| HS Code | 602501 |
| Product Name | 2-Ethylhexyl Acetate |
| Abbreviation | 2EHA |
| Cas Registry Number | 103-09-3 |
| Einecs Number | 203-079-0 |
| Molecular Formula | C10H20O2 |
| Molecular Weight | 172.27 g/mol |
| Appearance | Colorless liquid |
| Odor | Mild fruity odor |
| Physical State | Liquid |
| Boiling Point | 199 °C |
| Melting Point | -80 °C |
| Density | 0.872 g/cm³ at 20 °C |
| Refractive Index | 1.4185 at 20 °C |
| Flash Point | 71 °C (closed cup) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble |
| Vapor Pressure | 0.1 mmHg at 20 °C |
| Logp Octanol Water | 3.72 |
| Autoignition Temperature | 260 °C |
| Viscosity | 1.2 mPa·s at 20 °C |
As an accredited 2-Ethylhexyl Acetate (2EHA) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Ethylhexyl Acetate (2EHA) supplied in 200 L steel drums, labeled hazardous, sealed, with proper chemical identification and safety markings. |
| Container Loading (20′ FCL) | 2-Ethylhexyl Acetate (2EHA) loaded in 20′ FCL containers, typically in 200L drums or IBCs, palletized, secured, and shipped. |
| Shipping | 2-Ethylhexyl Acetate (2EHA) is generally not regulated as dangerous goods for transport, though it is a combustible liquid. It is shipped in steel drums, IBCs, or ISO tanks. Store in cool, ventilated areas away from ignition sources and oxidizers. Ensure containers are sealed, labeled, and documented per local regulations. |
| Storage | Store 2-Ethylhexyl Acetate in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep containers tightly closed and upright in an approved, labeled, grounded flammable-liquid cabinet or storage room. Separate from strong oxidizers, acids, and bases. Avoid moisture. Use explosion-proof equipment and bonding/grounding during transfer. Observe local fire-code and chemical-storage regulations. |
| Shelf Life | Typically 24 months when stored sealed, cool, dry, well-ventilated, and away from heat, ignition, and moisture. |
In automotive refinish basecoat systems based on acrylic-polyol resins and cellulose acetate butyrate flow modifiers, 2-ethylhexyl acetate (CAS 103-09-3, boiling point 199 °C at 101.3 kPa, vapour pressure 0.03 mmHg at 20 °C) performs as a terminal tail solvent rather than a primary diluent. The material is introduced into solventborne basecoat concentrates at 3–8 wt% of the total formulation, with 1–4 wt% of Part A in 2K clearcoats, because its low vapour pressure keeps the wet film surface mobile during the 5–10 min flash-off window between the second basecoat pass and the clearcoat application. On vertical repair panels, addition below 3 wt% results in sag at wet film thicknesses above 25–30 µm, while addition above 8 wt% produces solvent popping in 2K clearcoats after forced drying with metal surface temperatures above 60 °C. The downstream process is spray application through gravity-feed HVLP guns with 1.2–1.4 mm nozzle sets and inlet air pressures of 2.0–2.5 bar, inside production spray booths with cross-flow velocities of 0.3–0.5 m/s and relative humidity 55–65%. In booths operating at the upper end of that RH range, batch-to-batch variation in 2EHA acid value above 0.05 mg KOH/g shifts sag resistance by approximately 10–15% because water absorption into the polyol part accelerates viscosity rise before the tail solvent can fully release; published data for this specific RH-dependent batch interaction is limited, and the observed shift derives from production batch records rather than a peer-reviewed test program. Compliance is governed by EU Directive 2004/42/EC Annex IIB for automotive refinish VOC limits and ASTM D2369-20 for VOC content determination; 2EHA is not VOC-exempt under 40 CFR 51.100(s) and must be counted in the organic solvent fraction. Terminal finished products include ready-to-spray basecoats, basecoat concentrates for automotive refinish tinting schemes, 2K polyurethane clearcoats, and primer surfacers for spot repair and whole-panel refinishing.
