檸檬烯二環氧化物

檸檬烯二環氧化物
英文名	limonene diepoxide
別名	檸檬烯二氧化物
識別
CAS號	96-08-2
PubChem	232703
ChemSpider	202849
SMILES	CC12CCC(CC1O2)C3(CO3)C;
InChI	InChI=1S/C10H16O2/c1-9-4-3-7(5-8(9)12-9)10(2)6-11-10/h7-8H,3-6H2,1-2H3;
InChIKey	RBHIUNHSNSQJNG-UHFFFAOYSA-N
性質
化學式	C10H16O2
摩爾質量	168.23 g·mol−1
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

檸檬烯二環氧化物（英語：Limonene diepoxide），又稱檸檬烯二氧化物（英語：Limonene dioxide）^[1]，是一種有機化合物，化學式C₁₀H₁₆O₂，可見於日本柳杉^[2]、煙草^[3]、薑^[4]等物種。工業上常用易得的檸檬烯原料氧化得到^[1]，如將檸檬烯利用氧化鋁和過氧化氫作為催化劑進行氧化，可得到具有立體選擇性的檸檬烯二環氧化物^[5]，也可用過氧乙酸進行逐一氧化，先氧化環戊烯結構得到檸檬烯單環氧化物，後氧化異丙烯基支鏈得到^[6]。檸檬烯二環氧化物可用於生產交聯劑、粘結劑以及環氧樹脂等聚合物材料^[1]。

參考資料

^ ^1.0 ^1.1 ^1.2 Luc Charbonneau, Xavier Foster, Dongyuan Zhao, Serge Kaliaguine. Catalyst-Free Epoxidation of Limonene to Limonene Dioxide. ACS Sustainable Chemistry & Engineering. 2018, 6 (4): 5115–5. doi:10.1021/acssuschemeng.7b04782.
^ Gaston Vernin; Jacques Metzger; Jean-Pierre Mondon; Jean-Claude Pieribattesti. GC/MS Analysis of the Leaf Oil of Cryptomeria japonica D. Don from Reunion Island. Journal of Essential Oil Research. 2012-04, 3 (4). doi:10.1080/10412905.1991.9697930.
^ Xianzhong Zhang; Hongjian Gao; Lifen Zhang; Donghong Liu; Xingqian Ye. Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition. Industrial Crops and Products. 2012-03, 39. doi:10.1016/J.INDCROP.2012.02.029.
^ Fan Gong; Ying-Sing Fung; Yi-Zeng Liang. Determination of volatile components in ginger using gas chromatography-mass spectrometry with resolution improved by data processing techniques. Journal of Agricultural and Food Chemistry. 2004-10, 52 (21). doi:10.1021/JF040102Z （英語）.
^ Anderson J. Bonon, Juliana O. Bahú, Bruno C. Klein, Dalmo Mandelli, Rubens Maciel Filho. Green production of limonene diepoxide for potential biomedical applications. Catalysis Today. 2022,. 388-389: 288-300. doi:10.1016/j.cattod.2020.06.030.
^ James V. Crivello, Bo Yang. Studies of synthesis and cationic photopolymerization of three isomeric monoterpene diepoxides. Journal of Polymer Science Part A: Polymer Chemistry. 1995, 33 (11): 1881-1890. doi:10.1002/pola.1995.080331116.

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[:0-1] 1.0 ^1.1 ^1.2 Luc Charbonneau, Xavier Foster, Dongyuan Zhao, Serge Kaliaguine. Catalyst-Free Epoxidation of Limonene to Limonene Dioxide. ACS Sustainable Chemistry & Engineering. 2018, 6 (4): 5115–5. doi:10.1021/acssuschemeng.7b04782.

[2] Gaston Vernin; Jacques Metzger; Jean-Pierre Mondon; Jean-Claude Pieribattesti. GC/MS Analysis of the Leaf Oil of Cryptomeria japonica D. Don from Reunion Island. Journal of Essential Oil Research. 2012-04, 3 (4). doi:10.1080/10412905.1991.9697930.

[3] Xianzhong Zhang; Hongjian Gao; Lifen Zhang; Donghong Liu; Xingqian Ye. Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition. Industrial Crops and Products. 2012-03, 39. doi:10.1016/J.INDCROP.2012.02.029.

[4] Fan Gong; Ying-Sing Fung; Yi-Zeng Liang. Determination of volatile components in ginger using gas chromatography-mass spectrometry with resolution improved by data processing techniques. Journal of Agricultural and Food Chemistry. 2004-10, 52 (21). doi:10.1021/JF040102Z （英語）.

[5] Anderson J. Bonon, Juliana O. Bahú, Bruno C. Klein, Dalmo Mandelli, Rubens Maciel Filho. Green production of limonene diepoxide for potential biomedical applications. Catalysis Today. 2022,. 388-389: 288-300. doi:10.1016/j.cattod.2020.06.030.

[6] James V. Crivello, Bo Yang. Studies of synthesis and cationic photopolymerization of three isomeric monoterpene diepoxides. Journal of Polymer Science Part A: Polymer Chemistry. 1995, 33 (11): 1881-1890. doi:10.1002/pola.1995.080331116.

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