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Key Documents

Safety Information

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:
Molecular Weight:
228.37
FEMA Number:
2616
EC Number:
Council of Europe no.:
200
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.010
NACRES:
NA.21

biological source

synthetic

Quality Level

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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Hazard Statements

Precautionary Statements

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 Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

W261602-SAMPLE-K:
W261602-4KG:
W261602-1KG:
W261602-VAR-K:
W261602-300G:
W261602-1KG-K:4548173971032
W261602-BULK-K:
W261602-9KG-K:
W261602-4KG-K:4548173971049
W261602-9KG:
W261602-SAMPLE:


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Kenneth M MacDonald et al.
Journal of chemical ecology, 29(10), 2385-2389 (2003-12-20)
Larvae of the western flower thrips Frankliniella occidentalis are known to produce an anal droplet containing decyl acetate (10Ac) and dodecyl acetate (12Ac), which act as an alarm pheromone. Analysis by GC showed that the combined mass of 10Ac and
Daniël Groen et al.
Biochimica et biophysica acta, 1838(1 Pt B), 310-318 (2013-10-16)
This paper describes two synthetic lipid models designed to replace human stratum corneum (SC) in studies of the impact of volatile organic chemicals on the molecular organization of the skin barrier lipids. The models built upon previously developed self-assembled lipid
A M Beedle et al.
Biophysical journal, 79(1), 260-270 (2000-06-27)
We have recently identified farnesol, an intermediate in the mevalonate pathway, as a potent endogenous modulator and blocker of N-type calcium channels (Roullet, J. B., R. L. Spaetgens, T. Burlingame, and G. W. Zamponi. 1999. J. Biol. Chem. 274:25439-25446). Here
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
Brent L Waguespack et al.
Journal of chromatography. A, 1078(1-2), 171-180 (2005-07-13)
A variety of porous polymer monoliths (PPMs) have been synthesized using the 'conduct-as-cast' format. The resulting polymers have been evaluated for use as separation media in capillary electrochromatography (CEC). The results have shown that substituting a small percentage of the

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