We have found 46587 results matching your criteria.
Please wait while we search...

General Material Information

Preferred name (Z)-oleic acid
Trivial Name Oleic acid
Short Description (Z)-9-octadecenoic acid
Formula C18 H34 O2
CAS Number 112-80-1
FEMA Number 2815
Flavis Number 8.013
ECHA Number 204-007-1
FDA UNII 2UMI9U37CP
Nikkaji Number J2.460K
Beilstein Number 1726542
MDL MFCD00064242
COE Number 13
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 333 (Z)-oleic acid
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 112-80-1 ; OLEIC ACID
Synonyms
  • distoline
  • edenor ATiO5
  • edenor FTiO5
  • (Z)- elaidic acid
  • cis- elaidic acid
  • emersol 205
  • emersol 210
  • emersol 211
  • emersol 213
  • emersol 214NF
  • emersol 233
  • emersol 6313NF
  • emersol 6321
  • emersol 6333 NF
  • emersol 7021
  • extraolein 90
  • glycon RO
  • glycon WO
  • groco 2
  • groco 4
  • groco 5L
  • groco 6
  • hy-phi 1055
  • hy-phi 1088
  • hy-phi 2066
  • hy-phi 2088
  • hy-phi 2102
  • industrene 104
  • industrene 105
  • industrene 205
  • industrene 206
  • lunac O-CA
  • lunac O-LL
  • lunac OA
  • metaupon
  • neo-fat 90-04
  • neo-fat 92-04
  • (9Z)- octadec-9-enoic acid
  • (Z)- octadec-9-enoic acid
  • cis- octadec-9-enoic acid
  • (Z)- octadeca-9-enoic acid
  • (Z)-9-octadecanoic acid
  • cis-9-octadecanoic acid
  • (9Z)- octadecenoic acid
  • (9Z)-9-octadecenoic acid
  • (Z)-9-octadecenoic acid
  • 9-(Z)- octadecenoic acid
  • 9-cis- octadecenoic acid
  • cis-9-octadecenoic acid
  • 9-octadecenoic acid (9Z)-
  • 9-octadecenoic acid (Z)-
  • 9-octadecenoic acid, (9Z)-
  • 9-octadecenoic acid, (Z)-
  • 9-octadecenoic acid, cis-
  • oelsaeure
  • oelsauere
  • oleic acid
  • cis- oleic acid
  • delta9-cis- oleic acid
  • oleic acid 65%--no BHA/BHT added
  • oleic acid N.F.
  • oleic acid natural
  • oleic acid, natural & kosher
  • oleine 7503
  • oleinic acid
  • pamolyn
  • pamolyn 100
  • pamolyn 100 FGK kosher oleic acid
  • pamolyn 125
  • priolene 6900
  • priolene 6906
  • priolene 6907
  • priolene 6928
  • priolene 6930
  • priolene 6933
  • priolene 6936
  • tego-oleic 130
  • vopcolene 27
  • wecoline OO
  • wochem no. 320
  • (Z)-octadec-9-enoic acid
  • 9-Octadecenoic acid (9Z)-
  • 9-Octadecenoic acid (Z)-
  • (9Z)-9-Octadecenoic acid
  • cis-Δ9-Octadecenoic acid
  • cis-9-Octadecenoic acid
  • Δ9-cis-Oleic acid
  • cis-Oleic acid
  • Z-9-Octadecenoic acid
  • 9-Octadecenoic acid, (Z)-
  • Δ9-cis-Octadecenoic acid
  • 9-cis-Octadecenoic acid
  • C18:1
  • Lunac O-P
  • NAA 35
  • Extra Olein 80
  • Extra Oleic 99
  • Emersol 213NF
  • Extra Olein 90R
  • Extra Olein 99
  • Extra Oleic 90
  • Extra Oleic 80R
  • D 100
  • D 100 (fatty acid)
  • 9Z-Octadecenoic acid
  • NAA 38
  • Priolene 6204
  • Crossential O 94
  • Extra Olein A 1981
  • Lunac O-V
  • B 115
  • Crodacid O-P
  • Clear FRAC EF
  • Extra Olein 90
  • NAA 36
  • NAA 200
  • Lunac O-LL-V
  • Emersol 622
  • Lunac LO-V
  • C18:1n9c
  • Edenor C 18:1-98-100
  • PM 500
  • PM 810B
  • Extra Olein 80R
  • Palmera A 1813
  • Radiacid 0137
  • Lubolic acid
  • (18,9-Olefin) oleic acid
  • Impex
  • Radiacid 0212
  • POFAC 930
  • Priolene 6977
  • MeSH ID: D019301
  • Kortacid 1811
  • CU-A (fatty acid)
  • CU-A
  • OA 7075

US / EU / FDA / JECFA / FEMA / Scholar / Patents

Google Scholar Start search
Google Books Start search
Google Patents Start search
Perfumer & Flavorists Start search
EU Patents Start search
PubMeb Start search
NCBI Start search

Literature & References

(Z)-octadec-9-enoic acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:112-80-1
Pubchem (cid):445639
Pubchem (sid):134973687
Flavornet:112-80-1
Pherobase:View
Publications by PubMed
Perturbation of copper homeostasis is instrumental in early developmental arrest of intraerythrocytic Plasmodium falciparum.
Oxygenated fatty acids isolated from wheat bran slurries.
Δ12-Fatty acid desaturase from Candida parapsilosis is a multifunctional desaturase producing a range of polyunsaturated and hydroxylated fatty acids.
Acinetobacter harbinensis sp. nov., isolated from river water.
Optimization of lipid enriched biomass production from oleaginous fungus using response surface methodology.
Baseline resolution of isomers by traveling wave ion mobility mass spectrometry: investigating the effects of polarizable drift gases and ionic charge distribution.
Cis-9-octadecenoic acid from the rhizospheric bacterium Stenotrophomonas maltophilia BJ01 shows quorum quenching and anti-biofilm activities.
Inhibition of Mycobacterium tuberculosis PknG by non-catalytic rubredoxin domain specific modification: reaction of an electrophilic nitro-fatty acid with the Fe-S center.
Liquid chromatography-mass spectrometry-based chemotaxonomic classification of Aspergillus spp. and evaluation of the biological activity of its unique metabolite, neosartorin.
The rhizobacterium Arthrobacter agilis produces dimethylhexadecylamine, a compound that inhibits growth of phytopathogenic fungi in vitro.
Characterization and chemical composition of fatty acids content of watermelon and muskmelon cultivars in Saudi Arabia using gas chromatography/mass spectroscopy.
Triterpene esters and biological activities from edible fruits of Manilkara subsericea (Mart.) Dubard, Sapotaceae.
Acinetobacter puyangensis sp. nov., isolated from the healthy and diseased part of Populus xeuramericana canker bark.
Antifungal hydroxy fatty acids produced during sourdough fermentation: microbial and enzymatic pathways, and antifungal activity in bread.
Hydroxyl octadecenoic acids biosynthesized by crown galls of Panax quinquefolium induced by artermisinic acid.
Assessment and profiling of the fatty acids in two ackee fruit (Blighia sapida Köenig) varieties during different ripening stages.
In Silico Studies on Fungal Metabolite against Skin Cancer Protein (4,5-Diarylisoxazole HSP90 Chaperone).
A study on fatty acids in seeds of Euterpe oleracea Mart seeds.
Chemical composition and biological activity of Salvia verbenaca essential oil.
Composition of fatty oils from semen ziziphi spinosae and its cardiotonic effect on isolated toad hearts.
Fast ultrasound-assisted extraction of polar (phenols) and nonpolar (lipids) fractions in Heterotheca inuloides Cass.
[Comparison of organic component and di-n-butyl phthalate between human milk and cow milk products].
Three new fatty acids from the roots of Boehmeria nivea (L.) Gaudich and their antifungal activities.
Identification of urinary sex pheromones in female buffaloes and their influence on bull reproductive behaviour.
Chemical composition and bioactivities of the marine alga Isochrysis galbana from Taiwan.
[Preparation of Ganoderma lucidum polysaccharides and triterpenes microemulsion and its anticancer effect in mice with transplant Heps tumors].
Identification of three genes encoding microsomal oleate desaturases (FAD2) from the oilseed crop Camelina sativa.
Genetic variants in the FADS gene cluster are associated with arachidonic acid concentrations of human breast milk at 1.5 and 6 mo postpartum and influence the course of milk dodecanoic, tetracosenoic, and trans-9-octadecenoic acid concentrations over the duration of lactation.
Plasmodium falciparum: differing effects of non-esterified fatty acids and phospholipids on intraerythrocytic growth in serum-free medium.
Paleic acid, a fatty acid from Paenibacillus sp.: taxonomy, fermentation, isolation, structure determination, and anti-Mannheimia and -Pasteurella activity.
Variation in amino acid and lipid composition of latent fingerprints.
Effects of oil source and fish oil addition on ruminal biohydrogenation of fatty acids and conjugated linoleic acid formation in beef steers fed finishing diets.
Polyunsaturated docosahexaenoic acid suppresses oxidative stress induced endothelial cell calcium influx by altering lipid composition in membrane caveolar rafts.
Chemical composition and in vitro antimicrobial activity of the volatile oils from Gliomastix murorum and Pichia guilliermondii, two endophytic fungi in Paris polyphylla var. yunnanensis.
Oxidation of oleic acid at the air-water interface and its potential effects on cloud critical supersaturations.
An ab initio and DFT study of structure and vibrational spectra of gamma form of oleic acid: comparison to experimental data.
Two new compounds from transgenic Panax quinquefolium.
[GC-MS analysis on the chemical constituents of essential oil from bark of Horsfieldia hainanensis].
Fabrication of superparamagnetic magnetite/poly(styrene-co-12-acryloxy-9-octadecenoic acid) nanocomposite microspheres with controllable structure.
[Identification and antibacterial activity of secondary metabolites from Taxus endophytic fungus].
Characterization of probiotic carnobacteria isolated from rainbow trout (Oncorhynchus mykiss) intestine.
Thermodynamics of the clusterization process of cis isomers of unsaturated fatty acids at the air/water interface.
Infrared spectroscopic study of the effect of oleic acid on the deliquescence behaviour of ammonium sulfate aerosol particles.
GC-MS analysis of liposoluble constituents from the stems of Cynomorium songaricum.
Metabolic profiling of transgenic rice with cryIAc and sck genes: an evaluation of unintended effects at metabolic level by using GC-FID and GC-MS.
Studies on chemical constituents of Gracilaria verrucosa.
Identification of acylglycerols containing dihydroxy fatty acids in castor oil by mass spectrometry.
Antioxidant, alpha-amylase inhibitory and brine-shrimp toxicity studies on Centaurea centaurium L. methanolic root extract.
Two new fatty esters from Rhazya stricta roots (Apocynanaceae).
Liposomal formulations from phospholipids of Greek almond oil. Properties and biological activity.
Plasmodium falciparum: Chemically defined medium for continuous intraerythrocytic growth using lipids and recombinant albumin.
Possible involvement of long chain fatty acids in the spores of Ganoderma lucidum (Reishi Houshi) to its anti-tumor activity.
[Analysis of the volatile oils chemical constituents of roots of Actinidia deliciosa].
A novel preparation of surface-modified paramagnetic magnetite/polystyrene nanocomposite microspheres by radiation-induced miniemulsion polymerization.
Acinetobacter soli sp. nov., isolated from forest soil.
Impact of oleic acid (cis-9-octadecenoic acid) on bacterial viability and biofilm production in Staphylococcus aureus.
[Dynamic changes of cold-resistant substances of overwintering Chilo suppressalis (Walker) larvae].
New bioactive fatty acids.
Ricinoleic acid in common vegetable oils and oil seeds.
Tetrasphaera remsis sp. nov., isolated from the Regenerative Enclosed Life Support Module Simulator (REMS) air system.
Second-order standard addition for deconvolution and quantification of fatty acids of fish oil using GC-MS.
Tetrahydrofurandiols (THF-diols), leukotoxindiols (LTX-diols), and endocrine disruption in rats.
Isolation of fatty acids with anticancer activity from Protaetia brevitarsis larva.
Aeromicrobium tamlense sp. nov., isolated from dried seaweed.
Structural analysis of oligomeric molecules formed from the reaction products of oleic acid ozonolysis.
Vesicles from docosahexaenoic acid.
Lipid microencapsulation in starch.
Kinetic studies of the interaction of fatty acids with phosphatidylcholine vesicles (liposomes).
Leukotoxin diols from ground corncob bedding disrupt estrous cyclicity in rats and stimulate MCF-7 breast cancer cell proliferation.
Production of conjugated fatty acids by lactic acid bacteria.
Polyamines are essential for the synthesis of 2-ricinoleoyl phosphatidic acid in developing seeds of castor.
[Analysis of ant oil extracted with supercritical CO2 fluid from Polyrhachis vicina by GC-MS].
Long-chain fatty acids increase cellular dopamine in an immortalized cell line (MN9D) derived from mouse mesencephalon.
The novel pathway for ketodiene oxylipin biosynthesis in Jerusalem artichoke (Helianthus tuberosus) tubers.
Chemical composition of the essential oils of two Alpinia species from Hainan Island, China.
Gas chromatography-mass spectrometry of cis-9,10-epoxyoctadecanoic acid (cis-EODA). II. Quantitative determination of cis-EODA in human plasma.
Ethanol-mediated variations in cellular fatty acid composition and protein profiles of two genotypically different strains of Escherichia coli O157:H7.
Two distinct pathways for the formation of hydroxy FA from linoleic acid by lactic acid bacteria.
Linoleic acid epoxide promotes the maintenance of mitochondrial function and active Na+ transport following hypoxia.
Solid-liquid phase behavior of binary fatty acid mixtures. 2. Mixtures of oleic acid with lauric acid, myristic acid, and palmitic acid.
Band analysis of temperature-dependent near-infrared spectra of oleic acid in the pure liquid state by the analytic geometric approach.
Characterisation of castor oil by on-line and off-line non-aqueous reverse-phase high-performance liquid chromatography-mass spectrometry (APCI and UV/MALDI).
Acute toxicity of fatty acids to the freshwater green alga Selenastrum capricornutum.
Fatty acid composition of seeds of Satureja thymbra and S. cuneifolia.
An investigation into the role of calcium in the modulation of rat synaptosomal D-[3H]aspartate transport by docosahexaenoic acid.
NTP Toxicology and Carcinogenesis Studies of Oleic Acid Diethanolamine Condensate (CAS No. 93-83-4) in F344/N Rats and B6C3F1 Mice (Dermal Studies).
Gas chromatography-mass spectrometry of cis-9,10-epoxyoctadecanoic acid (cis-EODA). I. Direct evidence for cis-EODA formation from oleic acid oxidation by liver microsomes and isolated hepatocytes.
Repellent activity of constituents identified in Foeniculum vulgare fruit against Aedes aegypti (Diptera: Culicidae).
Lipid content and fatty acid composition in lemon wax.
Attractant volatiles released by female and male Triatoma infestans (Hemiptera: Reduviidae), a vector of chagas disease: chemical analysis and behavioral bioassay.
Identification and total synthesis of novel fatty acids from the Siphonarid limpet Siphonaria denticulata.
The cytotoxicity and chemical constituents of the hexane fraction of Typhonium flagelliforme (Araceace).
Natural oviposition-deterring chemicals in female cotton bollworm, Helicoverpa armigera (Hubner).
[Branched alkanes and other apolar compounds produced by the cyanobacterium Microcoleus vaginatus from the Negev desert].
Transgenic expression of a delta 12-epoxygenase gene in Arabidopsis seeds inhibits accumulation of linoleic acid.
In vitro test for the effectiveness of antioxidants as inhibitors of thiyl radical-induced reactions with unsaturated fatty acids.
Defining mechanisms of toxicity for linoleic acid monoepoxides and diols in Sf-21 cells.
Analysis of the toxic effects of linoleic acid, 12,13-cis-epoxyoctadecenoic acid, and 12,13-dihydroxyoctadecenoic acid in rabbit renal cortical mitochondria.
Transformations of 12,13-epoxy-11-hydroxy-9-octadecenoic acid and 4,5-epoxy-N-acetylsphingosine by incubation with liver homogenate and liver microsomes.
Inhibition of polyunsaturated fatty acid accumulation in plants expressing a fatty acid epoxygenase.
Monohydroxylation and esterification as determinants of the effects of cis- and trans-9-octadecenoic acids on the permeation of hydrocortisone and 5-fluorouracil across hairless mouse skin in vitro.
Behenic acid is a cholesterol-raising saturated fatty acid in humans.
Biotransformation of linoleic acid by Clavibacter sp. ALA2: heterocyclic and heterobicyclic fatty acids.
Antinociceptive activity of ricinoleic acid, a capsaicin-like compound devoid of pungent properties.
Dietary stearic acid reduces cholesterol absorption and increases endogenous cholesterol excretion in hamsters fed cereal-based diets.
The action of soybean lipoxygenase-1 on 12-iodo-cis-9-octadecenoic acid: the importance of C11-H bond breaking.
Quality characteristics of Canarium schweinfurthii Engl. oil.
Involvement of the cis/trans isomerase Cti in solvent resistance of Pseudomonas putida DOT-T1E.
Substrate selectivity of various lipases in the esterification of cis- and trans-9-octadecenoic acid.
Conversion of unsaturated fatty acids by bacteria isolated from compost.
Influence of oleic acid on the expression, activation and activity of gelatinase A produced by oncogene-transformed human bronchial epithelial cells.
In vivo studies of the biosynthesis of vernolic acid in the seed of Vernonia galamensis.
Codiffusion of propylene glycol and dimethyl isosorbide in hairless mouse skin.
Hydration of linoleic acid by bacteria isolated from ruminants.
Long-chain alkenes of the haptophytes Isochrysis galbana and Emiliania huxleyi.
Strong dependence of the lipid peroxidation product spectrum whether Fe2+/O2 or Fe3+/O2 is used as oxidant.
Skin penetration enhancing action of cis-unsaturated fatty acids with omega-9, and omega-12-chain lengths.
Identification of non-heme diiron proteins that catalyze triple bond and epoxy group formation.
Lipoproteins of Treponema denticola: their effect on human polymorphonuclear neutrophils.
Intestinal absorption of Mn-mesoporphyrin in a small bowel sac system: effect of oleic acid.
Mechanism of linoleic acid hydroperoxide reaction with alkali.
Production of hydroxy fatty acid (10-hydroxy-12(Z)-octadecenoic acid) by Lactobacillus plantarum from linoleic acid and its cardiac effects to guinea pig papillary muscles.
Fat infiltration in liver of rats induced by different dietary plant oils: high oleic-, medium oleic- and high petroselinic acid-oils.
Lipid oxidation products in ischemic porcine heart tissue.
Glucuronic acid-conjugated dihydroxy fatty acids in the urine of patients with generalized peroxisomal disorders.
Analysis by fast-atom bombardment tandem mass spectrometry of phosphatidylcholine isolated from heart mitochondrial fractions: Evidence of incorporation of monohydroxylated fatty acyl moieties.
Pre-incubation of synaptosomes with arachidonic acid potentiates inhibition of [3H]D-aspartate transport.
Fatty acid selectivity of a lipase purified from Vernonia galamensis seed.
Interaction of manganese-mesoporphyrin with oleic acid vesicles.
Action of soybean lipoxygenase 1 on 12-iodo-cis-9-octadecenoic acid and 12-bromo-cis-9-octadecenoic acid.
Trans-9-octadecenoic acid is biologically neutral and does not regulate the low density lipoprotein receptor as the cis isomer does in the hamster.
Nitric oxide reductase from Pseudomonas stutzeri, a novel cytochrome bc complex. Phospholipid requirement, electron paramagnetic resonance and redox properties.
Heating unsaturated fatty acids in air produces hemagglutinins.
Cellular fatty acid composition of Erysipelothrix rhusiopathiae and Erysipelothrix tonsillarum.
Plasma cholesteryl ester transfer protein activity is increased when trans-elaidic acid is substituted for cis-oleic acid in the diet.
Solvent effects on lipase-catalyzed esterification of glycerol and fatty acids.
Validation of reflectance infrared spectroscopy as a quantitative method to measure percutaneous absorption in vivo.
Fatty acids regulate hepatic low density lipoprotein receptor activity through redistribution of intracellular cholesterol pools.
Differential effects of cis and trans fatty acid isomers, oleic and elaidic acids, on the cholesteryl ester transfer protein activity.
Metabolism of 12(S)-hydroxy-5,8,10,14-eicosatetraenoic acid and other hydroxylated fatty acids by the reductase pathway in porcine polymorphonuclear leukocytes.
Mammalian pheromones VIII Chemical characterization of preorbital gland secretion of grey duiker,Sylvicapra grimmia (Artiodactyla: Bovidae).
[Volatile components of herbal Cynomorii].
Inactivation of soybean lipoxygenase 1 by 12-iodo-cis-9-octadecenoic acid.
Identification of major lipids from the scent gland secretions of Dumeril's ground boa (Acrantophis dumerili Jan) by gas chromatography-mass spectrometry.
Development of plant cuticles: fine structure and cutin composition of Clivia miniata Reg. leaves.
Metabolism in humans of cis-12,trans-15-octadecadienoic acid relative to palmitic, stearic, oleic and linoleic acids.
Metabolism of cis-12-octadecenoic acid and trans-9,trans-12-octadecadienoic acid and their influence on lipogenic enzyme activities in mouse liver.
Activities of liver mitochondrial and peroxisomal fatty acid oxidation enzymes in rats fed trans fat.
Oxidation and esterification of geometrical and positional isomers of octadecenoic acids in perfused rat liver.
Isolation and identification of 1(3),2-diacylglyceryl-(3)-O-4'-(N,N,N-trimethyl)homoserine from the soil amoeba, Acanthamoeba castellanii.
Absorption and distribution of deuterium-labeled trans- and cis-11-octadecenoic acid in human plasma and lipoprotein lipids.
Strain dependence of the metabolism of cis- and trans-isomers of 9-octadecenoic acid in perfused liver and cell-free preparation in rats.
[Inhibition of methanogenesis in the rumen of sheep. II. Methanogenesis after administration of inhibitors].
Fluorescent pigments by covalent binding of lipid peroxidation by-products to protein and amino acids.
Synthesis and biological assessment of long-acting estradiol fatty acid esters in ovariectomized rats.
In vivo distribution and turnover of trans- and cis-10-octadecenoic acid isomers in human plasma lipids.
Conversion of linoleic acid hydroperoxide to hydroxy, keto, epoxyhydroxy, and trihydroxy fatty acids by hematin.
Structure-activity relationship of unsaturated fatty acids as mosquito ovipositional repellents.
Coupling between fatty acid binding and sulfhydryl oxidation in bovine serum albumin.
Analysis of 1,2-diols of linoleic, alpha-linolenic and arachidonic acid by gas chromatography--mass spectrometry using cyclic alkyl boronic esters.
Incorporation of deuterium-labeled trans- and cis-13-octadecenoic acids in human plasma lipids.
Levels of oxygenated Fatty acids in young corn and sunflower plants.
Oscillatoria Sp. (Cyanophyta) mat metabolites implicated in habitat selection inBembidion obtusidens (Coleoptera: Carabidae).
Metabolism of linoleic Acid by barley lipoxygenase and hydroperoxide isomerase.
Degradation of linoleic acid hydroperoxides by a cysteine . FeCl3 catalyst as a model for similar biochemical reactions. III. A novel product, trans-12,13-epoxy-11-oxo-trans-9-octadecenoic acid, from 13-L (S)-hydroperoxy-cis-9,trans-11-octadecadienoic acid.
Degradation of linoleic acid hydroperoxides by a cysteine . FeCl3 catalyst as a model for similar biochemical reactions. II. Specificity in formation of fatty acid epoxides.
Formation of (n-9) and (n-7) cis-monounsaturated fatty acids in seeds of higher plants.
Distribution of deuterium-labeled cis- and trans-12-octadecenoic acids in human plasma and lipoprotein lipids.
15-hydroxy-5,8,11,13-eicosatetraenoic acid: A potent and selective inhibitor of platelet lipoxygenase.
Chain elongation of trans-octadecenoic acid isomers in rat liver microsomes.
Incorporation of deuterium labeled cis- and trans-9-octadecenoic acid in humans: plasma, erythrocyte, and platelet neutral lipids.
Fatty acid composition of Simonsiella strains.
The effect of octadecenoic acid on the growth of japanese encephalitis virus in Novikoff hepatoma cells.
Positional specificity of gamma-ketol formation from linoleic acid hydroperoxides by a corn germ enzyme.
Replacement of acyl and alk-1-enyl groups in Clostridium butyricum phospholipids by exogenous fatty acids.
Effect of fatty acids on growth of Japanese encephalitis virus cultivated in BHK-21 cells and phospholipid metabolism of the infected cells.
Decomposition of unsaturated fatty acid hydroperoxides by hemoglobin: Structures of major products of 13L-hydroperoxy-9,11-octadecadienoic acid.
A comparison of the metabolism of geometrical isomers of 14 C- 9 -octadecenoic acid in threonine-imbalanced rats.
Lipids of Treponema pallidum Kazan 5.
Sequential enzymes of linoleic acid oxidation in corn germ: lipoxygenase and linoleate hydroperoxide isomerase.
Effect of isomeric cis-octadecenoic acids on the growth of Leptospira interrogans serotype patoc.
The enzymic conversions of 13-hydroperoxy-cis-9-trans-11-octadecadienoic acid into 13-hydroxy-12-oxo-cis-9-octadecenoic acid.
The catabolism of the geometric isomers of uniformly 14C-labeled delta 9-octadecenoic acid and uniformly 14C-labeled delta 9,12-octadecadienoic acid by the fasting rat.
Oxidation of the geometric isomers of delta 9-octadecenoic acid by rat-liver mitochondria.
[ON THE SYNTHESIS OF (8-C14)-CIS-DELTA-9-OCTADECENOIC ACID].

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
UM BBD:Search
KEGG (GenomeNet):C00712
HMDB (The Human Metabolome Database):HMDB00207
FooDB:FDB012858
YMDB (Yeast Metabolome Database):YMDB00131
Export Tariff Code:2916.15.1000
FDA Listing of Food Additive Status:View
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 282.46737670898
Specific gravity @ 25 °C
Pounds per Gallon 7.339 to 7.414
Refractive Index 1.4595 to 1.464 @ 20 °C
Melting Point 13 to 14°C @ 760 mm Hg
Boiling Point 194 to 195°C @ 1.2 mm Hg
Vapor Pressure 1 mmHg @ 176 °C
Flash Point TCC Value 112.78 °C TCC
logP (o/w) 7.698 est
Solubility
paraffin oil Yes
water, 0.01151 mg/L @ 25 °C (est) Yes

Organoleptic Properties

Odor Type: Fatty
fatty, waxy, lard, fried, oily, tallow, savory
Odor strength low
General comment At 100.00 %. faint fatty waxy lard fried
Mosciano, Gerard P&F 26, No. 3, 80, (2001) At 5.00 %. Oily, waxy with lard and tallow notes. It has a fried savory nuance
Flavor Type: Fatty
fatty, vegetable, oily, lard, tallow, fried, potato
Mosciano, Gerard P&F 26, No. 3, 80, (2001) At 10.00 - 20.00 ppm. Fatty, vegetable oil with lard and tallow nuances of french fried potatoes

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50 25000 mg/kg
Toksikologicheskii Vestnik. Vol. (1), Pg. 39, 2000.

oral-rat LD50 > 5000 mg/kg
(Moreno, 1977b)

oral-rat LD50 > 19000 mg/kg
LD50 was > 21.5 ml for ocadecanoic acid (75 % oleic acid) and octadecadienoic acid (53 % linoleic acid, 23 % oleic acid).
(Briggs et al., 1976)

intraperitoneal-mouse LD50 282 mg/kg
Yakugaku Zasshi. Journal of Pharmacy. Vol. 104, Pg. 793, 1984.

oral-mouse LD50 28000 mg/kg
Toksikologicheskii Vestnik. Vol. (1), Pg. 39, 2000.

intravenous-mouse LD50 230 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Acta Pharmacologica et Toxicologica. Vol. 18, Pg. 141, 1961.

intravenous-rabbit LD > 55 mg/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
American Review of Respiratory Disease. Vol. 137(Suppl), Pg. 226, 1988.

intravenous-rat LD50 2400 ug/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA
American Journal of Pathology. Vol. 103, Pg. 376, 1981.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
thickeners, gelling agents, stabalizers and emulsifiers
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for (Z)-oleic acid usage levels up to:
6.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 830.00 (μg/capita/day)
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -25.00000
beverages(nonalcoholic): 0.250000.40000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: -0.02000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -30.00000
fruit ices: -30.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -3.50000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 6 (FGE.06): Straight-and branched-chain aliphatic unsatured primary alcohols, aldehydes, carboxylic acids, and esters from chemical groups 1 and 4
View page or View pdf

Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission related to Flavouring Group Evaluation 5: Esters of 23 branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and 24 branched- and straight-chain unsaturated carboxylic acids from chemical groups 1, 2, and 5
View page or View pdf

Flavouring Group Evaluation 6, Revision 1 (FGE.06Rev1) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Flavouring Group Evaluation 5, Revision 1 (FGE.05Rev1):Esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids from chemical groups 1, 2, and 5 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) [1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Flavouring Group Evaluation 62 (FGE.62) Consideration of linear and branched-chain aliphatic unsaturated, unconjugated alcohols, aldehydes, acids, and related esters evaluated by JECFA (61st meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05 (2005) and to straight- and branched-chain aliphatic unsaturated primary alcohols, aldehydes, carboxylic acids, and esters evaluated by EFSA in FGE.06 (2004) (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 71: Consideration of aliphatic, linear, alpha,beta-unsaturated carboxylic acids and related esters
View page or View pdf

Flavouring Group Evaluation 72 (FGE.72): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids. Esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2 (2010)
View page or View pdf

Flavouring Group Evaluation 5, Revision 2 (FGE.05Rev2): Branched- and straight-chain unsaturated carboxylic acids and esters of these with aliphatic saturated alcohols from chemical groups 1, 2, 3 and 5
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 95 (FGE.95): Consideration of aliphatic, linear or branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (69th meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05Rev1 (2008)
View page or View pdf

Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species
View page or View pdf

Review of substances/agents that have direct beneficial effect on the environment: mode of action and assessment of efficacy
View page or View pdf

Re-evaluation of fatty acids (E 570) as a food additive
View page or View pdf

EPI System: View
ClinicalTrials.gov:search
NIOSH International Chemical Safety Cards:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):112-80-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :445639
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
(Z)-octadec-9-enoic acid
Chemidplus:0000112801
EPA/NOAA CAMEO:hazardous materials
RTECS:112-80-1