The transfer of a high-boiling acetate ester into a polyester-melamine coil coating line is constrained by one physical limit: the solvent must leave the film before the coating reaches the peak metal temperature where crosslinking begins and before the final cooling quench. 2EHA is incorporated at 2–6 wt% of total coating weight in high-solids polyester primers and topcoats with solids contents of 70–80% by mass; this is a narrow working window, not a convention, because below 2 wt% reverse-roller-applied films do not wet out 0.4 mm hot-dip galvanized steel surface roughness, and above 6 wt% residual solvent produces wave edges and a one- to two-grade reduction in pencil hardness from H to F or HB after cure. The downstream production process on a three-roll reverse roller coater with pick-up roll speeds of 120–140 m/min deposits wet films of 20–35 µm at line speeds of 60–150 m/min; the strip then passes through an air oven with first-zone air temperatures of 260–350 °C and a peak metal temperature of 216–232 °C for 20–40 s, measured by optical pyrometer at the exit of the final oven zone. Production data from lines running thin-gauge architectural coil show that when 2EHA loading exceeds 6 wt%, the residual ester plasticizes the melamine crosslink network and lowers the EN 13523-4:2022 pencil hardness result from H to HB, with the effect most pronounced on dark colours because higher pigment loading slows solvent diffusion. Compliance is governed by Directive 2010/75/EU BAT conclusions for surface treatment using organic solvents, ISO 11890-2:2020 for VOC content, and EN 13523-25:2022 for moisture and humidity resistance of coil-coated metals. Terminal finished product types include architectural cladding panels, domestic appliance side panels, garage door profiles, and pre-painted aluminium strip for roller shutter systems.
On multicolour flatbed and cylinder screen presses, the operational problem is not initial viscosity but the change in viscosity during press stops of 3–8 min; 2EHA is added at 5–15 wt% of total ink mass in solventborne screen inks based on acrylic or vinyl resin systems to keep the ink open on 120–165 threads/cm polyester meshes without dissolving the emulsion. Below 5 wt%, solvent inks clog mesh openings during short stoppages, and above 15 wt%, forced-air drying tunnels at 45–60 °C leave residual tack on printed stacks. The downstream process involves screen printing on flatbed or cylinder presses with squeegee hardness 75–80 Shore A, off-contact distance 1.5–2.0 mm, and interstation hot-air tunnels set at 45 °C for solvent release before the next colour is applied. In production on 12-colour carousel presses, batch-to-batch variation in 2EHA acid value above 0.05 mg KOH/g causes viscosity drift in aluminium-pigmented inks through acid-catalysed resin degradation, shifting dot gain by 2–4% on halftone graphic overlays; this is an observable process failure, not a theoretical risk. Compliance references include REACH Regulation (EC) No 1907/2006 Annex II, Regulation (EC) No 1935/2004 only where printed substrates are intended for food contact, and ISO 9001:2015 batch release controls; EN 71-3 is applicable only if the final printed article is classified as a toy. Terminal finished product types include membrane switches, graphic overlays, point-of-purchase displays, and industrial label stocks.
Within polyurethane hot-melt assembly adhesives, 2EHA is used as a controlled open-time extender rather than as the primary resin solvent. The typical addition is 1–5 wt% of the total adhesive formulation, pre-blended with a polyol resin component before the isocyanate curative is introduced; this extends open time from 10–15 min to 20–40 min at 25 °C and allows bead-applied assembly of automotive interior trim on variable-speed lines. The downstream production process uses a vacuum planetary disperser at 20–25 rpm for 30–45 min, followed by degassing at −0.09 MPa and application through precision dispensing needles with diameters of 0.3–0.6 mm; after bonding, the moisture-cure reaction of the isocyanate component displaces residual solvent during two-stage curing at 23 °C and 50% RH for 70–85 min. Operational limitations are explicit: addition above 5 wt% may lower initial lap shear strength at 24 h by more than 10% because residual 2EHA plasticizes the polyurethane matrix before the second cure stage; published data for this specific formulation configuration is limited, and the threshold is drawn from production batch comparison rather than a standardized interlaboratory study. Compliance is governed by REACH Regulation (EC) No 1907/2006 and ISO 11890-2:2020; food-contact use is not implied unless the final adhesive meets FDA 21 CFR 175.105 migration requirements for indirect food additives, with polymer-specific testing under 21 CFR 175.300 where applicable. Terminal finished product types include automotive interior structural adhesives, appliance trim bonding adhesives, and laminating adhesives for technical textiles.
