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METHYL LAURATE

Methyl Laurate

CAS: 111-82-0

Molecular Formula: C13H26O2

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METHYL LAURATE - Names and Identifiers

Name Methyl Laurate
Synonyms uniphata40
Methyl Laurate
METHYL LAURATE
METHYL-DODECANATE
Methyl dodecanoate
METHYL DODECANOATE
RARECHEM AL BF 0157
LAURIC ACID METHYL ESTER
DODECANOIC ACID METHYL ESTER
CAS 111-82-0
EINECS 203-911-3
InChI InChI=1/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3
InChIKey UQDUPQYQJKYHQI-UHFFFAOYSA-N

METHYL LAURATE - Physico-chemical Properties

Molecular FormulaC13H26O2
Molar Mass214.34
Density0.87 g/mL at 25 °C (lit.)
Melting Point4-5 °C (lit.)
Boling Point262 °C/766 mmHg (lit.)
Flash Point>230°F
JECFA Number180
Water SolubilityNot miscible in water. Soluble in alcohol, dipropylene glycol.
Solubility It is miscible with ethanol, ether, acetone, benzene, soluble in methanol, chloroform and carbon tetrachloride, insoluble in water.
Vapor Presure0.55Pa at 25℃
AppearanceTransparent liquid
ColorClear colorless to slightly yellow
BRN1767780
Storage Conditionroom temp
Refractive Indexn20/D 1.432
MDLMFCD00008966
Physical and Chemical PropertiesA colorless oily liquid with properties similar to those of alcoholic and floral aromas.
melting point 5.2 ℃
boiling point 262 ℃(102.1kPa)
relative density 0.8702
refractive index 1.4319
solubility, acetone and benzene are miscible.
UseUsed as gas chromatography stationary liquid, food additive and organic synthesis reagent

METHYL LAURATE - Risk and Safety

Hazard SymbolsN - Dangerous for the environment
Dangerous for the environment
Risk Codes50 - Very Toxic to aquatic organisms
Safety DescriptionS24/25 - Avoid contact with skin and eyes.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
UN IDsUN 3082 9 / PGIII
WGK Germany1
RTECSOF0670000
TSCAYes
HS Code2915 90 30
ToxicityLD50 orally in Rabbit: > 2000 mg/kg

METHYL LAURATE - Reference

Reference
Show more
1. Liu Kaiping, Cheng Shengyong, Yu Linna, et al. Preparation and quality evaluation of spider scented valerian triester self-microemulsion [J]. Chinese Journal of Experimental Presentation, 2018(11):16-21.

METHYL LAURATE - Reference Information

FEMA2715 | METHYL LAURATE
LogP5.41 at 36℃
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
use methyl laurate is an important raw material for daily cosmetic essence and soap making industry, and it is also a new type of food emulsifier with high efficiency, safety, non-toxic and pollution-free The raw material of sucrose laurate and the raw material for synthesizing a variety of anionic surfactants and non-ionic surfactants are important intermediates in fine chemical industry.
Used as an intermediate in organic synthesis. Methyl laurate is a flavor ketone produced by the catalyzed reaction of microencapsulated fungal spores. It is also used to produce biodiesel.
Used as gas chromatography stationary liquid, food additive and organic synthesis reagent
gas chromatography analysis standard. Organic synthesis.
Preparation Methyl laurate can be obtained by esterification of lauric acid and methanol. The mixture of lauric acid, anhydrous methanol and concentrated sulfuric acid is heated and refluxed for 18h, and the reaction is poured into water to separate the ester layer. Wash with water, saturated sodium bicarbonate solution and water in turn. After drying, it is distilled, and the 260-263 ℃ fraction is collected, which is methyl diproate.
toxicity GRAS(FEMA).
usage limit FEMA(mg/kg): soft drinks, cold drinks, 0.50~5.0; Candy 0.02-0.50; Baked products 1.0. FDA(§ 1 72.515,2000): Moderate limit.
production method obtained by esterification of lauric acid and methanol. The mixture of lauric acid, anhydrous methanol and concentrated sulfuric acid is heated and refluxed for 18h, and the reaction is poured into water to separate the ester layer. Wash with water, saturated sodium bicarbonate solution and water in turn. After drying, distillation is carried out, and the 260-263 ℃ fraction is collected, which is methyl diproate with 81% yield.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 15:16:47
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View History
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