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W244104

Sigma-Aldrich

Ethyl laurate

≥98%, FCC, FG

Synonym(s):

Ethyl dodecanoate, Ethyl laurate, Lauric acid ethyl ester

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About This Item

Linear Formula:
CH3(CH2)10COOC2H5
CAS Number:
106-33-2
Molecular Weight:
228.37
FEMA Number:
2441
Beilstein:
1769671
EC Number:
203-386-0
Council of Europe no.:
375
MDL number:
MFCD00015065
UNSPSC Code:
12164502
PubChem Substance ID:
24901086
Flavis number:
9.099
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 172.515

Assay

≥98%

refractive index

n20/D 1.432 (lit.)

bp

269 °C (lit.)

density

0.86 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

waxy; floral; soapy; sweet

SMILES string

CCCCCCCCCCCC(=O)OCC

InChI

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

InChI key

MMXKVMNBHPAILY-UHFFFAOYSA-N

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Application


  • RIFM fragrance ingredient safety assessment, ethyl laurate, CAS Registry Number 106-33-2.: This study, published in Food and Chemical Toxicology, assesses the safety of ethyl laurate as a fragrance ingredient. The comprehensive review includes various toxicological endpoints and supports the safe use of ethyl laurate in fragrance formulations (Api et al., 2022).

  • Application of a statistically enhanced, novel, organic solvent stable lipase from Bacillus safensis DVL-43.: This research explores the use of a novel lipase from Bacillus safensis in biocatalysis, highlighting its stability in organic solvents and its potential applications in the synthesis of ethyl laurate and other esters. The findings indicate significant improvements in enzymatic efficiency and potential industrial applications (Kumar et al., 2014).

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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D R Bevan et al.
Cancer letters, 57(2), 173-179 (1991-05-01)
Effects of vehicles and of asbestos on disposition of benzo[a]pyrene (B[a]P) were examined in vivo. [3H]B[a]P dissolved in triethylene glycol, ethyl laurate, or tricaprylin was intratracheally administered to male Sprague-Dawley rats. Excretion was most rapid when triethylene glycol was the
Lianli Li et al.
International journal of pharmaceutics, 237(1-2), 77-85 (2002-04-17)
An ethyl laurate-based microemulsion system with Tween 80 as surfactant, propylene glycol and ethanol as cosolvents was developed for intranasal delivery of diazepam. Phase behavior and solubilization capacity of the microemulsion system were characterized and in vivo nasal absorption of
A Botsi et al.
Carbohydrate research, 241, 37-46 (1993-03-17)
The inclusion complexes of cyclomaltoheptaose (beta CD) and heptakis(2,3,6-tri-O-methyl)cyclomaltoheptaose (TM-beta CD) with the four major components of the pheromone of the olive fruit fly (Dacus oleae), namely 1,7-dioxaspiro[5.5]undecane, (-)-alpha-pinene, nonanal, and ethyl dodecanoate, and the complex of heptakis(2,6-di-O-methyl)cyclomaltoheptaose (DM-beta CD)
Hydrocracking of ethyl laurate on bifunctional micro-/mesoporous zeolite catalysts.
Oliver Busse et al.
ChemSusChem, 3(5), 563-565 (2010-05-04)
Jun-min Zhang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 33(2), 215-218 (2010-06-26)
To study the chemical constituents from pine needles of Cedrus deodara. Chemical constituents were isolated by silica gel and Sephadex LH-20 column chromatography. The structures of the isolated compounds were elucidated through spectroscopic analysis. The compounds were identified as 9-hydroxy-dodecanoic
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