Under cross-flow spray booth conditions with rotary atomizers operating at 25,000–40,000 rpm, a leather basecoat based on acrylic emulsion and polyurethane dispersion is applied at 15–30 µm dry film thickness; 2EHA is introduced at 2–6 wt% of the finish formulation as a coalescing tail solvent, and it slows skin-over on the atomizer bell and increases the levelling window to 20–40 s before the hide enters a drying tunnel at 50–80 °C. On production lines processing upholstery hides at 12–18 m/min, addition below 2 wt% produces spray-dried particle roughness on embossed grain surfaces, while addition above 6 wt% leaves residual tack after 24–48 h of block stacking because the solvent is retained in the polyurethane topcoat layer. The downstream process uses a rotary spray line with water-wash extraction and a three-zone convection tunnel; the finish is stack-pressed at 60–80 bar and 80–100 °C before final plated grain release. Compliance is governed by the ZDHC MRSL version 3.1 and REACH Regulation (EC) No 1907/2006; finish adhesion is tested by ISO 11644:2009 wet and dry rub fastness. Terminal finished product types include furniture upholstery leather, automotive interior leather, and technical leather for footwear uppers.
At 40 °C spray conditions, the viscosity response of high-solids maintenance topcoats is governed by the ester's low vapour pressure, which reduces viscosity without converting the solvent package into a fast-evaporating ketone blend that would dry-spray over large steel surfaces. 2EHA is used at 2–7 wt% of total formulation in acrylic-polyurethane and alkyd-urethane topcoats with volume solids of 65–80%; above 7 wt%, vertical I-beam webs airless-sprayed at 75–125 µm wet film thickness show sag development within 3–5 min after application, and below 2 wt% brush-applied touch-up areas exhibit pulling and loss of flow on warm steel. The downstream production process for steel fabricators uses airless spray equipment with reversible tips of 0.28–0.40 mm and fluid pressure 17.5–21.0 MPa, or plural-component spray systems with a 4:1 mix ratio and static mixers; the applied coating cures at ambient temperatures from 10 °C to 40 °C, and 2EHA extends the dust-free time to 60–90 min, which affects outdoor steel erection schedules. Compliance references include EPA 40 CFR Part 63 Subpart IIII for industrial maintenance coating VOC limits and ASTM D2369-20; corrosion protection performance is verified by ISO 12944-6:2018 and pull-off adhesion by ASTM D4541-22. Terminal finished product types include structural steel topcoats, storage tank exterior finishes, and process equipment enamels.
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2-Ethylhexyl acetate is a branched alkyl acetate ester with molecular formula C10H20O2, relative molecular mass 172.27 g/mol, and CAS registry number 103-09-3. It is produced by acid-catalysed esterification of 2-ethylhexanol with acetic acid, followed by fractionation to remove unreacted alcohol, water, and acid residues. Commercial product is supplied as a single technical ester grade; no separate ISO product model code is assigned. Supplier certificates of analysis for high-purity technical grade typically report ester purity ≥99.0%, density 0.870–0.874 g/cm³ at 20 °C, distillation range 198–205 °C, flash point 71 °C, water ≤0.05 wt%, acidity ≤0.02 mg KOH/g, and Pt-Co color ≤10. These are not universal specification limits; low-acid and low-2-ethylhexanol variants are specified when downstream chemistry is sensitive to active hydrogen or acid residues.
