Investigating Indoor Chemistry of Terpinolene Through the Use of a New Derivatization Agent
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2015/07/19
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Description:The gas-phase ozonolysis of terpinolene was investigated using a new carbonyl derivatization agent: O-tert-butylhydroxylamine hydrochloride (TBOX). Reaction products from the terpinolene/O3 system were collected in a water-filled impinger, TBOX was added, and the mixture was heated to 70 degrees C for two hours followed by extraction with 0.5 mL toluene. Using this lower molecular weight derivatization agent resulted in the observation of a tricarbonyl reaction product: 3,6-dioxoheptanal. Additionally, three other carbonyl compounds were observed: Methyl glyoxal, 4-methylcyclohex-3-en-1-one, and 6-oxo-3-(propan-2- ylidene)heptanal. The mechanism(s) for formation of these compounds is most likely due to O3 addition to terpinolene's carbon-carbon double bonds while the tricarbonyl formation may be due to a reaction from secondary OH radicals. Understanding the formation of di- and tricarbonyl species as a result of terpene ozonolysis is an important element of indoor occupant exposure assessment. [Description provided by NIOSH]
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Pages in Document:171-173
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NIOSHTIC Number:nn:20052758
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Citation:Healthy Buildings 2015 America: Innovation in a Time of Energy Uncertainty and Climate Adaptation, HB 2015, July 19-22, 2015, Boulder, Colorado. Santa Cruz, CA: International Society of Indoor Air Quality and Climate, 2015 Jul; 1:171-173
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Email:ozw0@cdc.gov
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Federal Fiscal Year:2015
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Peer Reviewed:False
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Source Full Name:Healthy Buildings 2015 America: Innovation in a Time of Energy Uncertainty and Climate Adaptation, HB 2015, July 19-22, 2015, Boulder, Colorado
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Main Document Checksum:urn:sha-512:00aa0bbb24fb813075a165d464cf2bd4c6bba616a6c673a3179d0b2a77cc51f788c82100a21cabba35ec1d4bf618b0e9d58af2da523e5897d604d3c228eb073b
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