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线性分子式:
C6H5CH=CHCO2CH(CH3)2
化学文摘社编号:
分子量:
190.24
FEMA Number:
2939
Council of Europe no.:
325
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.732
EC Number:
231-949-0
NACRES:
NA.21
MDL number:
Organoleptic:
balsam; fruity
Grade:
FG
Halal
Kosher
Halal
Kosher
Biological source:
synthetic
Food allergen:
no known allergens
产品名称
肉桂酸异丙酯, ≥96%, FG
SMILES string
CC(C)OC(=O)\C=C\c1ccccc1
InChI
1S/C12H14O2/c1-10(2)14-12(13)9-8-11-6-4-3-5-7-11/h3-10H,1-2H3/b9-8+
InChI key
RGACABDFLVLVCT-CMDGGOBGSA-N
biological source
synthetic
grade
FG
Halal
Kosher
reg. compliance
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 172.515
assay
≥96%
refractive index
n20/D 1.546 (lit.)
bp
273 °C (lit.)
density
1.02 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
balsam; fruity
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Application
Isopropyl cinnamate can be used as a perfuming agent in cosmetics and as a flavoring ingredient in food industries.
General description
Isopropyl cinnamate can be used as a flavoring and fragrance ingredient. It is one of the key constituents of the essential oil of Fortunella crassifolia peel.
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
此项目有
Chemical composition and antimicrobial activity of the essential oil of Kumquat (Fortunella crassifolia Swingle) Peel.
Wang YW, et al.
International Journal of Molecular Sciences, 13(3), 3382-3393 (2012)
Comparison of estimated daily intakes of flavouring substances with no-observed-effect levels
Munro IC and Danielewska-Nikiel B
Food And Chemical Toxicology, 44(6), 758-809 (2006)
Cinnamic acid derivatives in cosmetics: current use and future prospects
Gunia-Krzyzak A, et al.
International Journal of Cosmetic Science, 40(4), 356-366 (2018)
Inhibition of Anopheles gambiae odorant receptor function by mosquito repellents.
Tsitoura P, et al.
The Journal of Biological Chemistry, 290(12), 7961-7972 (2015)
Structure?activity relationships of phenylpropanoids as antifeedants for the pine weevil Hylobius abietis.
Bohman B, et al.
Journal of Chemical Ecology, 34(3), 339-352 (2007)
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