Methyl Laurate

HCID 8139

Basic information

CAS
111-82-0
Standard SMILES
CCCCCCCCCCCC(=O)OC
InChIKey
UQDUPQYQJKYHQI-UHFFFAOYSA-N
Molecular formula
C13H26O2
Average molar mass
214.34 g/mol
Monoisotopic mass
214.19328007

Overview

Methyl laurate is a fatty acid methyl ester of lauric acid. It has a role as a metabolite. It is a fatty acid methyl ester and a dodecanoate ester.

Names & identifiers

Preferred name
Methyl Laurate
IUPAC
methyl dodecanoate
English name
Methyl laurate
Molecular formula
C13H26O2
Molecular weight
214.34

Names & synonyms

Methyl laurateMETHYL DODECANOATE111-82-0Lauric acid methyl esterDodecanoic acid, methyl esterMethyl laurinateMethyl dodecylateMethyl n-dodecanoateLauric acid, methyl esterUniphat A40Metholene 2296Stepan C40
Show more names
DODECANOIC ACID METHYL ESTERC13H26O2FEMA 2715stepanc40uniphata40Dodecanoic ac
FEMA number 2715FEMA No. 2715DTXSID50268898IPS6BI6KWformyl dodecanoateNSC-5027DTXCID206889CHEBI:87494

Database identifiers

CAS
111-82-0
PubChem CID
8139
DTXSID
DTXSID5026889
ChEMBL
CHEMBL1894365
ChEBI
CHEBI:87494
UNII
8IPS6BI6KW
EC Number
203-911-3
Nikkaji
J374C

Properties

Computed structural properties

XLogP
5.8
Topological polar surface area
26.3 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
11
Heavy atoms
15

Experimental & physicochemical properties

Chemical ClassesOther Classes -> Esters, Other
LipidsFatty Acyls [FA] -> Fatty esters [FA07] -> Short fatty esters [FA0710]
CosmeticsSkin conditioning; Emollient
SpringerMaterials PropertiesBoiling point
FragrancesFragrance Ingredient (Methyl laurate) -> IFRA transparency List
LogP · 2 items

log Kow= 5.41

5.41

Physicochemical properties

Melting point
4 · 4-5 °C (lit.)
Boiling point
262 °C/766 · 262 °C/766 mmHg (lit.)
Density
0.87 g/mL · 0.87 g/mL at 25 °C (lit.)
vapor pressure
0.55 Pa · 0.55Pa at 25℃
FLAVIS Number
9.101 · 09.101 | Methyl dodecanoate
refractive index
20 · n20/D 1.432

Safety & regulation

GHS classification

GHS Classification · 6 items

This chemical does not meet GHS hazard criteria for 12.2% (52 of 426) of reports.

Warning

H400 (74.6%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]

P273, P391, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 426 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Warning

Hazard information

Regulatory Information · 4 items

Chemical: Dodecanoic acid, methyl ester

Dodecanoic acid, methyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Dodecanoic acid, methyl ester are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 04-02-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/14160

Methyl laurate: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Dodecanoic acid, methyl ester: Human health tier I assessment
Hazards SummaryMay cause irritation; [MSDSonline]
FDA Requirements · 1 item

Methyl laurate is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: a) they are used in the minimum quantity required to produce their intended effect, and otherwise in accordance with all the principles of good manufacturing practice, and 2) they consist of one or more of the following, used alone or in combination with flavoring substances and adjuvants generally recognized as safe in food, prior-sanctioned for such use, or regulated by an appropriate section in this part.

EPA Safer ChemicalChemical: Methyl laurate
Hazard Classes and Categories · 4 items

Aquatic Acute 1 (74.6%)

Skin corrosion/irritation - Category 2

Hazardous to the aquatic environment (Acute) - Category 1

Specific target organ toxicity - Single exposure - Category 3 (Narcotic effects)

Safety & protection

Disposal Methods · 1 item

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Toxicology

Interactions · 1 item

Linear saturated fatty acid methyl esters were comitogenic with lectins for mouse lymphocytes, the degree of comitogenicity being strongly dependent on the length of the acyl group, and maximal for methyl tetradecanoate. Lesser effects were found for analogs with 10, 12, or 16 acyl carbon atoms, whereas those with fewer than 10 or more than 16 were inactive. /Methyl esters/

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1,600(SRC), determined from a structure estimation method(2), indicates that methyl dodecanoate is expected to be immobile in soil(SRC). Volatilization of methyl dodecanoate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 0.003 atm-cu m/mole(SRC), using a fragment constant estimation method(3). However, adsorption to soil is expected to attenuate volatilization(SRC). Methyl dodecanoate is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.004 mm Hg(4). Methyl dodecanoate is expected to rapidly biodegrade in aerobic soils by analogy to structurally similar long-chain fatty acid esters(5-7).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1,600(SRC), determined from a structure estimation method(2), indicates that methyl dodecanoate is expected to adsorb to suspended solids and sediment in water(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 0.003 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Volatilization half-lives for a model river and model lake are 5 hours and 6 days, respectively(SRC), using an estimation method(3). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column(SRC). The volatilization half-life from a model pond is estimated to be about 56 hours ignoring adsorption; when considering maximum adsorption the volatilization half-life increases to 14 days(5). According to a classification scheme(6), an estimated BCF of 290(SRC) from its log Kow of 5.41(12) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is high although it may be lower than that indicated due to the expected rapid metabolism rate for this compound(9). Methyl dodecanoate is expected to rapidly biodegrade in aerobic soils by analogy to structurally similar long-chain fatty acid esters(8-10). An estimated base-catalyzed second-order hydrolysis rate constant of 0.030 L/mole-sec(9,SRC) corresponds to half-lives of 7.3 years and 270 days at pH values of 7 and 8, respectively(11).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), methyl dodecanoate, which has a vapor pressure of 0.0041 mm Hg at 25 °C(2), will exist in solely as a vapor in the ambient atmosphere. Vapor-phase methyl dodecanoate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 29 hours(SRC) from its estimated rate constant of 1.3X10-11 cu cm/molecule-sec at 25 °C(3).

