{"id":234,"date":"2023-01-09T16:20:41","date_gmt":"2023-01-09T16:20:41","guid":{"rendered":"https:\/\/graywolfslair.com\/?p=234"},"modified":"2023-03-21T22:21:41","modified_gmt":"2023-03-21T22:21:41","slug":"8-5-oh-sweet-mary-what-is-that-perfume-youre-wearing","status":"publish","type":"post","link":"https:\/\/graywolfslair.com\/index.php\/8-essential-oil-safety\/8-5-oh-sweet-mary-what-is-that-perfume-youre-wearing\/","title":{"rendered":"8.5 Oh Sweet Mary, What is that perfume you&#8217;re wearing?"},"content":{"rendered":"\n<p>When discussing either cannabis flowers or concentrates in detail, the subject of odor comes up, leading to a discussion of the entourage effect of Sweet Mary&#8217;s panoply of engaging smells, noted for their ability to freely penetrates double zip lock baggies and quickly permeate whole rooms or vehicles.<\/p>\n\n\n\n<p>In Sweet Mary II we identified over 400 compounds adding to Sweet Mary&#8217;s entourage, but all odors aren&#8217;t created equal, so which ones are the loudest?<\/p>\n\n\n\n<p>In a paper published by Rice and Koziel on characterizing the impact of the different volatile compounds in marijuana, they identified the dozen loudest from fresh material stuffed in a duffle bag?<\/p>\n\n\n\n<p>Check out the engaging: &nbsp;Characterizing the Smell of Marijuana by Odor Impact of Volatile Compounds, by Rice and Koziel @ PLOS.org. &nbsp;<\/p>\n\n\n\n<p>http:\/\/journals.plos.org\/plosone\/article?id=10.1371\/journal.pone.0144160<\/p>\n\n\n\n<p>The following are the dozen most odiferous cannabis compounds, in order of human odor threshold pungency, as well as their physical properties. &nbsp;Of note, is that the chemical composition is of greater impact than vapor pressure:<\/p>\n\n\n\n<p><strong>1.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Nonanal<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C9 H18 O<\/td><\/tr><tr><td>CAS<\/td><td><a href=\"https:\/\/web.archive.org\/web\/20210919130235\/http:\/\/www.commonchemistry.org\/ChemicalDetail.aspx?ref=124-19-6\">124-19-6<\/a><\/td><\/tr><tr><td>Molar mass<\/td><td>142.24166000<\/td><\/tr><tr><td>Appearance<\/td><td>colorless to pale yellow clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.81900&nbsp;to&nbsp;0.82700&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>-18C\/-0.4F<\/td><\/tr><tr><td>Boiling point<\/td><td>191.00&nbsp;to&nbsp; 193.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>145.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 63.00 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.532000 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>96 mg\/L @ 25 \u00b0C (exp)<\/td><\/tr><tr><td>Odor<\/td><td>waxy aldehydic rose fresh orris orange peel fatty peely<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>2.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Decanol,<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C10 H22 O<\/td><\/tr><tr><td>CAS<\/td><td>112-30-1<\/td><\/tr><tr><td>Molar mass<\/td><td>158.28454000<\/td><\/tr><tr><td>Appearance<\/td><td>colorless clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.82500&nbsp;to&nbsp;0.83100&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>6.90&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Boiling point<\/td><td>231.10&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>180.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 82.00 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.008510 mm\/Hg @ 25.00 \u00b0C.<\/td><\/tr><tr><td>Solubility in water<\/td><td>37 mg\/L @ 25 \u00b0C (exp)<\/td><\/tr><tr><td>Odor<\/td><td>fatty waxy floral orange sweet clean watery<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>3.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; o-Cymene<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C10 H14<\/td><\/tr><tr><td>CAS<\/td><td>527-84-4<\/td><\/tr><tr><td>Molar mass<\/td><td>134.22158000<\/td><\/tr><tr><td>Appearance<\/td><td>colorless to pale yellow clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.877 g\/cm3 at 25 \u00b0C (77 \u00b0F)<\/td><\/tr><tr><td>Melting Point<\/td><td>-71\/-72C\/-96\/-98F<\/td><\/tr><tr><td>Boiling point<\/td><td>177.00&nbsp;to&nbsp; 179.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>123.