Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

166170

Sigma-Aldrich

Cinnamyl acetate

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)
Linear Formula:
CH3CO2CH2CH=CHC6H5
CAS Number:
103-54-8
Molecular Weight:
176.21
EC Number:
203-121-9
MDL number:
MFCD00008722
UNSPSC Code:
12352100
PubChem Substance ID:
24850157
NACRES:
NA.22

Quality Level

100

Assay

99%

form

powder

refractive index

n20/D 1.541 (lit.)

bp

265 °C (lit.)

solubility

alcohol: soluble(lit.)
glycerol: insoluble(lit.)
water: insoluble(lit.)

density

1.057 g/mL at 25 °C

SMILES string

CC(=O)OC\C=C\c1ccccc1

InChI

1S/C11H12O2/c1-10(12)13-9-5-8-11-6-3-2-4-7-11/h2-8H,9H2,1H3/b8-5+

InChI key

WJSDHUCWMSHDCR-VMPITWQZSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Cinnamyl acetate is a fragrance ingredient. Palladium catalyzed allylic alkylation of cinnamyl acetate using sodium diethyl 2-methylmalonate and novel ferrocenyl Schiff base has been investigated.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

WGK

WGK 1

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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

S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45 Suppl 1, S53-S57 (2007-11-23)
A toxicologic and dermatologic review of cinnamyl acetate when used as a fragrance ingredient is presented.
Schiff bases containing ferrocenyl and thienyl units and their utility in the palladium catalyzed allylic alkylation of cinnamyl acetate.
Pou D, et al
Journal of Organometallic Chemistry, 692(22), 5017-5025 (2007)
Ji-Eun Lee et al.
Pesticide biochemistry and physiology, 168, 104644-104644 (2020-07-28)
To find new and safe type of control agents against phytopathogenic fungi, the fumigant antifungal activity of 10 plant essential oils and constituents identified in cinnamon bark (Cinnamomum verum) and lemongrass (Cymbopogon citratus) essential oils was investigated against two phytopathogenic
Emilie Deletre et al.
Parasites & vectors, 8, 316-316 (2015-06-13)
Laboratory and field studies showed that repellent, irritant and toxic actions of common public health insecticides reduce human-vector contact and thereby interrupt disease transmission. One of the more effective strategies to reduce disease risk involves the use of long-lasting treated

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