Skip to Content
Merck
All Photos(1)

Documents

W293903

Sigma-Aldrich

Isopropyl cinnamate

≥96%, FG

Synonym(s):

Isopropyl 3-phenylpropenoate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5CH=CHCO2CH(CH3)2
CAS Number:
Molecular Weight:
190.24
FEMA Number:
2939
EC Number:
Council of Europe no.:
325
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.732
NACRES:
NA.21

biological source

synthetic

Quality Level

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

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

Looking for similar products? Visit Product Comparison Guide

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.

Application

Isopropyl cinnamate can be used as a perfuming agent in cosmetics and as a flavoring ingredient in food industries.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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)
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)
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)
Inhibition of Anopheles gambiae odorant receptor function by mosquito repellents.
Tsitoura P, et al.
The Journal of Biological Chemistry, 290(12), 7961-7972 (2015)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service