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Merck
CN

36103

Acetyleugenol

reference material, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Synonym(s):

Eugenyl acetate, 4-Allyl-2-methoxyphenyl acetate, O-Acetyleugenol, Eugenol acetate

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About This Item

Empirical Formula (Hill Notation):
C12H14O3
CAS Number:
Molecular Weight:
206.24
EC Number:
202-235-6
UNSPSC Code:
41116107
MDL number:
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InChI key

SCCDQYPEOIRVGX-UHFFFAOYSA-N

InChI

1S/C12H14O3/c1-4-5-10-6-7-11(15-9(2)13)12(8-10)14-3/h4,6-8H,1,5H2,2-3H3

SMILES string

COc1cc(CC=C)ccc1OC(C)=O

grade

reference material

assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

refractive index

n20/D 1.518 (lit.)

bp

281-286 °C (lit.)

density

1.079 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

shipped in

wet ice

storage temp.

−20°C

Quality Level

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General description

This reference material (RM) is produced and certified in accordance with ISO/IEC 17025. This RM is traceable to primary material from an NMI, e.g. NIST or NMIJ.

Acetyleugenol is a phytochemical compound belonging to the class of alkylbenzenes, a group of volatile plant toxins. It is widely found in consumed spices, aromatic herbs, and other plants including anise, basil, cinnamon, fennel, nutmeg, clove Syzygium aromaticum (L.) essential oil, pimento, rose, ylang-ylang, etc.

Application

Acetyleugenol may be used as a reference material in pepper and its other varieties, Longhu Rendan pills and clove extract using chromatography techniques.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1B

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

287.6 °F - closed cup

flash_point_c

142 °C - closed cup


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A new strategy based on gas chromatography--high resolution mass spectrometry (GC--HRMS-Q-Orbitrap) for the determination of alkenylbenzenes in pepper
Rivera-Perez A, et al.
Food Chemistry, 126727-126727 (2020)
J Chromatogr B Analyt Technol Biomed Life Sci
Wang, et al.
Analytical Methods : Advancing Methods and Applications, 6(11), 3713-3719 (2014)
Gas chromatographic determination of eugenol in ethanol extract of cloves
Myint S, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 679(1-2), 193-195 (1996)
Acetyleugenol from Acacia nilotica (L.) exhibits a strong antibacterial activity and its phenyl and indole analogs show a promising anti-TB potential
Abdulhamid A, et al.
Microbiological research, 12, 1-15 (2020)

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