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Cinnamyl isobutyrate

analytical standard

Synonym(s):

Isobutyric acid cinnamyl ester

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About This Item

Linear Formula:
(CH3)2CHCO2CH2CH=CHC6H5
CAS Number:
Molecular Weight:
204.26
EC Number:
MDL number:
UNSPSC Code:
12164502
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥96.0% (GC)

shelf life

limited shelf life, expiry date on the label

refractive index

n20/D 1.523-1.528
n20/D 1.524 (lit.)

bp

254 °C (lit.)

density

1.008 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

SMILES string

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

InChI

1S/C13H16O2/c1-11(2)13(14)15-10-6-9-12-7-4-3-5-8-12/h3-9,11H,10H2,1-2H3/b9-6+

InChI key

KLKQSZIWHVEARN-RMKNXTFCSA-N

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General description

Cinnamyl isobutyrate (CIB) is an aroma component, naturally occurring in the essential oil of cinnamon bark. This fragrance ingredient is widely found in fragrances used in shampoos, decorative cosmetics, fine fragrances, toilet soaps and other toiletries, non-cosmetic products including household cleaners, detergents, etc.

Application

Cinnamyl isobutyrate may be used as an analytical reference standard for the quantification of the analyte in watermelon (EG) flavored hookah tobacco and leaf oil of Heteropyxis dehniae Suess. using gas chromatography coupled to mass spectrometry (GC-MS).

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Cinnamyl isobutyrate decreases plasma glucose levels and total energy intake from a standardized breakfast: A randomized, crossover intervention
Hochkogler MC, et al.
Molecular Nutrition And Food Research, 62(17), 1701038-1701038 (2018)
Fragrance material review on cinnamyl isobutyrate
Bhatia PS, et al.
Food And Chemical Toxicology, 45(1), S74-S77 (2007)
Composition and bioactivity of the leaf essential oil of Heteropyxis dehniae from Zimbabwe
Sibanda S, et al.
Journal of Ethnopharmacology, 92(1), 107-111 (2004)
Specific features of human monocytes activation by monophosphoryl lipid A
Chentouh R, et al.
Scientific reports, 8(1), 1-13 (2018)

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