Oleic Acid

    • Product Name: Oleic Acid
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
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    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code
    Product Name Oleic Acid
    Iupac Name (9Z)-Octadec-9-enoic acid
    Chemical Formula C18H34O2
    Molecular Weight 282.46 g/mol
    Cas Number 112-80-1
    Ec Number 204-007-1
    Appearance Colorless to pale yellow liquid
    Odor Mild fatty odor
    Melting Point 13-16 °C
    Boiling Point 360 °C
    Density 0.895 g/cm³ at 25 °C
    Solubility Insoluble in water; soluble in ethanol, ether, chloroform, and oils
    Flash Point 189 °C
    Refractive Index 1.4585 at 20 °C
    Viscosity 25.6 mPa·s at 25 °C
    Pka 9.85

    As an accredited Oleic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Oleic Acid is packaged in a 500 mL amber glass bottle with a secure screw cap for safe chemical storage.
    Container Loading (20′ FCL) 20′ FCL container loading of Oleic Acid: liquid chemical packed in drums or flexitank, secured, labeled, and sealed for ocean shipment.
    Shipping Oleic acid is generally shipped as a non-hazardous, combustible liquid in steel drums, IBC totes, or bulk tank trucks/ISO tanks. Containers should be closed, kept away from heat, sparks, and strong oxidizers. For bulk shipments, insulated or heated tanks may be required to maintain flowability. Standard transport documentation applies.
    Storage Store oleic acid in a cool, dry, well-ventilated area away from heat, ignition sources, and strong oxidizers. Keep containers tightly closed and protected from light and moisture. Use compatible containers such as glass, stainless steel, or high-density polyethylene. Maintain moderate temperatures, preferably above 16°C, to prevent solidification. Label clearly and inspect regularly for leaks or degradation. Store separately from incompatible materials.
    Shelf Life About 2 years when stored tightly sealed, cool, dark, and under inert gas; oleic acid oxidizes upon air exposure.
    Application of Oleic Acid
    On false-twist texturing machines operating at spindle speeds above 10,000 rpm, spin finish formulations applied to partially oriented polyester yarn must control fiber-to-metal friction without decomposing in heat-setting ovens. Oleic acid is incorporated at 2-8 wt% in mineral oil or synthetic ester carrier blends. Acid value is held at 5-15 mg KOH/g per ASTM D974 or ISO 660. Iodine value is maintained at 85-95 g I2/100 g per ISO 3961 to limit oxidative breakdown at heater box temperatures above 200°C. Emulsion stability of a 5% aqueous dilution is checked for 24 h at 25°C; oil separation above 2 vol% triggers batch rejection. On high-speed draw-twisting frames, excessive free oleic acid migrates to guide surfaces and forms varnish; therefore esterified oleic acid or ethoxylated oleate esters replace the free acid when fiber finish pickup exceeds 0.4 wt% on yarn. Neutralized oleic acid with diethanolamine at 1:1 molar ratio reduces static propensity; surface resistivity on polyester yarn at 65% RH and 25°C measured per ASTM D257 falls to 10⁸-10¹¹ Ω. Overdosing above 8 wt% free acid lowers emulsion cloud point below 40°C and destabilizes the finish during high-speed splicing. The low titer of oleic acid, typically below 13°C per ISO 6321, allows pumpable liquid handling without heated storage, unlike stearic acid-based finishes.

    How Far Can High-Solids Alkyd Resin Solids Be Pushed With Oleic Acid-Linseed Oil Blends?

    High-solids alkyd resin syntheses use oleic acid as a monofunctional chain terminator. Oleic acid reduces weight-average molecular weight and lowers solution viscosity at 60% solids in xylene. In a medium-oil alkyd with oil length 55-65%, replacement of 10-30% of tall oil fatty acid by oleic acid is common. Reactor charge is heated under nitrogen to 230-250°C with xylene azeotropic removal. End point is acid value below 10 mg KOH/g per ASTM D974. Gardner viscosity at 60% solids is typically Z3-Z5. Film performance shifts when oleic acid exceeds 30% of fatty acid charge; Koenig pendulum hardness per ASTM D4366 declines, and through-dry time per ASTM D1640 lengthens. The oxidative crosslinking ability of the monoene chain is lower than linoleate-rich fatty acid mixtures. This creates a process boundary: production adjustments based solely on acid value cannot predict brush drag or open-time. Published data for this specific blended configuration is limited; plant batches frequently require gel permeation chromatography to confirm Mw and polydispersity before thinning to final solids. The acid value-viscosity curve flattens above 250°C; prolonged cook cycles increase dimer fatty acid formation and raise color beyond 6 Gardner.

    Sulfur-Cured SBR/NBR Compounds Demand Oleic Acid Purity Above 70%

    Because oleic acid lowers mill stickiness in NBR/SBR batches, it is used as a zinc oxide solubilizing co-activator in carbon-black-filled compounds. Addition of 1.0-3.0 phr oleic acid reduces stock adhesion at mill friction ratio 1:1.2. Mooney viscosity ML(1+4) 100°C measured per ASTM D1646 decreases by 5-15 MU when 1.5 phr oleic acid replaces the same mass of stearic acid. In moving die rheometer cure at 160°C and 0.5° arc per ASTM D5289, scorch time ts2 increases but final torque remains within ±10% of control. Tensile properties per ASTM D412 are maintained only if oleic acid acid value is below 200 mg KOH/g and iodine value is 85-95 g I2/100 g. Lower purity acid with saturated fraction above 5% causes processing aids to exude and reduces tack. At 3.0 phr, migration to mold surfaces becomes detectable as brown residue after 8 h of continuous press cycles at 160°C. In injection-molded nitrile rubber parts, clamp force settings above 150 t may cause bloom if oleic acid content exceeds 2.5 phr; this is more pronounced at mold temperatures below 160°C because acid solubility in the rubber matrix decreases. Mill batch temperature is often held below 70°C to prevent reaction with zinc oxide before curatives are added.In base-oil-based drilling fluids, calcium oleate soap formed in situ from oleic acid and excess lime stabilizes water-in-oil emulsion in paraffin-based systems. Continuous phase is diesel or low-aromatic mineral oil at 60-80 vol%. Internal phase is calcium chloride brine at 20-40 vol%. Oleic acid is added at 2-6 kg/m³ with emulsifier package. Electrical stability measured per API RP 13B-2 must remain above 500 V at 50°C. The soap film prevents coalescence under low-shear conditions at 3 rpm and 6 rpm Fann 35 viscometer readings. HPHT fluid loss at 150°C and 500 psi differential is controlled below 5 mL per API RP 13B-2. Excess lime above 5 lb/bbl converts free oleic acid to calcium oleate, raising plastic viscosity above 80 mPa·s and causing barite sag in inclined wellbores. Low shear yield point must stay above 5 lb/100 ft² to prevent barite settling over 16 h static aging at 150°C. Field mixing at 100-200 rpm on pit mud hoppers is preferred over direct brine contact. High-shear addition of oleic acid directly to brine can produce tight emulsions with 10-min gel strengths above 30 lb/100 ft², requiring dilution with base oil and additional emulsifier.

    When Oleamide From Oleic Acid Must Remain Below 0.3 wt% in LDPE Film

    Before extrusion, oleic acid is converted to oleamide via ammonolysis at 180-200°C over boric acid catalyst. In LDPE and LLDPE film, oleamide loading is typically 0.05-0.3 wt%. The polar amide group migrates to the film surface and reduces coefficient of friction. Dynamic coefficient of friction per ASTM D1894 on a stainless steel sled measured 24 h after extrusion falls from 0.45-0.55 to 0.15-0.25. At loadings above 0.3 wt%, chill-roll plate-out appears as a white haze on the cast film within 4-6 h of continuous running. Heat seal strength per ASTM F88 weakens because oleamide bloom contaminates the seal interface. Extruder barrel temperature must stay below 240°C to prevent amide dehydration to nitrile. For food-contact film, migration testing under EU Regulation 10/2011 is required; oleamide-specific migration data may be needed. Published migration data for high-temperature food simulants remains limited. Oleamide addition also reduces unwind noise and blocking; the required slip effect may take 24-48 h to fully develop after extrusion because migration is diffusion-controlled.For leave-on emulsions, oleic acid must be neutralized in situ with triethanolamine. The acid is used at 1.0-4.0 wt% of the oil phase. The resulting triethanolamine oleate has an HLB near 12, suitable for oil-in-water emulsion stabilization. Viscosity measured with a Brookfield RV viscometer spindle 4 at 20 rpm and 25°C typically reaches 8,000-15,000 mPa·s after 24 h storage. Peroxide value must remain below 5 meq/kg during accelerated aging at 40°C for 3 months. Cosmetic products containing oleic acid fall under Regulation (EC) No 1223/2009; oleic acid itself is not subject to Annex II or Annex III restrictions. Challenge testing per ISO 11930 is mandatory when water activity exceeds 0.6. Oleic acid is incompatible with cationic polymers such as polyquaternium-10; charge reversal causes immediate coalescence. Dermal sensitization risk is assessed with OECD 429; published data on leave-on use frequency is limited. Heat-stable emulsions require the oil phase to be maintained 10-15°C above the melting point of the oleic acid before neutralization to prevent acid droplets from crystallizing.

    Soluble Oil Metalworking Fluid Concentrates and Boundary Lubrication

    In soluble oil metalworking fluid concentrates, oleic acid operates both as an emulsifier and boundary lubricant. Oleic acid content in concentrate ranges from 5-22 wt%. Neutralization with triethanolamine or potassium hydroxide generates anionic soap. The concentrate diluted to 5% in water must produce a stable translucent-to-milky emulsion with particle size below 1.0 µm as measured by laser diffraction. Emulsion pH is maintained between 8.5-10.0. Four-ball wear scar per ASTM D4172 at 40 kgf, 1200 rpm, 60 min should remain below 0.60 mm. Low oleic acid levels produce hard water scum; high levels above 22 wt% cause heavy misting and dermatitis reports on production lines. Microbial growth is controlled by maintaining pH above 8.5 and adding biocide; dip-slide counts above 10⁵ CFU/mL per AFNOR NF T72-172 trigger shutdown. Oleic acid-derived soaps are sensitive to calcium and magnesium hardness; water hardness above 200 ppm CaCO₃ requires additional ethoxylated oleic acid co-emulsifier to prevent insoluble calcium oleate sludge.
    Concentrate parameterLow oleic acid formulationMid oleic acid formulationHigh oleic acid formulation
    Naphthenic base oil30-40 wt%20-30 wt%15-25 wt%
    Oleic acid5-8 wt%10-14 wt%18-22 wt%
    Triethanolamine3-5 wt%6-9 wt%10-13 wt%
    Petroleum sulfonate emulsifier8-12 wt%10-15 wt%12-15 wt%
    Waterbalancebalancebalance
    Emulsion pH at 5% dilution8.5-9.09.0-9.59.5-10.0
    Four-ball wear scar per ASTM D4172 at 40 kgf, 1200 rpm, 60 min≤0.70 mm≤0.60 mm≤0.50 mm
    Phosphate rock beneficiation uses oleic acid as an anionic collector for apatite. Conditioning is performed at pH 8-10 with sodium carbonate or sodium hydroxide as pH modifier. Collector dosage ranges from 0.2-0.8 kg/t of feed. Sodium silicate depressant at 0.5-1.0 kg/t controls quartz entrainment. A Denver D12 laboratory flotation cell at 1,500 rpm is the standard equipment for dose optimization. Recovery rises above 85% when collector dosage exceeds 0.4 kg/t, but concentrate grade falls below 30% P₂O₅ when dosage exceeds 0.6 kg/t because quartz and carbonate minerals float. Oleic acid adsorbs on apatite as chemisorbed calcium oleate; excess collector deposits as colloidal calcium oleate on bubble surfaces, destabilizing froth. Defoamer injection may then be required, and plant cell lip dimensions must be raised to prevent froth overflow. pH above 10.5 ionizes oleic acid fully but also causes slime swelling, reducing flotation kinetics.
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    Certification & Compliance
    More Introduction

    Oleic acid, systematically named cis-9-octadecenoic acid (CAS 112-80-1), is a monounsaturated C18 fatty acid with a single double bond at the C9–C10 position and a molecular mass of 282.461 g/mol. Commercial product is not a single molecular species but a fractionated fatty acid stream in which the nominal C18:1 content defines the grade. Standard industrial descriptors include 70%, 75%, 80%, 85%, 90%, and 95% oleic acid, with the balance composed primarily of linoleic, linolenic, stearic, palmitic, and minor C18 and C20 constituents. The source—tall oil, tallow, olive, rapeseed, or high-oleic sunflower—affects the ratio of unsaturated and saturated co-products and therefore governs viscosity, color, titer, and oxidative stability. At 25°C the material is typically a pale yellow to amber liquid or low-viscosity paste, and it remains readily pumpable in unheated stainless steel lines, whereas stearic acid requires heated storage above 55°C.

    How Is Oleic Acid Specified for Downstream Derivative Synthesis?

    Purchase specifications for oleic acid are organized around acid value, saponification value, iodine value, titer, moisture, and color. Acid value is the primary process variable in derivative manufacture because it fixes the stoichiometric consumption of alcohols, amines, and polyol hydroxyl groups. Iodine value is the critical differentiator for unsaturation-sensitive processes such as sulfation, ethoxylation, and hydrogenation. The following table presents representative industrial acceptance ranges for two common commercial forms.

    Parameter Technical grade High-purity grade Test method
    Nominal C18:1 content, wt% 70–75 90–98 GC, AOCS Ce 1-62
    Acid value, mg KOH/g 198–204 198–202 AOCS Cd 3d-63 / ISO 660:2020
    Saponification value, mg KOH/g 196–204 198–202 ISO 3657:2020
    Iodine value, g I2/100 g 85–100 85–95 AOCS Tg 1a-64 / ISO 3961:2018
    Titer, °C 8–15 4–10 AOCS Tr 1a-64
    Moisture, wt% ≤0.3 ≤0.05 ISO 662:2016
    Color, Lovibond 5¼ in ≤20Y/2R ≤5Y/0.5R AOCS Cc 13b-45

    Because high-purity grades from different botanical sources do not share a single titer profile, published data for this specific configuration is limited; buyers should request source-specific fatty acid methyl ester distribution rather than relying solely on nominal C18:1 content. In esterification plants, a batch-to-batch acid value shift of ±2 mg KOH/g alters the required alkali neutralization in downstream water-washing by up to 0.4 wt% sodium carbonate solution, which is significant when residual acidity must be held below 0.1 mg KOH/g.

    Across continuous methyl ester plants, oleic acid is blended with methanol at a molar ratio of 2.5:1 to 4:1 and esterified over an acidic ion-exchange resin or immobilized lipase. Reaction temperatures of 140–160°C under vacuum stripping at 20–50 mbar abs drive water removal and shift conversion; measured acid value is reduced to ≤1.0 mg KOH/g before the ester is neutralized. In batch ethoxylation, oleic acid is pre-dried to 0.02 wt% moisture and reacted with 2–20 mol ethylene oxide at 120–180°C using potassium hydroxide at 0.05–0.3 wt%; the residual acid value is typically terminated at ≤0.5 mg KOH/g. For amine-neutralized metalworking fluid additives, triethanolamine oleate is formed in jacketed stainless steel vessels at 75–95°C with anchor agitation until a clear concentrate is obtained; dilution pH at 5 wt% in deionized water is held between 8.0 and 9.5. These process windows are narrow because residual moisture above 0.2 wt% in the feedstock interferes with ethylene oxide insertion and increases side-product polyethylene glycol formation.

    In sulfochlorinated and sulfated derivative production, the monounsaturation of oleic acid permits controlled sulfation at the C9 double bond, but it also creates a heat-removal requirement not encountered with saturated lauric or stearic acid. Falling-film sulfonation reactors must maintain oleum or SO3 inlet temperatures of 40–50°C and cooling water at 20–30°C; local hot spots above 70°C darken the product and reduce active matter. Producers of quaternary fabric softeners first convert oleic acid to oleonitrile and then to oleyl amine; the final quaternization with methyl chloride is carried out under pressure in a stainless steel autoclave at 90–110°C until free amine content falls below 2.0 wt%. The narrower iodine value of high-purity grades reduces batch-to-batch variation in softener viscosity, which is otherwise observable as a spread of 80–120 mPa·s in 10% aqueous dispersions.

    When oleyl alcohol is the target derivative, oleic acid is hydrogenated over a copper-chromite catalyst at 250–300°C and 20–30 MPa hydrogen pressure in a trickle-bed reactor. Selective hydrogenation of the carboxyl group must preserve the C9 double bond when oleyl alcohol is desired; this requires the iodine value of the feedstock to remain within ±3 units of the nominal purchase specification because high linoleic co-content consumes hydrogen and raises saturated alcohol yield. The resulting oleyl alcohol typically retains an iodine value of 80–95 g I2/100 g and an acid value below 0.5 mg KOH/g, and it is further ethoxylated or sulfated for detergent and personal care intermediates.

    When Oleic Acid Replaces Stearic, Linoleic, or Erucic Acid in Formulation Development

    Selection among C18 fatty acids is determined by iodine value, titer, and chain-length effects on viscosity and oxidative stability. Oleic acid occupies an intermediate position between solid saturated stearic acid and highly unsaturated linoleic acid. The comparison table below summarizes the principal technical differences.

    Fatty acid Chain specification Iodine value, g I2/100 g Titer or melting point, °C Typical technical function
    Oleic acid C18:1 cis-9 85–95 8–15 liquid esters, lubricants, amine soaps
    Stearic acid C18:0 ≤2 54–57 rubber vulcanization activator, metal salts, PVC heat stabilizer
    Linoleic acid C18:2 cis-9,12 145–160 −5 to −8 alkyd drying resins, unsaturated chain extension
    Erucic acid C22:1 cis-13 65–75 33–34 slip agents, high-erucic oil derivatives

    These differences have direct processing consequences. A twin-screw compounding line that processes calcium stearate as a lubricant and acid scavenger cannot simply substitute oleic acid at equal loading without accounting for reduced melting point and increased unsaturation. In polyolefin extrusion, stearic acid at 0.05–0.20 phr acts as an external lubricant with a solid boundary layer, whereas oleic acid at the same addition level reduces viscosity more aggressively but can migrate to the die lip and form sticky deposits if barrel temperatures exceed 230°C. In alkyd resin synthesis, linoleic acid is selected for drying speed; oleic acid extends open time and yellowing resistance but requires a higher cobalt drier dose to achieve the same set-to-touch time. Published quantitative comparisons for this specific substitution are limited because commercial fatty acid blends vary in linoleic and linolenic co-content; the iodine value and peroxide value must be measured on each received lot rather than inferred from nominal grade.

    Storage in unheated carbon steel is generally acceptable for technical oleic acid, but high-purity cosmetic and pharmaceutical grades are transferred through 316L stainless steel or high-density polyethylene to prevent iron oleate formation. Tanks must be blanketed with nitrogen if shipment intervals exceed 30 days or if ambient storage temperature exceeds 35°C; peroxide values can rise above 10 meq/kg under repeated headspace air exposure, which invalidates subsequent sulfation and ethoxylation endpoints. Contact with copper, brass, cobalt, and manganese compounds accelerates oxidative degradation and should be restricted to components with <0.5 wt% copper alloy. Pre-drying at 80–95°C under 20–50 mbar abs is required for moisture-sensitive polyol ester and aluminum complex grease production, where water above 0.02 wt% causes batch turbidity and reduced thickener yield.

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