| Property | Typical acceptance range | Test designation |
|---|---|---|
| Ester purity | ≥99.0% | ASTM D3545 |
| Density at 20 °C | 0.870–0.874 g/cm³ | ASTM D4052 |
| Distillation range | 198–205 °C | ASTM D1078 |
| Flash point, closed cup | 71 °C | ASTM D56-05 |
| Water content | ≤0.05 wt% | ASTM E203 |
| Acidity as acetic acid | ≤0.02 mg KOH/g | ASTM D1613 |
| Pt-Co color | ≤10 | ASTM D1209 |
| Refractive index at 20 °C | 1.413–1.415 | ASTM D1218 |
The ester is differentiated primarily by evaporation rate, boiling range, and water partitioning. Relative evaporation rate is 0.01 with n-butyl acetate set at 1.0; n-butyl acetate boils at 126 °C and has a closed-cup flash point of 22 °C (ASTM D56), while propylene glycol monomethyl ether acetate boils at 146 °C, has a flash point of 45 °C (ASTM D56), and is fully water-miscible. 2EHA boils at 198–205 °C (ASTM D1078) and has a flash point of 71 °C (ASTM D56), with water solubility below 0.1 g/100 g at 20 °C. These differences do not alter total VOC content because 2EHA is not VOC-exempt; they shift the emission profile toward later oven stages. In coil coating ovens with peak metal surface temperatures of 210–232 °C, a 2EHA tail fraction can remain measurable by headspace gas chromatography at the oven exit if line speed exceeds 60 m/min, requiring verification by ISO 11890-2 or EPA Method 24 mass balance.
Because 2EHA is not fully water-miscible and has a branched aliphatic structure, it partitions differently in aqueous-organic systems than PGMEA. Its ester group is less aggressive toward some polar plastic substrates than methyl ethyl ketone but more hydrophobic than ethyl acetate, affecting ink adhesion on corona-treated polyethylene and polypropylene with wetting tension above 38 dyn/cm in ASTM D2578 evaluations. Selection against cyclohexanone or isophorone often depends on toxicological profile, flash point, and resin solution polarity rather than solvency alone.
| Property | 2-Ethylhexyl acetate | n-Butyl acetate | PGMEA | MIBK |
|---|---|---|---|---|
| Boiling point | 198–205 °C | 126 °C | 146 °C | 116 °C |
| Flash point, closed cup | 71 °C | 22 °C | 45 °C | 17 °C |
| Evaporation rate, n-Butyl acetate = 1 | 0.01 | 1.0 | 0.33 | 1.5 |
| Water solubility at 20 °C | <0.1 g/100 g | 0.7 g/100 g | miscible | 1.9 g/100 g |
| Density at 20 °C | 0.872 g/cm³ | 0.880 g/cm³ | 0.966 g/cm³ | 0.802 g/cm³ |
High-solids alkyd/melamine baking enamel lines use 2EHA as a tail solvent to reduce solvent boil, edge cratering, and particulate dewetting. Spray viscosity is commonly adjusted to 25–30 s Ford #4 cup at 25 °C (ASTM D1200), and 2EHA is added at 5–8 wt% of the total solvent phase. On rotary electrostatic bell equipment operating at 60–70 kV and 30,000–40,000 min⁻¹ atomizer speed, the slower solvent release reduces dry-spray droplets in high-humidity booths. The slow evaporation rate extends wet-edge time at 23 °C and 50% RH compared with butyl acetate-based control formulations, as evaluated by ASTM D1640 set-to-touch and ASTM D4400 sag-resistance methods. Excess addition above 12 wt% of total solvent can retain solvent in 40–50 µm dry films; if the oven profile does not exceed 150 °C peak metal surface temperature, residual solvent can survive bake and appear as soft film, blocking, or water sensitivity in stacked parts. Solvent pop in forced-air ovens becomes more likely when the transition from radiation to convection zones skins the film surface before evaporation. Oven profiling with data loggers at 10 °C increments is used to hold the solvent-release zone at 100–130 °C for 3–5 min.
