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![[3-(乙氧羰基)丙基]三苯基溴化膦 97%](/deepweb/assets/sigmaaldrich/product/structures/101/490/c9797f74-da99-4610-8812-8572dc35c41d/640/c9797f74-da99-4610-8812-8572dc35c41d.png)
生物来源
synthetic
质量水平
等级
FG
Fragrance grade
Halal
Kosher
Agency
follows IFRA guidelines
管理合规性
EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515
方案
≥95%
包含
α-tocopherol,synthetic as stabilizer
citric acid, synthetic as stabilizer
折射率
n20/D 1.523 (lit.)
沸点
97-98 °C/12 mmHg (lit.)
密度
1.019 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
green; citrus; floral; peach
SMILES字符串
[H]C(=O)CCc1ccccc1
InChI
1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H,4,7H2
InChI key
YGCZTXZTJXYWCO-UHFFFAOYSA-N
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一般描述
氢肉桂醛是肉桂精油的挥发性成分之一。
生化/生理作用
20ppm 时的味道
其他说明
天然存在：肉桂、番茄、鸡肉、啤酒和牛至。
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
203.0 °F - closed cup
闪点(°C)
95 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
A comparison of essential oil constituents of bark, leaf, root and fruit of cinnamon (Cinnamomum zeylanicum Blum) grown in Sri Lanka.
Paranagama PA, et al.
Journal of the National Science Foundation of Sri Lanka, 29(3-4) (2010)
Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils.
Senanayake UM, et al.
Journal of Agricultural and Food Chemistry, 26(4), 822-824 (1978)
Extraction of essential oils from five cinnamon leaves and identification of their volatile compound compositions.
Wang R, et al.
Innovative Food Science & Emerging Technologies, 10(2), 289-292 (2009)
Shih-Shen Chou Lin et al.
Phytotherapy research : PTR, 25(10), 1511-1518 (2011-03-12)
The purpose of this study was to analyse the major compound in the leaf essential oil of Cinnamomum osmophloeum Kaneh. and to examine its in vivo toxicity and cytokine-modulatory effects. The HS-GC/MS and quantitative HPLC analyses showed the concentrations of
Samir BouzBouz et al.
Organic letters, 5(11), 1995-1997 (2003-05-24)
[reaction: see text] The synthesis of (+)-strictifolione was achieved from 3-phenylproprionaldehyde by using enantioselective allyltitanations to control the stereogenic centers at C6, C4', and C6' and a cross-methathesis to control the configuration of the double bond at C1'-C2'.
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