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Merck
CN

W261602

Sigma-Aldrich

Lauryl acetate

≥98%, FG

Synonym(s):

Dodecyl acetate, Lauryl acetate

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About This Item

Linear Formula:
CH3CO2(CH2)11CH3
CAS Number:
112-66-3
Molecular Weight:
228.37
FEMA Number:
2616
EC Number:
203-995-1
Council of Europe no.:
200
MDL number:
MFCD00008973
UNSPSC Code:
12164502
PubChem Substance ID:
24901208
Flavis number:
9.010
NACRES:
NA.21
Organoleptic:
fresh; waxy; sweet
Grade:
FG
Halal
Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens

Key Documents

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biological source

synthetic

Quality Level

400

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

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

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Related Categories

Hazard Statements

H413

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 4

Storage Class Code

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBT2562
SHBT0914
SHBS3727
SHBQ3572
SHBP9954

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Developing new anti-cancer drugs.
Ricardo de Souza Pereira
Recent patents on anti-cancer drug discovery, 6(1), 1-5 (2010-11-30)
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
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
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
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
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