1-十九烷醇

1-十九烷醇
	IUPAC名; nonadecan-1-ol
別名	1-十九醇; 正十九醇
識別
CAS號	1454-84-8
PubChem	80281
ChemSpider	72522
SMILES	CCCCCCCCCCCCCCCCCCCO;
性質
化學式	C19H40O
摩爾質量	284.52 g·mol−1
熔點	59—61 °C（332—334 K）; 62—63 °C（335—336 K）
沸點	204—217 °C（477—490 K）（3 torr）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

1-十九烷醇是一種有機化合物，化學式為C₁₉H₄₀O，可由十九酸的還原反應製得。^[3]它和溴在三苯基膦催化下反應^[4]，或和四溴化碳、三苯基膦在二氯甲烷中反應^[5]，可以得到1-溴十九烷。它和對甲苯磺酰氯反應，生成相應的酯。^[6]

參考文獻[編輯]

^ ^1.0 ^1.1 James Cason, Helen J. Wolfhagen, Winifred Tarpey, Raylene E. Adams. BRANCHED-CHAIN FATTY ACIDS. X. SYNTHESIS OF ACIDS WITH BRANCHING METHYL GROUPS NEAR THE CARBOXYL. The Journal of Organic Chemistry. 1949-01, 14 (1): 147–154 [2021-03-17]. ISSN 0022-3263. doi:10.1021/jo01153a021 （英語）.
^ Scholl, A. W.; Morrison, J. G. Preparation and properties of n-nonadecyl and n-eicosyl formates. West Va. Univ. Bull., Proc. West Va. Acad. Sci., 1955. V1954. 26: 35-37. CAN50: 44260.
^ Juma'a R. Al Dulayymi, Mark S. Baird, Evan Roberts. The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis. Tetrahedron. 2005-12, 61 (50): 11939–11951 [2021-03-17]. doi:10.1016/j.tet.2005.09.056. （原始內容存檔於2018-07-02）（英語）.
^ Oldřich Kocián, Karel Stránský, Jiří Závada. Unsaturated analogues of 1-triacontanol. Collection of Czechoslovak Chemical Communications. 1982, 47 (5): 1346–1355 [2021-03-17]. ISSN 0010-0765. doi:10.1135/cccc19821346. （原始內容存檔於2018-06-05）（英語）.
^ Yasuhisa Yamamura, Yuri Nakazawa, Shoichi Kutsumizu, Kazuya Saito. Molecular packing in two bicontinuous Ia 3̄ d gyroid phases of calamitic cubic mesogens BABH( n ): roles in structural stability and reentrant behavior. Physical Chemistry Chemical Physics. 2019, 21 (42): 23705–23712 [2021-03-17]. ISSN 1463-9076. doi:10.1039/C9CP04424H （英語）.
^ Kaoru Marukawa, Hirosato Takikawa, Kenji Mori. Synthesis of the Enantiomers of Some Methyl-branched Cuticular Hydrocarbons of the Ant, Diacamma sp.. Bioscience, Biotechnology, and Biochemistry. 2001-01, 65 (2): 305–314 [2021-03-17]. ISSN 0916-8451. doi:10.1271/bbb.65.305. （原始內容存檔於2022-01-21）（英語）.

[Cason-1] 1.0 ^1.1 James Cason, Helen J. Wolfhagen, Winifred Tarpey, Raylene E. Adams. BRANCHED-CHAIN FATTY ACIDS. X. SYNTHESIS OF ACIDS WITH BRANCHING METHYL GROUPS NEAR THE CARBOXYL. The Journal of Organic Chemistry. 1949-01, 14 (1): 147–154 [2021-03-17]. ISSN 0022-3263. doi:10.1021/jo01153a021 （英語）.

[2] Scholl, A. W.; Morrison, J. G. Preparation and properties of n-nonadecyl and n-eicosyl formates. West Va. Univ. Bull., Proc. West Va. Acad. Sci., 1955. V1954. 26: 35-37. CAN50: 44260.

[3] Juma'a R. Al Dulayymi, Mark S. Baird, Evan Roberts. The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis. Tetrahedron. 2005-12, 61 (50): 11939–11951 [2021-03-17]. doi:10.1016/j.tet.2005.09.056. （原始內容存檔於2018-07-02）（英語）.

[4] Oldřich Kocián, Karel Stránský, Jiří Závada. Unsaturated analogues of 1-triacontanol. Collection of Czechoslovak Chemical Communications. 1982, 47 (5): 1346–1355 [2021-03-17]. ISSN 0010-0765. doi:10.1135/cccc19821346. （原始內容存檔於2018-06-05）（英語）.

[5] Yasuhisa Yamamura, Yuri Nakazawa, Shoichi Kutsumizu, Kazuya Saito. Molecular packing in two bicontinuous Ia 3̄ d gyroid phases of calamitic cubic mesogens BABH( n ): roles in structural stability and reentrant behavior. Physical Chemistry Chemical Physics. 2019, 21 (42): 23705–23712 [2021-03-17]. ISSN 1463-9076. doi:10.1039/C9CP04424H （英語）.

[6] Kaoru Marukawa, Hirosato Takikawa, Kenji Mori. Synthesis of the Enantiomers of Some Methyl-branched Cuticular Hydrocarbons of the Ant, Diacamma sp.. Bioscience, Biotechnology, and Biochemistry. 2001-01, 65 (2): 305–314 [2021-03-17]. ISSN 0916-8451. doi:10.1271/bbb.65.305. （原始內容存檔於2022-01-21）（英語）.

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