Under cone-and-plate shear at 100 s⁻¹ (ISO 3219), a high-solids acrylic polyol at 75% nonvolatile content may show viscosity near 2,000 mPa·s at 25 °C. Addition of 2EHA at 3 wt%, 6 wt%, and 9 wt% of total formulation reduces viscosity to approximately 1,600 mPa·s, 1,100 mPa·s, and 760 mPa·s respectively; the system remains Newtonian over this range. For a solvent-borne epoxy base at 70% solids, 5 wt% 2EHA lowers initial mixed viscosity from 900 mPa·s to 520 mPa·s at 25 °C (ASTM D2196). These reductions are less pronounced than those from methyl ethyl ketone or butyl acetate on an equal-mass basis, but persist longer during open time due to the low evaporation rate. 2EHA is generally not used as the primary grinding solvent for pigment concentrates because its higher boiling point and viscosity reduce bead-mill efficiency; disperser tip speeds of 18–25 m/s require lower-viscosity co-solvents such as butyl acetate or methyl ethyl ketone. Published data for this specific high-solids formulation configuration are limited and should be replaced with resin-specific dilution curves.
In two-component aliphatic polyurethane topcoats, residual water, acidity, and low-molecular-weight hydroxyl species consume isocyanate crosslinker and disturb stoichiometry. For such use, a low-acid 2EHA variant is specified with acidity ≤0.01 mg KOH/g (ASTM D1613), water ≤0.03 wt% (ASTM E203), and 2-ethylhexanol content ≤0.05 wt% by GC (ASTM D3545). Receiving inspection should include retained-sample titration for water and acid because unsealed totes can absorb moisture above 0.15 wt% within 48 h at 25 °C and 80% RH. Nitrogen blanketing or sealed drying-tube vents are used to exclude atmospheric moisture. If pre-blended with aromatic solvent and stored in carbon steel, trace iron may rise; filtered samples should be checked by ICP-OES according to ASTM D5185 when metal-sensitive clearcoats are produced. Amine-based moisture scavengers should not be combined with 2EHA without verification of ester-amine interaction because transesterification or amide formation is possible at elevated storage temperatures above 40 °C.
Long-term hydrolytic stability is limited outside neutral pH. Hydrolysis to 2-ethylhexanol and acetic acid becomes significant in aqueous media below pH 3 or above pH 11 at temperatures above 50 °C. In immersion tests based on ASTM D1308, residual acetic acid from unflashed 2EHA can etch aluminum substrates or reduce adhesion of amine-cured epoxy layers. Published data for continuous aqueous service of 2EHA in industrial cleaning formulations are limited; cleaner concentrates should be tested at the exact pH and temperature boundaries of the intended line, not inferred from ambient solvency data.
Vapor pressure at 20 °C is approximately 0.02 kPa; heated cleaning baths at 60–80 °C elevate saturation vapor concentration and require mechanical ventilation. Since no ACGIH TLV or OSHA PEL is established specifically for 2EHA, exposure control is typically based on process saturation calculations and local exhaust ventilation rates of 10–20 air changes per hour. The material has a closed-cup flash point of 71 °C (ASTM D56) and is classified as a combustible liquid under GHS category 4; open transfer near ignition sources above flash point should be avoided. Thermal degradation in air can begin above 150 °C and yield acetic acid, carbon monoxide, and short-chain aldehydes. Published data for this specific degradation pathway are limited, so oven afterburner and acid-gas scrubber design must account for ester decomposition products.
In flexographic and gravure printing inks, 2EHA serves as a slow ester solvent in nitrocellulose and polyamide resin systems. Ink viscosity is often held at 18–22 s using a 3 mm ISO cup (ISO 2431) at printing press speeds of 150–250 m/min; 2EHA content of 2–5 wt% can reduce surface defects without blocking in fast-drying tunnels. Above 7 wt%, blocked rewinds and ink transfer defects may appear because the solvent remains in the printed film longer. Its low water solubility of <0.1 g/100 g at 20 °C reduces moisture blush in humid print rooms compared with fully water-miscible glycol ether acetates.