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234591

Sigma-Aldrich

Methyl laurate

99.5%

Synonym(s):

Lauric acid methyl ester, Methyl dodecanoate

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About This Item

Linear Formula:
CH3(CH2)10CO2CH3
CAS Number:
111-82-0
Molecular Weight:
214.34
Beilstein:
1767780
EC Number:
203-911-3
MDL number:
MFCD00008966
UNSPSC Code:
12352100
PubChem Substance ID:
24854049
NACRES:
NA.22

Assay

99.5%

form

liquid

refractive index

n20/D 1.431 (lit.)

bp

262 °C/766 mmHg (lit.)

mp

4-5 °C (lit.)

solubility

water: insoluble 0.00759 g/L at 25 °C (practically)

density

0.87 g/mL at 25 °C (lit.)

food allergen

no known allergens

SMILES string

CCCCCCCCCCCC(=O)OC

InChI

1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3

InChI key

UQDUPQYQJKYHQI-UHFFFAOYSA-N

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General description

Hydrogenation of methyl laurate catalyzed by diatomite supported Pd-M (M=Cu, Co, Ni) bimetal nanocatalysts has been reported. IR absorption spectrum of methyl laurate in carbon tetrachloride and carbon disulphide solutions has been compared with the spectra of derivatives deuterated in the ω-methyl group and α-methylene groups.

Application

Methyl laurate has been used in selective synthesis of the secondary amide surfactant, N-methyl lauroylethanolamide.

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

282.2 °F - closed cup

Flash Point(C)

139 °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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Christian Lipok et al.
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A closed atmospheric pressure chemical ionization (APCI) ion source as interface between a gas chromatograph (GC) and a triple quadrupole mass spectrometer (QqQ-MS) was developed. The influence of different ion source conditions, such as humidity, make-up gas flow, and the
The infrared absorption spectra of deuterated esters: III. Methyl laurate.
Jones RN.
Canadian Journal of Chemistry, 40(2), 301-320 (1962)
Néstor M Carballeira et al.
Lipids, 40(10), 1063-1068 (2005-12-31)
The hitherto unknown 2-methylsulfanyldecanoic acid and 2-methylsulfanyldodecanoic acid were synthesized from methyl decanoate and methyl dodecanoate, respectively, through the reaction of lithium diisopropylamide and dimethyldisulfide in THF followed by saponification with potassium hydroxide in ethanol. Both alpha-methylsulfanylated FA were cytotoxic
Jana Olšovská et al.
Journal of the science of food and agriculture, 99(4), 1772-1779 (2018-09-19)
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E Barboza-Silva et al.
Oral microbiology and immunology, 24(4), 265-271 (2009-07-04)
The arginine deiminase system (ADS) of oral bacteria is a major generator of alkali (ammonia) in dental plaque and is considered to have anticaries effects. However, many of the antimicrobial agents used in oral care products may reduce alkali production
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