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 50.60 \u00b0C. ) (est)<\/td><\/tr><tr><td>Vapor pressure<\/td><td>1.500000 mm\/Hg @ 25.00 \u00b0C.<\/td><\/tr><tr><td>Solubility in water<\/td><td>23.3 mg\/L @ 25 \u00b0C (exp)<\/td><\/tr><tr><td>Odor<\/td><td>&nbsp;<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>4.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Isobutyraldehyde<\/strong>, aka 2-methyl-1-propanal<\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C4 H8 O<\/td><\/tr><tr><td>CAS<\/td><td>78-84-2<\/td><\/tr><tr><td>Molar mass<\/td><td>72.10696000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless clear liquid<\/td><\/tr><tr><td>Density<\/td><td>0.78300&nbsp;to&nbsp;0.78800&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>-65.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Boiling point<\/td><td>63.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>-18.89C\/-2F<\/td><\/tr><tr><td>Vapor pressure<\/td><td>173.00 mm\/Hg @ 25.00 \u00b0C.<\/td><\/tr><tr><td>Solubility in water<\/td><td>3.124e+004 mg\/L @ 25 \u00b0C (est)<\/td><\/tr><tr><td>Odor<\/td><td>Fresh aldehydic floral green<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>5.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 1-Chloroacetophenone<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C<sub>6<\/sub>H<sub>5<\/sub>COCH<sub>2<\/sub>Cl<\/td><\/tr><tr><td>CAS<\/td><td>532-27-4<\/td><\/tr><tr><td>Molar mass<\/td><td>154.59 g\/mol<\/td><\/tr><tr><td>Appearance<\/td><td>White crystaline solid<\/td><\/tr><tr><td>Density<\/td><td>1.324 g\/cm<sup>3&nbsp;<\/sup>solid<\/td><\/tr><tr><td>Melting Point<\/td><td>58C\/136.4F<\/td><\/tr><tr><td>Boiling point<\/td><td>247C\/476.6F<\/td><\/tr><tr><td>Flash point<\/td><td>118C\/244F<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.0054 mm Hg at 68\u00b0 F (NTP, 1992)<\/td><\/tr><tr><td>Solubility in water<\/td><td>less than 1 mg\/mL at 66\u00b0 F (NTP, 1992)<\/td><\/tr><tr><td>Odor<\/td><td>Chemical mace, apple blossoms when dilute<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>6.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Nerol&nbsp;<\/strong>aka 2,6-octadien-1-ol, 3,7-dimethyl-(2z)<\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C10 H18 O<\/td><\/tr><tr><td>CAS<\/td><td>106-25-2<\/td><\/tr><tr><td>Molar mass<\/td><td>154.25266000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.87500&nbsp;to&nbsp;0.88300&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>-15C\/5F<\/td><\/tr><tr><td>Boiling point<\/td><td>225.00&nbsp;to&nbsp; 227.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>226.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 107.78 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.013000 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>255.8 mg\/L @ 25 \u00b0C (est)<\/td><\/tr><tr><td>Odor<\/td><td>sweet natural neroli citrus magnolia<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>7.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Propylamine<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C3 H9 N<\/td><\/tr><tr><td>CAS<\/td><td>107-10-8<\/td><\/tr><tr><td>Molar mass<\/td><td>59.11173000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless to yellow clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.71400&nbsp;to&nbsp;0.72000&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>-83C\/-117F<\/td><\/tr><tr><td>Boiling point<\/td><td>47.00&nbsp;to&nbsp; 48.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>-22.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( -30.00 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>328.757996 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>1000000 mg\/L @ 20 \u00b0C (exp)<\/td><\/tr><tr><td>Odor<\/td><td>Ammoniacal<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>8.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; o-Guaiacol<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C7 H8 O2<\/td><\/tr><tr><td>CAS<\/td><td>90-05-1<\/td><\/tr><tr><td>Molar mass<\/td><td>124.13916000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless to pale yellow clear oily liquid to solid (est)<\/td><\/tr><tr><td>Density<\/td><td>1.12300&nbsp;to&nbsp;1.13000&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>28.00&nbsp;to&nbsp; 32.