Soil Adsorption/Mobility · 1 item

Using a structure estimation method based on molecular connectivity indices(1), the Koc for methyl dodecanoate can be estimated to be about 1600(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl dodecanoate is expected to have low mobility in soil.

Natural Pollution SourcesREPORTED FOUND IN ORRIS ABSOLUTE.
Artificial Pollution SourcesMethyl dodecanoate's production and use as a synthetic intermediate and flavoring(1) may result in its release to the environment through various waste streams(SRC).
Environmental BiodegradationAEROBIC: By analogy to chemically similar long chain fatty acid esters that were rapidly degraded by mixed sewage sludge(1-3), methyl dodecanoate is expected to rapidly biodegrade under aerobic conditions(SRC).

Regulatory information

FDA Requirements · 1 item

Methyl laurate is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: a) they are used in the minimum quantity required to produce their intended effect, and otherwise in accordance with all the principles of good manufacturing practice, and 2) they consist of one or more of the following, used alone or in combination with flavoring substances and adjuvants generally recognized as safe in food, prior-sanctioned for such use, or regulated by an appropriate section in this part.

Safety data

PPE
Eyeshields, Gloves
wgk
1
tsca
TSCA listed
rtecs
OF0670000
ridadr
UN 3082 9 / PGIII
hs_code
2915 90 30

Chemistry & industry

Pharmacology

Cellular LocationsExtracellular

Uses & manufacturing

Uses · 4 items

Made from coconut oil; [Hawley] Used as a flavoring agent and as an intermediate for detergents, emulsifiers, wetting agents, stabilizers, lubricants, plasticizers, textiles, alkanolamides, fatty alcohols, and acids; [HSDB]

Intermediate for detergents, emulsifiers, wetting agents, stabilizers, lubricants, plasticizers, textiles, flavoring

CHEM INT-EG, FOR ALKANOLAMIDES, FATTY ALCOHOLS & ACIDS

FLAVORING AGENT, EG, IN BAKED GOODS & ICE CREAM

U.S. Production2023: 40,000,000 - <55,000,000 lb
Consumer UsesBinder
Industry UsesLubricating agent
Methods of ManufacturingBY PROLONGED BOILING OF LAURIC ACID WITH METHANOL IN THE PRESENCE OF SULFURIC ACID.
Formulations/PreparationsGrades: 69%, 74%, 90%, 96%, 99.8%
Applications · 6 items

DescriptionMethyl laurate has a fatty, floral odor reminiscent of wine. It can be used as a flavor ingredient in foods and pharmaceuticals, and as fragrance in perfumes. As an intermediate, methyl laurate is used for detergents, emulsifier, wetting agents, stabilizers, lubricants, plasticizers, textiles, plastics, and cosmetics. It can also be used as lubricant in textile spin finishes and emollient in cosmetics. It can be used as solvent, co-solvent, oil carrier for agric, pesticides and herbicides. It is also used as defoamer in food-contact coatings and paper/paperboards and it is used in resin-bonded filters for food contact.

DescriptionMethyl laurate has a fatty, floral odor reminiscent of wine. May be prepared by prolonged boiling of lauric acid with methanol in the presence of sulfuric acid. Methyl Laurate is a flavour ketone produced in a reaction biocatalyzed by microencapsulated fungal spores. Also used in production of biodiesel.

OccurrenceReported found in orris absolute, strawberry, apple, bilberry, rum, coconut, grapes, melon, papaya, pineapple, blackberry, mustard, cheeses, hop oil, cognac, white wine, cocoa, oats, plumcot, elderberry juice, loquat, babaco fruit (Carica pentagona Heilborn), Bourbon vanilla, mountain papaya, Chinese cabbage, mussels, cape gooseberry, pawpaw, banana, berries and blue cheese

UsesMethyl dodecanoate used in production of biodiesel. It has been used in selective synthesis of the secondary amide surfactant, N-methyl lauroylethanolamide. It is also utilized as emollients, perfuming agents skin conditioning.

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

General DescriptionHydrogenation 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.

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Hong Kong Tiansheng New Material Trading Co., Ltd+8617320695765 · [email protected]
河北创海生物科技有限公司+86-86-13131129325 · [email protected]

Additional notes

DefinitionChEBI: A fatty acid methyl ester of lauric acid.

Related reactions

11 records

Compound notes

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