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Merck
CN

W261602

Lauryl acetate

≥98%, FG

Synonym(s):

Dodecyl acetate, Lauryl acetate

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About This Item

Linear Formula:
CH3CO2(CH2)11CH3
CAS Number:
Molecular Weight:
228.37
FEMA Number:
2616
Council of Europe no.:
200
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.010
EC Number:
203-995-1
NACRES:
NA.21
MDL number:
Organoleptic:
fresh; waxy; sweet
Grade:
FG
Halal
Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
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Product Name

Lauryl acetate, ≥98%, FG

SMILES string

CCCCCCCCCCCCOC(C)=O

InChI

1S/C14H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-16-14(2)15/h3-13H2,1-2H3

InChI key

VZWGRQBCURJOMT-UHFFFAOYSA-N

biological source

synthetic

grade

FG
Halal
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

assay

≥98%

refractive index

n20/D 1.432 (lit.)

bp

150 °C/15 mmHg (lit.)

density

0.865 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

fresh; waxy; sweet

Quality Level

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hcodes

Hazard Classifications

Aquatic Chronic 4

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

Regulatory Information

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Ido Yosha et al.
Journal of agricultural and food chemistry, 56(17), 8045-8049 (2008-08-12)
Alginate-gelatin beads with dispersed droplets of a model pheromone, dodecyl acetate, were prepared as a vehicle for slow release of pheromones into the atmosphere over a prolonged period of time. The beads are prepared in two steps, the first being
K D Philipson et al.
The American journal of physiology, 248(1 Pt 2), H147-H150 (1985-01-01)
We have used charged amphiphiles as phospholipid analogues to modulate the interaction of Ca2+ with myocardial sarcolemma. The amphiphiles were dodecyl sulfate, dodecyltrimethylamine, and lauryl acetate; these are anionic, cationic, and neutral molecules, respectively. The hydrophobic alkyl chain is identical
S V B Janardhan Garikipati et al.
Applied and environmental microbiology, 75(20), 6545-6552 (2009-08-25)
Whole-cell biocatalysis to oxidize naphthalene to 1-naphthol in liquid-liquid biphasic systems was performed. Escherichia coli expressing TOM-Green, a variant of toluene ortho-monooxygenase (TOM), was used for this oxidation. Three different solvents, dodecane, dioctyl phthalate, and lauryl acetate, were screened for
B O Zimma et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 189(10), 769-775 (2003-09-05)
The bumblebee Bombus (Psithyrus) norvegicus Sp.-Schn. is an obligate social parasite of B. (Pyrobombus) hypnorum L. Behavioural observations indicated that nest-invading B. norvegicus females may use allomones to defend themselves against attacking host workers. However, so far no defensive chemicals
Stephen J Martin et al.
Journal of chemical ecology, 36(8), 855-863 (2010-05-29)
Semiochemicals influence many aspects of insect behavior, including interactions between parasites and their hosts. We studied the chemical recognition system of bumblebees (Bombus) by examining the cuticular hydrocarbon cues of 14 species, including five species of social parasites, known as

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