1-十六炔

1-十六炔
英文名	1-hexadecyne
识别
CAS号	629-74-3
PubChem	12396
SMILES	C#CCCCCCCCCCCCCCC;
InChI	InChI=1S/C16H30/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h1H,4-16H2,2H3;
InChIKey	UCIDYSLOTJMRAM-UHFFFAOYSA-N
性质
化学式	C16H30
摩尔质量	222.41 g·mol−1
熔点	+15.0
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

1-十六炔是一种有机化合物，化学式C₁₆H₃₀，可见于北美金缕梅^[1]、鱼腥草^[2]、羽叶金合欢^[3]、辽东栎（Quercus liaotungensis）^[4]、牛樟^[5]等物种。其可在吸附有氢原子的单晶硅（111）晶面上自发吸附形成一层致密的单分子层^[6]^[7]。

参考资料

^ Engel R; Gutmann M; Hartisch C; Kolodziej H; Nahrstedt A. Study on the composition of the volatile fraction of Hamamelis virginiana. Planta Medica. 1998-04, 64 (3). doi:10.1055/S-2006-957420.
^ Minmin Liang; Meiling Qi; Changbin Zhang; Shan Zhou; Ruonong Fu; Junxiong Huang. Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation. Analytica Chimica Acta. 2005-02, 531 (1). doi:10.1016/J.ACA.2004.09.082.
^ 李贵军，汪帆. 臭菜挥发油化学成分的GC-MS分析. 中国调味品. 2014, (6): 118-120. doi:10.3969/j.issn.1000-9973.2014.06.031.
^ 周敬林，王斌赫，王国宝. 2种柞树叶片和树皮中的挥发性化学成分鉴定. 蚕业科学. 2017, 43 (3): 459-466. doi:10.13441/j.cnki.cykx.2017.03.015.
^ Cheng, Sen-Sung, Chun-Ya Lin, Chih-Kai Yang, Ying-Ju Chen, Min-Jay Chung, ,Shang-Tzen Chan. Chemical Polymorphism and Composition of Leaf Essential Oils of Cinnamomum kanehirae Using Gas Chromatography/Mass Spectrometry, Cluster Analysis, and Principal Component Analysis. Journal of Wood Chemistry and Technology. 2015, 35 (3): 207-219. doi:10.1080/02773813.2014.924967.
^ Luc ScheresMarcel GiesbersHan Zuilhof. Self-Assembly of Organic Monolayers onto Hydrogen-Terminated Silicon: 1-Alkynes Are Better Than 1-Alkenes. Langmuir. 2010, 26 (13): 10924–10929. doi:10.1021/la100858q.
^ Bart Rijksen，Sidharam P. Pujari，Luc Scheres，; et al. Hexadecadienyl Monolayers on Hydrogen-Terminated Si(111): Faster Monolayer Formation and Improved Surface Coverage Using the Enyne Moiety. Langmuir. 2012, 28 (16): 6577–6588. doi:10.1021/la204770r.

这是一篇关于有机化合物的小作品。您可以通过编辑或修订扩充其内容。

[1] Engel R; Gutmann M; Hartisch C; Kolodziej H; Nahrstedt A. Study on the composition of the volatile fraction of Hamamelis virginiana. Planta Medica. 1998-04, 64 (3). doi:10.1055/S-2006-957420.

[2] Minmin Liang; Meiling Qi; Changbin Zhang; Shan Zhou; Ruonong Fu; Junxiong Huang. Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation. Analytica Chimica Acta. 2005-02, 531 (1). doi:10.1016/J.ACA.2004.09.082.

[3] 李贵军，汪帆. 臭菜挥发油化学成分的GC-MS分析. 中国调味品. 2014, (6): 118-120. doi:10.3969/j.issn.1000-9973.2014.06.031.

[4] 周敬林，王斌赫，王国宝. 2种柞树叶片和树皮中的挥发性化学成分鉴定. 蚕业科学. 2017, 43 (3): 459-466. doi:10.13441/j.cnki.cykx.2017.03.015.

[5] Cheng, Sen-Sung, Chun-Ya Lin, Chih-Kai Yang, Ying-Ju Chen, Min-Jay Chung, ,Shang-Tzen Chan. Chemical Polymorphism and Composition of Leaf Essential Oils of Cinnamomum kanehirae Using Gas Chromatography/Mass Spectrometry, Cluster Analysis, and Principal Component Analysis. Journal of Wood Chemistry and Technology. 2015, 35 (3): 207-219. doi:10.1080/02773813.2014.924967.

[6] Luc ScheresMarcel GiesbersHan Zuilhof. Self-Assembly of Organic Monolayers onto Hydrogen-Terminated Silicon: 1-Alkynes Are Better Than 1-Alkenes. Langmuir. 2010, 26 (13): 10924–10929. doi:10.1021/la100858q.

[7] Bart Rijksen，Sidharam P. Pujari，Luc Scheres，; et al. Hexadecadienyl Monolayers on Hydrogen-Terminated Si(111): Faster Monolayer Formation and Improved Surface Coverage Using the Enyne Moiety. Langmuir. 2012, 28 (16): 6577–6588. doi:10.1021/la204770r.

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