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Boiling point<\/td><td>205.00&nbsp;to&nbsp; 206.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>180.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 82.22 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.179000 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>7226 mg\/L @ 25 \u00b0C (est)<\/td><\/tr><tr><td>Odor<\/td><td>Phenolic smoke spice vanilla woody<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>9.0&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Linalyl acetate&nbsp;<\/strong>aka 1,6-octadien-3-ol, 3,7-dimethyl-, acetate<\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C12 H20 O2<\/td><\/tr><tr><td>CAS<\/td><td>115-95-7<\/td><\/tr><tr><td>Molar mass<\/td><td>196.28980000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>0.90300&nbsp;to&nbsp;0.91200&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>85 \u00b0C (185 \u00b0F; 358 K)<\/td><\/tr><tr><td>Boiling point<\/td><td>220.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>185.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 85.00 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.116000 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>20.12 mg\/L @ 25 \u00b0C (est)<\/td><\/tr><tr><td>Odor<\/td><td>Sweet green citrus bergamot lavender woody<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>10.0&nbsp;&nbsp;&nbsp;&nbsp; Methyl anthranilate<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C8 H9 N O2<\/td><\/tr><tr><td>CAS<\/td><td>134-30-3<\/td><\/tr><tr><td>Molar mass<\/td><td>151.16513000<\/td><\/tr><tr><td>Appearance<\/td><td>Pale yellow to dark yellow clear liquid to solid (est)<\/td><\/tr><tr><td>Density<\/td><td>1.16100&nbsp;to&nbsp;1.16900&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>23.00&nbsp;to&nbsp; 24.50&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Boiling point<\/td><td>238.00&nbsp;to&nbsp; 241.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>220.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 104.44 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>0.016000 mm\/Hg @ 25.00 \u00b0C. (est)<\/td><\/tr><tr><td>Solubility in water<\/td><td>2,850 mg\/liter @ 25 deg C<\/td><\/tr><tr><td>Odor<\/td><td>Fruity grape orange flower neroli<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>11.0&nbsp;&nbsp;&nbsp;&nbsp; Benzaldehyde<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C7 H6 O<\/td><\/tr><tr><td>CAS<\/td><td>100-52-7<\/td><\/tr><tr><td>Molar mass<\/td><td>106.12402000<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless to pale yellow clear liquid (est)<\/td><\/tr><tr><td>Density<\/td><td>1.04100&nbsp;to&nbsp;1.04600&nbsp;@&nbsp; 25.00 \u00b0C.<\/td><\/tr><tr><td>Melting Point<\/td><td>-26.00&nbsp;to&nbsp; -25.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Boiling point<\/td><td>178.00&nbsp;to&nbsp; 179.00&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>145.00&nbsp;\u00b0F.&nbsp;TCC&nbsp;( 62.78 \u00b0C. )<\/td><\/tr><tr><td>Vapor pressure<\/td><td>1.270000 mm\/Hg @ 25.00 \u00b0C.<\/td><\/tr><tr><td>Solubility in water<\/td><td>0.3 g\/100 mL (20 \u00b0C)<\/td><\/tr><tr><td>Odor<\/td><td>strong sharp sweet bitter almond cherry<\/td><\/tr><tr><td>&nbsp;<\/td><td>&nbsp;<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>12.0&nbsp;&nbsp;&nbsp;&nbsp; Limonene<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>1.1&nbsp; Physical Properties<\/strong><\/td><\/tr><tr><td>Chemical formula<\/td><td>C10H16<\/td><\/tr><tr><td>CAS<\/td><td>5989-27-5<\/td><\/tr><tr><td>Molar mass<\/td><td>136.23 g\/mole<\/td><\/tr><tr><td>Appearance<\/td><td>Colorless to pale yellow<\/td><\/tr><tr><td>Density<\/td><td>0.84<\/td><\/tr><tr><td>Melting Point<\/td><td>-40\u00b0C (-40\u00b0F)<\/td><\/tr><tr><td>Boiling point<\/td><td>176.00\/178&nbsp;\u00b0C. @ 760.00&nbsp;mm Hg<\/td><\/tr><tr><td>Flash point<\/td><td>43.33 \u00b0C\/110.00&nbsp;\u00b0F<\/td><\/tr><tr><td>Vapor pressure<\/td><td>1.550000 mm\/Hg @ 25.00 \u00b0C.