所有图片(1)
About This Item
线性分子式:
C6H5(CH2)3OH
CAS号:
分子量:
136.19
FEMA编号:
2885
Beilstein:
1857542
EC 号:
欧洲委员会编号:
80
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
2.031
NACRES:
NA.21
性状检查:
balsam; cinnamon; hyacinth; floral; spicy
生物来源:
synthetic
Agency:
meets purity specifications of JECFA
食品过敏原:
no known allergens
推荐产品
生物来源
synthetic
质量水平
Agency
meets purity specifications of JECFA
管理合规性
FCC
FDA 21 CFR 172.515
方案
≥98%
折射率
n20/D 1.526 (lit.)
沸点
119-121 °C/12 mmHg (lit.)
mp
−18 °C (lit.)
密度
1.001 g/mL at 20 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
balsam; cinnamon; hyacinth; floral; spicy
SMILES字符串
OCCCc1ccccc1
InChI
1S/C9H12O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2
InChI key
VAJVDSVGBWFCLW-UHFFFAOYSA-N
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一般描述
3-苯基-1-丙醇是一种挥发性化合物，据报告它存在于苏铁胶 、番石榴果 和蜂蜡中。
应用
化妆品中的防腐剂-这种酒精是一种天然香料，具有抗菌细菌和霉菌的特性。本品可与胡椒醛或胡椒醛联合使用，作为化妆品的防腐剂。
这种醇或其酯衍生物因具有香脂味而可用作鲜花组合物（像丁香花、风信子和百合）的芳香成分。
免责声明
用于研发&或非欧盟(EU)食品用途。不用于零售。
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
248.0 °F - closed cup
闪点(°C)
120 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Paniandy JC, et al.
J. Essent. Oil Res., 12(2), 153-158 (2000)
The aroma of beeswax.
Ferber CE & Nursten HE
Journal of the Science of Food and Agriculture, 28(6), 511-518 (1977)
Chemical composition of the essential oils from Turkish and Honduras Styrax.
Fernandez X, et al.
Flavour and Fragrance Journal, 20(1), 70-73 (2005)
D Belsito et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49 Suppl 2, S256-S267 (2011-08-09)
The cinnamyl phenylpropyl fragrance ingredients are a diverse group of chemical structures that have similar metabolic and toxicity profiles. A toxicological and dermatological review of these fragrance ingredients is presented. The common characteristic structural element of cinnamyl phenylpropyl materials is
Soyeong Kang et al.
The Journal of organic chemistry, 75(1), 237-240 (2009-12-05)
A highly efficient, enantioselective sequence has been developed for the synthesis of (S)- and (R)-dapoxetine. The pathways involve the intermediacy of the 6-membered-ring sulfamate esters 4, which were generated by Du Bois asymmetric C-H amination reactions of the prochiral sulfamate
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