">ChEMBL</a></p></td> </tr> <tr class="odd"> <td><p><a href="ChemSpider" title="wikilink">ChemSpider</a></p></td> </tr> <tr class="even"> <td><p><a href="ECHA_InfoCard" title="wikilink"><span title="echa.europa.eu">ECHA Bilgi Kartı</span></a></p></td> </tr> <tr class="odd"> <td><p><a href="KEGG" title="wikilink">KEGG</a></p></td> </tr> <tr class="even"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p><a href="PubChem" title="wikilink">PubChem</a> <abbr title="<nowiki&gt;Compound ID</nowiki&gt;">CID</abbr></p> </div></td> </tr> <tr class="odd"> <td><p><a href="Unique_Ingredient_Identifier" title="wikilink">UNII</a></p></td> </tr> <tr class="even"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p><a href="CompTox_Chemicals_Dashboard" title="wikilink">CompTox Dashboard</a> <span style="font-weight:normal">(<abbr title="<nowiki&gt;U.S. Environmental Protection Agency</nowiki&gt;">EPA</abbr>)</span></p> </div></td> </tr> <tr class="odd"> <td><div class="mw-collapsible mw-collapsed" style="text-align: center; font-size: 95%;"> <div style="line-height: 1.6em; font-weight: bold; font-size: 100%; text-align: left; text-align:left; font-weight:normal; background:transparent;"> <div> <p><a href="International_Chemical_Identifier" title="wikilink">InChI</a></p> </div> </div> <ul> <li><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"> <div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;"> <p>InChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3<sup> <span style="display:none">Y</span></sup></p> </div> <div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;"> <p>Key: WTARULDDTDQWMU-UHFFFAOYSA-N<sup> <span style="display:none">Y</span></sup></p> </div> </div></li> <li><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"> <div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;"> <p>InChI=1/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3</p> </div> <div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;"> <p>Key: WTARULDDTDQWMU-UHFFFAOYAW</p> </div> </div></li> </ul> </div></td> </tr> <tr class="even"> <td><div class="mw-collapsible mw-collapsed" style="text-align: center; font-size: 95%;"> <div style="line-height: 1.6em; font-weight: bold; font-size: 100%; text-align: left; text-align:left; font-weight:normal; background:transparent;"> <div> <p><a href="Simplified_molecular-input_line-entry_system" title="wikilink">SMILES</a></p> </div> </div> <ul> <li><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.6em; word-wrap:break-word; text-indent:-1.5em; text-align:left; font-size:97%; line-height:120%;"> <p>C1(=C)C2CC(CC1)C2(C)C</p> </div></li> </ul> </div></td> </tr> <tr class="odd"> <td><p>Özellikler</p></td> </tr> <tr class="even"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p><a href="Kimyasal_formül" title="wikilink">Kimyasal Formül</a></p> </div></td> </tr> <tr class="odd"> <td><p><a href="Molar_kütle" title="wikilink">Molar kütle</a></p></td> </tr> <tr class="even"> <td><p>Görünüş</p></td> </tr> <tr class="odd"> <td><p><a href="Yoğunluk" title="wikilink">Yoğunluk</a></p></td> </tr> <tr class="even"> <td><p><a href="Kaynama_noktası" title="wikilink">Kaynama noktası</a></p></td> </tr> <tr class="odd"> <td><p><a href="Kaynama_noktası" title="wikilink">Kaynama noktası</a></p></td> </tr> <tr class="even"> <td><p>Termokimya</p></td> </tr> <tr class="odd"> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p><a href="Standard_enthalpy_change_of_combustion" title="wikilink">Std enthalpy of combustion</a> <span style="font-family:sans-serif;font-size:112%;color:black;background-color:transparent;;">(Δ<sub>c</sub><em>H</em><sup>⦵</sup><sub>298</sub>)</span></p> </div></td> </tr> <tr class="even"> <td><p>Tehlikeler</p></td> </tr> <tr class="odd"> <td><p><a href="Parlama_noktası" title="wikilink">Parlama noktası</a></p></td> </tr> <tr class="even"> <td><div style="margin:0 auto; text-align:left;"> <div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"> <p>Sıcaklık ve basınç bilgileri özellikle not edilmiş durumlar dışındaki bilgiler maddenin <a href="standart_koşullar" title="wikilink">standart koşullar</a> altındaki hâline göre verilmiştir (25 °C [77 °F], 100 kPa).</p> </div> </div></td> </tr> <tr class="odd"> <td><p><span style="display:none">Y</span> <span class="reflink plainlinks nourlexpansion">[//en.wikipedia.org/w/index.php?title=Special:ComparePages&amp;rev1=443421864&amp;page2=Beta-Pinene doğrulama]</span> (bu ne <sup><span style="display:none">Y</span><span style="display:none">N</span></sup> ?)</p></td> </tr> <tr class="even"> <td><p>Bilgi kutusu<a href="Vikipedi:Kimyasal_bilgi_tabloları" title="wikilink"> referanslar</a></p></td> </tr> <tr class="odd"> <td></td> </tr> </tbody> </table>

id="6" |β-Pinen

<div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">

Chemical compound

</div>

Beta-Pinen (β- pinen), bitkilerde bulunan organik bir monoterpendir. Pinenin iki izomerinden biridir, Pinenin diğer izomeri ise α-pinen'dir. beta-Pinen, renksiz birsıvıdır. Alkolde çözünebilir ancak suda çözünmez. Odunsu-yeşil çam benzeri bir kokusu vardır. Beta-pinen orman ağaçları tarafından en çok miktarda salınan bileşiklerden biridir.1 Eğer havada oksitlenirse, pinokarveol ve myrtenol ailesinin alilik ürünleri yerine geçer.2

Bulunduğu Bitkiler

Birçok botanik aileye mensup birçok bitkinin yapısında bu bileşik vardır, örneğin:

Kaynakça

Orijinal kaynak: beta-pinen. Creative Commons Atıf-BenzerPaylaşım Lisansı ile paylaşılmıştır.

Footnotes

  1. Geron, C., et al. (2000).

Kategoriler