<\/td><\/tr><tr><td>Solubility in water<\/td><td>4.581 mg\/L @ 25 \u00b0C (est)<\/td><\/tr><tr><td>Odor<\/td><td>Citrus herbal terpene camphor<\/td><\/tr><\/tbody><\/table><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>When discussing either cannabis flowers or concentrates in detail, the subject of odor comes up, leading to a discussion of the entourage effect of Sweet [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[43],"tags":[],"class_list":["post-234","post","type-post","status-publish","format-standard","hentry","category-8-essential-oil-safety"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>8.5 Oh Sweet Mary, What is that perfume you&#039;re wearing? 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What it discovered\u2026","rel":"","context":"In &quot;8. Essential Oil Safety&quot;","block_context":{"text":"8. Essential Oil Safety","link":"https:\/\/graywolfslair.com\/index.php\/category\/8-essential-oil-safety\/"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/graywolfslair.com\/wp-content\/uploads\/2023\/04\/Figure-1.png?resize=350%2C200&ssl=1","width":350,"height":200},"classes":[]},{"id":225,"url":"https:\/\/graywolfslair.com\/index.php\/8-essential-oil-safety\/8-1-sweet-marys-charms\/","url_meta":{"origin":234,"position":1},"title":"8.1 Sweet Mary&#8217;s Charms","author":"GrayWolf","date":"January 9, 2023","format":false,"excerpt":"\u00a0Sweet Mary's Charms by JD Ellis and Rob Brown\u00a0 Wowza!\u00a0 Because of the rapidly growing popularity for vaporizing cannabis concentrates, as well adding additional terpenes to concentrates and carts, I started out to write an article on the properties of the volatile compounds in our beloved sweet Mary, highlighting any\u2026","rel":"","context":"In &quot;8. Essential Oil Safety&quot;","block_context":{"text":"8. Essential Oil Safety","link":"https:\/\/graywolfslair.com\/index.php\/category\/8-essential-oil-safety\/"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":463,"url":"https:\/\/graywolfslair.com\/index.php\/10-the-alchemist-resource\/10-7-crc\/10-7-5-multicomponent-adsorption-of-volatile-organic-compounds-in-the-liquid-phase-predictive-engineering-models-molecular-simulations-and-experiments\/","url_meta":{"origin":234,"position":2},"title":"10.7.5 Multicomponent Adsorption of Volatile Organic Compounds in the Liquid Phase: Predictive, Engineering Models, Molecular Simulations and Experiments.","author":"GrayWolf","date":"January 10, 2023","format":false,"excerpt":"Check out this study and paper done by C Brunch and published 2015 in Chemistry: https:\/\/pdfs.semanticscholar.org\/b29b\/a8094c8edd6d2dc58c33a983b55a77d8e626.pdf","rel":"","context":"In &quot;10.7 CRC&quot;","block_context":{"text":"10.7 CRC","link":"https:\/\/graywolfslair.com\/index.php\/category\/10-the-alchemist-resource\/10-7-crc\/"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":246,"url":"https:\/\/graywolfslair.com\/index.php\/8-essential-oil-safety\/8-11-dr-justin-fischedick-on-plant-terpenes\/","url_meta":{"origin":234,"position":3},"title":"8.11 Dr Justin Fischedick On Plant Terpenes","author":"GrayWolf","date":"January 9, 2023","format":false,"excerpt":"Perhaps the best opening question to start the article on sweet Mary\u2019s charms, would be why are we so interested in these volatile compounds.\u00a0 Our own interest started prior to November of 2013, because by that time we sponsored Dr. Justin Fischedick as a guest lecturer in Portland.\u00a0 He lectured\u2026","rel":"","context":"In &quot;8. 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Rasdan titled \"The Total Synthesis of Cannabinoids\".\u00a0 Published by the Department of Chemistry, Carlton University\u2019s \u201cTotal Synthesis of Natural Products.\u00a0 Available\u2026","rel":"","context":"In &quot;10. The Alchemist Resource&quot;","block_context":{"text":"10. The Alchemist Resource","link":"https:\/\/graywolfslair.com\/index.php\/category\/10-the-alchemist-resource\/"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":572,"url":"https:\/\/graywolfslair.com\/index.php\/15-diy-equipment\/15-26-acoustical-extraction\/","url_meta":{"origin":234,"position":5},"title":"15.26 Acoustical Extraction","author":"GrayWolf","date":"January 11, 2023","format":false,"excerpt":"Besides the highly individualized hand jive style of extraction using a screen, the question arises as to how much support we might expect from music, or other acoustical dry sieving techniques. 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