Sources of fine organic aerosol. 4. Particulate abrasion products from leaf surfaces of urban plants was written by Rogge, Wolfgang F.;Hildemann, Lynn M.;Mazurek, Monica A.;Cass, Glen R.;Simoneit, Bernd R. T.. And the article was included in Environmental Science and Technology in 1993.Recommanded Product: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate This article mentions the following:
Green and dead leaves from 62 plant species characteristic of the Los Angeles area were harvested and composited according to the actual leaf mass distribution for that area. To simulate leaf surface abrasion by the wind, the leaf composites were agitated in clean Teflon bags while a purified air stream flowed through. Fine particles (≤2 μm) shed from the leaf surfaces were extracted and analyzed using gas chromatog./mass spectrometry. Organic constituents including n-alkanes, n-alkanoic and n-alkenoic acids, n-alkanols, n-alkanals, terpenoid compounds, and trace amounts of PAH were identified and quantified. N-Alkanes showed similar concentrations in both dead and green leaf surface matter; mono-, sesqui-, and triterpenoids were depleted in dead leaf material while n-alkanoic acids were enriched in dead leaf abrasion products. It is shown that the higher mol. weight n-alkanes (C27-C33), with their pronounced odd/even C number predominance, provide a suitable marker compound assemblage for tracing vegetative detritus in the urban atm. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Recommanded Product: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate).
rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts