二甲基巰基丙酸

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二甲基巰基丙酸
IUPAC名
(Dimethylsulfaniumyl)propanoate
別名 dimethyl-β-propiothetin
識別
CAS號 7314-30-9  checkY
PubChem 23736
ChemSpider 22195
SMILES
 
  • C[S+](C)CCC(=O)[O-]
InChI
 
  • 1/C5H10O2S/c1-8(2)4-3-5(6)7/h3-4H2,1-2H3
InChIKey DFPOZTRSOAQFIK-UHFFFAOYAW
性質
化學式 C5H10O2S
摩爾質量 134.1967 g·mol⁻¹
外觀 white crystalline powder with hygroscopicity and characteristic odor.[1]
熔點 120 - 125 °C[1]
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

二甲基巰基丙酸(英語:Dimethylsulfoniopropionate,縮寫DMSP)是一種化學式為(CH3)2S+CH2CH2COO有機化合物,常以內鹽形式存在於海洋浮游植物海藻以及某些陸生及水生維管植物中。

生物合成[編輯]

降解[編輯]

參考文獻[編輯]

  1. ^ 1.0 1.1 存档副本. [2013-02-05]. (原始內容存檔於2013-03-06). 
  2. ^ DeBose, Jennifer L.; Sean C. Lema; Gabrielle A. Nevitt. Dimethylsulfoniopropionate as a foraging cue for reef fishes (abstract). Science. 2008-03-07, 319 (5868): 1356 [2008-03-21]. PMID 18323445. doi:10.1126/science.1151109. (原始內容存檔於2008-12-02). Vila-Costa, Maria; Rafel Simo; Hyakubun Harada; Josep M. Gasol; Doris Slezak; Ronald P. Kiene. Dimethylsulfoniopropionate uptake by marine phytoplankton (abstract). Science. 2006-10-27, 314 (5799): 652–654 [2008-03-21]. PMID 17068265. doi:10.1126/science.1131043. (原始內容存檔於2009-12-11). 
  3. ^ Challenger, Frederick; Margaret Isabel Simpson. Studies on biological methylation. Part XII. A precursor of the dimethyl sulphide evolved by Polysiphonia fastigiata. Dimethyl-2-carboxyethylsulphonium hydroxide and its salts. (pdf). Journal of the Chemical Society (London). 2014-07-14, 1948: 1591–1597 [2014-07-14]. PMID 18101461. doi:10.1039/JR9480001591. (原始內容存檔於2018-10-03). 
  4. ^ Scott D. McNeil, Michael L. Nuccio, and Andrew D. Hanson "Betaines and Related Osmoprotectants. Targets for Metabolic Engineering of Stress Resistance" Plant Physiology, August 1999, Vol. 120, pp. 945–949. doi:10.1104/pp.120.4.945

外部連結[編輯]