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| HS Code | 975422 |
| Chemical Name | Diethylene Glycol Monobutyl Ether |
| Cas Number | 112-34-5 |
| Molecular Formula | C8H18O3 |
| Molar Mass | 162.23 g/mol |
| Appearance | Colorless liquid |
| Odor | Mild, butyl-like ethereal odor |
| Density At 20 C | 0.955 g/cm³ |
| Boiling Point | 230°C |
| Melting Point | -68°C |
| Flash Point Closed Cup | 105°C |
| Autoignition Temperature | 365°C |
| Vapor Pressure At 20 C | 0.012 mmHg |
| Solubility In Water | Miscible |
| Viscosity At 25 C | 4.5 mPa·s |
| Refractive Index At 20 C | 1.4316 |
As an accredited Diethylene Glycol Monobutyl Ether factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Diethylene Glycol Monobutyl Ether packaged in 200 kg steel drums, securely sealed, labeled with product identification and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL: Diethylene Glycol Monobutyl Ether loaded in 200kg drums, secured with dunnage, labeled, and containerized safely. |
| Shipping | Diethylene Glycol Monobutyl Ether is shipped as a stable, non-hazardous liquid in drums, IBCs, or bulk tankers. Use clean, dry, dedicated equipment to prevent contamination. Keep containers tightly sealed, away from strong oxidizers and moisture. No special UN classification required under standard transport conditions, though proper labeling and documentation apply. |
| Storage | Store Diethylene Glycol Monobutyl Ether in tightly closed, properly labeled containers in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep separated from strong oxidizers, acids, and reactive chemicals. Ensure secondary containment to prevent spills. Avoid prolonged exposure to air and moisture. Inspect containers regularly for leaks or damage. |
| Shelf Life | Shelf life is typically 2–3 years when stored sealed, cool, dry, and away from oxidizers. |
Architectural waterborne latex paints based on acrylic, vinyl acrylic, and styrene-acrylic copolymer dispersions are formulated with diethylene glycol monobutyl ether (DEGBE) primarily as a coalescing solvent during the film formation phase. The solvent partition coefficient between the aqueous phase and polymer particle controls the depression of minimum film formation temperature (MFFT); DEGBE lowers MFFT in high-Tg acrylic lattices by displacing water from the particle-water interface and temporarily reducing the effective glass transition temperature of the coalescing binder. With a boiling point of 230 °C and a vapour pressure of 0.02 mmHg at 20 °C, DEGBE remains in the drying film through the continuous capillary deformation stage, then diffuses out at a rate governed by relative humidity and air velocity over the substrate. In interior wall paints formulated to EU Directive 2004/42/EC Phase II requirements, each addition increment must be checked against the ready-to-use VOC limit for interior matt wall and ceiling paints; in high-solids formulations with binder content above 45 wt%, a 3.0 wt% DEGBE addition can contribute approximately 30 g/L VOC depending on paint density, requiring reformulation with a softer latex or an extender. The typical addition ratio is 1.5–3.0 wt% of total wet paint formulation, or 5–12 wt% on binder solids depending on latex Tg. Production-scale high-speed dispersers with tip speeds between 15 m/s and 25 m/s incorporate DEGBE during the letdown stage after the pigment dispersion phase has cooled below 40 °C; addition before the grind phase can reduce dispersant efficiency by altering the solubility parameter of the aqueous phase and should be avoided where the dispersant is an ammonium salt of a low-molecular-weight polyacrylate. Finished products from this segment include interior wall paints, exterior masonry coatings, ceiling emulsions, and kitchen and bath paints; exterior grades formulated at 2.5–4.0 wt% DEGBE on total formula require accelerated weathering validation according to ASTM D4214-07 or ISO 16474-2:2013 before commercial release.
| Jurisdiction | Standard or Test Method | Scope | DEGBE-Related Control |
|---|---|---|---|
| European Union | 2004/42/EC, ISO 11890-2:2020 | Decorative paints and varnishes | Ready-to-use VOC content |
| United States | EPA Method 24, ASTM D2369-20 | Architectural and industrial maintenance coatings | Total volatile content minus water |
| China | GB 18582-2020, GB/T 23986-2009 | Architectural wall coatings | VOC, formaldehyde, heavy metals |
| International | ISO 11890-2:2020 | Paints and varnishes | Gas-chromatographic VOC determination |
Open time extension measured according to ASTM D7488-16 may require an addition ratio at the upper end of the window; however, in flat interior paints formulated to meet GB 18582-2020, the ratio must not exceed 3.0 wt% when the latex has a high free monomer content because residual solvent and monomer are co-determined by ISO 11890-2:2020. In production plants with ambient temperatures below 10 °C, coalescing efficiency of DEGBE declines unless the binder latex has been designed with a bimodal particle size distribution; film-cracking failures on low-temperature production lines have been traced to a Tg differential exceeding 12 °C between the coalesced binder phase and the crystalline pigment-extender interface. The proper control is a semi-continuous batch titration under ASTM D2354-10e1 with a MFFT bar gradient of 0–15 °C, because the solvent demand curve is non-linear above the coalescent saturation point.
