推荐产品
生物来源
synthetic
质量水平
等级
FG
Fragrance grade
Halal
Kosher
Agency
follows IFRA guidelines
meets purity specifications of JECFA
管理合规性
EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
方案
≥99%
沸点
95-96 °C/12 mmHg (lit.)
mp
61-64 °C (lit.)
密度
0.969 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
致敏芳香化合物
no known allergens
性状检查
brown; spicy
SMILES字符串
C\C=C(/C)C(O)=O
InChI
1S/C5H8O2/c1-3-4(2)5(6)7/h3H,1-2H3,(H,6,7)/b4-3+
InChI key
UIERETOOQGIECD-ONEGZZNKSA-N
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应用
- 具有反式-2-甲基-2-丁烯酸功能的高摩尔消光系数联吡啶均相Ru(II)配合物:染料敏化太阳能电池的潜在染料:这项研究探讨了将反式-2-甲基-2-丁烯酸掺入Ru(II)配合物作为染料敏化太阳能电池染料的合成和应用。高摩尔消光系数和良好的光物理特性使该化合物成为增强太阳能电池效率的有希望的候选者(Adeloye等人,2012年)。
- 具有反式-2-甲基-2-丁烯酸功能的混合联吡啶-菲咯啉配体Ru(II)杂配配合物的合成、光物理和电化学性质:这项研究重点研究了具有反式-2-甲基-2-丁烯酸功能的Ru(II)杂配配合物的合成和表征。该研究突出了化合物的物理和电化学性质,证明了其在光电器件和催化应用中的潜力(Adeloye,2011年)。
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
203.0 °F
闪点(°C)
95 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Tigliane-type diterpene esters from Synadenium grantii.
Planta medica, 54(6), 506-510 (1988-12-01)
International journal of immunopharmacology, 18(12), 761-769 (1996-12-01)
The present study was undertaken to assess the influence of 25 organic acids, which appear in high concentrations in tissues of patients with various organic acidaemias, on the proliferation of human peripheral lymphocytes stimulated with concanavalin A (Con A) (a
Applied microbiology and biotechnology, 65(4), 373-376 (2004-07-13)
Candida antarctica lipase fraction B (CAL-B) showed substrate specificity in the synthesis of esters in hexane involving reactions of short-chain acids having linear (acetic and butyric acids) and branched chain (isovaleric acid) structures, an unsaturated (tiglic acid) fatty acid, and
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 26(12), 835-837 (2003-06-05)
To study the chemical constituents of Ligularia vellerea. The compounds were isolated by column chromatography, and the structures were identified by NMR spectral data and other methods. Seven compounds were isolated and identified as 4-hydroxyacetophenone, 8 alpha-hydroxy-7(11)-eremophilen-12, 8 beta-olide, umbelliferone
[Effects of a skin stimulating salve].
Wiener medizinische Wochenschrift (1946), 100(45-46), 758-759 (1950-11-25)
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