linoleamide MEA

9,12-octadecadienamide, N-(2-hydroxyethyl)-, (9Z,12Z)-

CAS: 68171-52-8 C20 H37 N O2 MW: 323.52029000

Identification

Namelinoleamide MEA
CAS Number68171-52-8
EINECS269-029-6
FDA UNII889DYX0816
Molecular FormulaC20 H37 N O2
Molecular Weight323.52029000
MDL NumberMFCD00674434

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 499.06 °C. @ 760.00 mm Hg (est)
Flash Point 492.00 °F. TCC ( 255.60 °C. ) (est)
logP (o/w) 6.003 (est)
Soluble in water, 0.108 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesantistatic agents

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorycosmetic agents
Recommendation for linoleamide MEA usage levels up tonot for fragrance use.
Recommendation for linoleamide MEA flavor usage levels up tonot for flavor use.

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Potential Uses

antistatic agents viscosity controlling agents

Natural Occurrence

not found in nature

Synonyms

mono ethanolamine linoleic acid amide 9-(Z),12-(Z)-N-(2- hydroxyethyl) octadeca-9,12-dien-1-amide N-(2- hydroxyethyl)-linoleamide N-(2- hydroxyethyl)linoleamide (9Z,12Z)-N-(2- hydroxyethyl)octadeca-9,12-dienamide linoleic ethanolamide linoleoyl ethanolamide linoleoyl monoethanolamide linoleoylethanolamide (9Z,12Z)- octadeca-9,12-dienoic acid (2-hydroxy-ethyl)-amide 9,12- octadecadienamide, N-(2-hydroxyethyl)-, (9Z,12Z)- N-(9Z,12Z- octadecadienoyl)-ethanolamine N-cis-9-cis-12- octadecadienoylethanolamine (9Z,12Z)-N-(2- xhydroxyethyl)octadeca-9,12-dien-1-amide PubMed: Dietary non-esterified oleic Acid decreases the jejunal levels of anorectic N-acylethanolamines. PubMed: Simultaneous ultra-high performance liquid chromathograpy-electrospray ionization-quadrupole-time of flight mass spectrometry quantification of endogenous anandamide and related N-acylethanolamides in bio-matrices. PubMed: Role of anorectic N-acylethanolamines in intestinal physiology and satiety control with respect to dietary fat. PubMed: Classical endocannabinoid-like compounds and their regulation by nutrients. PubMed: Troubleshooting in LC-MS/MS method for determining endocannabinoid and endocannabinoid-like molecules in rat brain structures applied to assessing the brain endocannabinoid/endovanilloid system significance. PubMed: Effect of diet on tissue levels of palmitoylethanolamide. PubMed: Quantitative analysis of multiple fatty acid ethanolamides using ultra-performance liquid chromatography-tandem mass spectrometry. PubMed: Lauroylethanolamide and linoleoylethanolamide improve functional outcome in a rodent model for stroke. PubMed: Dietary fat decreases intestinal levels of the anorectic lipids through a fat sensor. PubMed: N-acylethanolamines, anandamide and food intake. PubMed: Influence of dietary fatty acids on endocannabinoid and N-acylethanolamine levels in rat brain, liver and small intestine. PubMed: Food intake regulates oleoylethanolamide formation and degradation in the proximal small intestine. PubMed: Intestinal levels of anandamide and oleoylethanolamide in food-deprived rats are regulated through their precursors. PubMed: Anandamide and 2-arachidonoylglycerol inhibit fatty acid amide hydrolase by activating the lipoxygenase pathway of the arachidonate cascade. PubMed: Anandamide induces apoptosis in human cells via vanilloid receptors. Evidence for a protective role of cannabinoid receptors. PubMed: Cannabinoid mimics in chocolate utilized as an argument in court. PubMed: Anandamide activates human platelets through a pathway independent of the arachidonate cascade. PubMed: Anandamide hydrolysis by human cells in culture and brain. PubMed: Dioxygenation of N-linoleoyl amides by soybean lipoxygenase-1.