W288101
亚苄基丙酮
≥98%, FG
别名:
亚苄基丙酮, 甲基苯乙烯基酮, 苄叉丙酮
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关于此项目
线性分子式:
C6H5CH=CHCOCH3
CAS Number:
分子量:
146.19
FEMA编号:
2881
Beilstein:
742047
EC 号:
欧洲委员会编号:
158
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
7.024
NACRES:
NA.21
Agency:
meets purity specifications of JECFA
生物来源
synthetic
等级
FG
Halal
Kosher
Agency
meets purity specifications of JECFA
管理合规性
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 172.515
蒸汽压
0.01 mmHg ( 25 °C)
方案
≥98%
沸点
260-262 °C (lit.)
mp
39-42 °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
anise; cinnamon; jam; balsamic; spicy; floral; sweet
SMILES字符串
[H]\C(=C(\[H])c1ccccc1)C(C)=O
InChI
1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+
InChI key
BWHOZHOGCMHOBV-BQYQJAHWSA-N
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一般描述
Benzylideneacetone is used in the fragrance industry for its sweet pea-like odor. It is one of the major constituents of Monanthotaxis capea essential oil. Studies suggest that apart from skatole and androstenone, benzylideneacetone may also be one of the volatile compounds, which contributes to the development of boar taint in fat samples.
生化/生理作用
5-10ppm 时的味道
其他说明
天然存在：大豆和弗吉尼亚烟草。
警示用语：
Warning
危险声明
危险分类
Skin Irrit. 2 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
253.4 °F - closed cup
闪点(°C)
123 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Phenylbutane Derivatives as Main Constituents of Monanthotaxis capea Essential Oil.
Lamaty G, et al.
J. Essent. Oil Res., 4(1), 33-39 (1992)
Role of 4-phenyl-3-buten-2-one in boar taint: identification of new compounds related to sensorial descriptors in pig fat.
Rius Sole MA & Garcia Regueiro JA.
Journal of Agricultural and Food Chemistry, 49(11), 5303-5309 (2001)
Bin Cao et al.
Organic & biomolecular chemistry, 10(6), 1239-1245 (2011-12-20)
An efficient and easy procedure to synthesize the pyridinyl analogues of dibenzylideneacetone (pyr-dba) was developed by the condensation of substituted nicotinaldehyde and acetone in the presence of K(2)CO(3) in toluene-EtOH-H(2)O solvent system. Structurally diverse pyr-dba, including quinolinyl dba, can be
Jiyong Zhang et al.
The Journal of organic chemistry, 71(7), 2918-2921 (2006-03-25)
The first efficient asymmetric synthesis of obolactone 1 has been accomplished in 11 steps and with a 15% overall yield in which Brown's enantioselective allylation reactions and ring-closing metathesis reaction are key steps.
Ikuro Abe et al.
Organic letters, 4(21), 3623-3626 (2002-10-12)
[reaction: see text] Substrate specificities of plant polyketide synthases (PKSs) were investigated using analogues of malonyl-CoA, the extension unit of the polyketide chain elongation reactions. When incubated with methylmalonyl-CoA and 4-coumaroyl-CoA, plant PKSs (chalcone synthase from Scutellaria baicalensis, stilbene synthase
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