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Squalane | CAS:111-01-3
Squalane
  • 名称:角鲨烷; 异三十烷; 2,6,10,15,19,23-六甲基二十四烷 | Squalane
  • CAS号:111-01-3
  • 别名:2,6,10,15,19,23-Hexamethyltetracosane
  • 分子式:C30H62
  • 分子量:422.81
  • EINESC号:203-825-6

产品描述

物理化学性质

熔点 -38 ºC
沸点 176 ºC (0.05 mmHg)
闪点 218 ºC
密度 0.8085
折射率 1.451-1.4525

安全数据

危险品标志 Xi
危险类别码 R36/37/38
安全说明书 S26;S36

SDS

来源 SDS样本
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Studies of the formation of all-carbon quaternary centres, en route to lyngbyatoxin A. A comparison of phenyl and 7-substituted indole systems.Janne E Tønder et al.Organic & biomolecular chemistry, 2(10), 1447-1455 (2004-05-12) Rhodococcus opacus strain PD630 as a new source of high-value single-cell oil? Isolation and characterization of triacylglycerols and other storage lipids.M Wältermann et al.Microbiology (Reading, England), 146 ( Pt 5), 1143-1149 (2000-06-01) Preparation of ethyl magnesium bromide for regiospecific analysis of triacylglycerols.Yasuhiro Ando et al.Journal of oleo science, 57(8), 459-462 (2008-07-16) Replacement of the lactone moiety on podophyllotoxin and steganacin analogues with a 1, 5-disubstituted 1, 2, 3-triazole via ruthenium-catalyzed click chemistry.Imperio D Bioorganic & Medicinal Chemistry, 15(21), 6748-6757 (2007) An improved synthesis of (+)-3, 4-O-isopropylidene butyne.Jiang B Synthetic Communications, 25(22), 3641-3645 (1995) (-)-N-[(11)C]propyl-norapomorphine: a positron-labeled dopamine agonist for PET imaging of D(2) receptors.D R Hwang et al.Nuclear medicine and biology, 27(6), 533-539 (2000-11-01) New reagent system for attaining high regio- and stereoselectivities in allylic displacement of 4-cyclopentene-1,3-diol monoacetate with aryl- and alkenylmagnesium bromides.Yuichi Kobayashi et al.Organic letters, 7(2), 183-186 (2005-01-14) Trifluoromethanesulfonic anhydride-promoted alpha-bromination of ketones with grignard reagent or magnesium bromide.T Nishiyama et al.Chemical & pharmaceutical bulletin, 48(12), 1999-2002 (2001-01-06) A direct method for regiospecific analysis of TAG using alpha-MAG.F Turon et al.Lipids, 37(8), 817-821 (2002-10-10) A new efficient synthetic method for 2- and 4-hydroxy-17 alpha-ethynylestradiol.R G Xie et al.Steroids, 55(11), 488-490 (1990-11-01)
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