等级
technical
方案
≥90% (GC)
折射率
n20/D 1.481
密度
0.88 g/mL at 20 °C (lit.)
SMILES字符串
C\C(C)=C\CCC(C)=CCCC(C)=CCCC(C)=O
InChI
1S/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3
InChI key
LTUMRKDLVGQMJU-UHFFFAOYSA-N
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Eyeshields, Gloves
法规信息
新产品
此项目有
Do N Dai et al.
Natural product communications, 9(9), 1359-1360 (2015-04-29)
Fresh leaves of Actephila excelsa (Dazl.) Muell. from Vietnam were steam distilled to produce an oil in a yield of 0.15% (v/w). The essential oil was analyzed by a combination of capillary gas chromatography-flame ionization detection (GC-FID) and gas chromatography
Anuraag Muralidharan et al.
Life sciences, 208, 149-160 (2018-07-23)
Pervasiveness of Alzheimer's disease (AD) across the globe is on rise, devitalizing the essential brain functions of the afflicted individual. Multiple neurological pathways viz., cholinergic, amyloidogenic and tau protein pathways underlying the disease and interdependence make it more complex to
Geonseek Ryu et al.
Archives of pharmacal research, 26(10), 796-799 (2003-11-12)
Two known farnesylacetone derivatives (1 and 2) were isolated from the Korean brown alga Sargassum sagamianum off Jeju Island, Korea. Compounds 1 and 2 were identified as (5E,10Z)-6,10,14-trimethylpentadeca-5,10-dien-2,12-dione and (5E,9E,13E)-6,10,4-trimethyl-pentadeca-5,9,13-trien-2,12-dione, respectively, by comparison with the literature data. Compounds 1 and
Substrate specificity of undecaprenyl pyrophophate synthetase from Lactobacillus plantarum.
Baba T and Allen Jr CA.
Biochemistry, 17(26), 5598-5604 (1978)
Woon-Seob Shin et al.
Vascular pharmacology, 58(4), 299-306 (2013-02-19)
A specific blocker of L-type Ca(2+) channels may be useful in decreasing arterial tone by reducing the open-state probability of L-type Ca(2+) channels. The aim of the present study was to evaluate the farnesylacetones, which are major active constituents of
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