In waterborne two-component polyurethane topcoats for agricultural and construction machinery, diethylene glycol monobutyl ether is introduced during the letdown stage rather than the pigment dispersion stage to prevent reaction with isocyanate hardeners at the dispersion interface. The addition window of 2.0–5.0 wt% of the total two-component formulation is selected according to the open time required during airless spray application at line speeds between 0.5 m/min and 1.8 m/min on large welded assemblies; the solvent decelerates the surface moisture release rate at ambient relative humidity values below 50%, thereby reducing dry spray and overspray adhesion loss on vertical steel sections. Industrial maintenance coating systems formulated to ISO 12944-5:2019 and tested under ISO 12944-6:2018 by neutral salt spray exposure of 720 h require that the DEGBE fraction not exceed 4.0 wt% where the primer contains zinc phosphate at a loading of 15–20 wt%; above this threshold, solvent retention in the cured film can increase water uptake in the first 24 h of immersion, degrading the electrochemical impedance modulus at 0.1 Hz. Production experience with 30:1 airless spray units fitted with 0.013–0.015 in reversible tungsten carbide tips indicates that batch-to-batch variation in DEGBE purity above 0.3 wt% water content produces sag on vertical substrates at fluid pressures above 170 bar; incoming solvent should be certified to a water content below 0.10 wt% and a peroxide value below 5 mg/kg. Adhesion retention after 720 h neutral salt spray is highly sensitive to residual DEGBE in the primer-topcoat interface; when a full topcoat contains 4.0 wt% DEGBE and force-drying is performed below 60 °C, the polyol-isocyanate reaction is not sufficiently complete before the solvent diffuses to the coating-air interface, causing blistering in a condensing humidity test according to ISO 6270-2:2017. Terminal finished products include two-coat polyurethane finishes on tractor chassis, crane booms, rail freight car interiors, and steel support structures for photovoltaic arrays.
Solvent balance in flexographic and rotogravure printing inks is adjusted to maintain ink transfer stability across press runs that exceed 100,000 linear metres on polyethylene and polypropylene films. Diethylene glycol monobutyl ether is used as a high-boiling glycol ether co-solvent at 5.0–12.0 wt% of the liquid flexo ink and at 3.0–8.0 wt% of the gravure letdown solvent blend, depending on the resin system; nitrocellulose-based flexo inks tolerate the upper band, while polyurethane-based lamination gravure inks require the lower band to avoid blocked ester curing during subsequent adhesive lamination. In flexographic printing, viscosity is controlled at 22–25 s on a Zahn 2 cup at 23 °C; DEGBE reduces the viscosity drift caused by evaporative loss of ethyl acetate and ethanol from the ink fountain, allowing the press operator to hold target viscosity for 20–30 min before automatic solvent replenishment is actuated. The solvent must be evaluated against Swiss Ordinance SR 817.023.21 for printing inks intended for food-contact packaging and against the European Union Good Manufacturing Practice Regulation 2023/2006/EC for food-contact material production; where the printed structure is used for confectionery or bakery overwrap, residual DEGBE in the dried ink film is measured by headspace gas chromatography following DIN EN 13628-1:2002, with the specification typically set below 50 mg/m² total residual solvent. Downstream production equipment includes central-impression flexographic presses with 8 or 10 colour stations running at 250–400 m/min, and gravure presses with engraved cylinder cell depths between 28 µm and 46 µm; the addition of DEGBE beyond 12 wt% can soften photopolymer plate materials below Shore A 55 after 4 h of continuous run time, causing dot gain in highlight areas above 3% halftone. Finished terminal products include surface-printed snack food wrappers, shrink sleeve labels, paper cups, wet-strength carrier bags, and reverse-printed lamination films for retort pouches.
At alkaline pH above 11.5, the coupling behaviour of diethylene glycol monobutyl ether in heavy-duty degreaser concentrates determines the phase stability window between concentrated alkali builders and nonionic surfactants with an HLB range of 10–13. The addition ratio in a ready-to-use spray degreaser is typically 1.0–5.0 wt%, while superconcentrates supplied for dilution at 1:40 may contain 4.0–8.0 wt% DEGBE; above 8.0 wt% the solvent can suppress the cloud point of alkyl polyglycoside blends below 5 °C, causing phase separation in unheated warehouses. Detergent products placed on the EU market must comply with Regulation (EC) No 648/2004 on detergent biodegradability and labelling, and mixtures must be classified under Regulation (EC) No 1272/2008 (CLP) for eye irritation and specific target organ toxicity after repeated exposure where DEGBE content exceeds the generic concentration limits. Batch mixing is performed in 1,000–5,000 L stainless steel vessels with low-shear axial impellers at 250–400 rpm; the addition sequence places DEGBE after the initial dilution of sodium hydroxide or potassium hydroxide to a final pH of 11.5–13.0, because direct contact between concentrated alkali and undiluted DEGBE can generate local temperature spikes above 60 °C and accelerate ether cleavage. Under no process condition should DEGBE be pre-blended with sodium hypochlorite at concentrations above 5 wt% available chlorine, as the combination generates heat and can degrade the glycol ether into chlorinated by-products; where a chlorinated degreaser is required, the glycol ether must be substituted with a non-oxidizable solvent. End-use equipment includes low-pressure foam guns, trigger sprayers, and immersion tanks operating at 40–60 °C; on stainless steel surfaces in meat processing rooms, the final rinse must achieve a conductivity below 20 µS/cm to avoid alkaline salt residue that can interfere with ATP hygiene monitoring. Terminal finished products include foaming oven and grill cleaners, self-cleaning floor degreasers for commercial kitchens, wheel and tire cleaners for vehicle detailing, and phosphate-free parts washer detergents for automotive remanufacturing lines.
Continuous rotary screen pigment printing of cellulose, polyester, and cotton-synthetic blends uses diethylene glycol monobutyl ether as a slow-evaporating solvent and plasticizer for the acrylic or butadiene-acrylic binder film in the aqueous print paste. Addition ratios of 10–30 g/kg of print paste are typical when the binder Tg exceeds 0 °C and the fixation oven length is limited to 8–12 m; the solvent retards skin-over of the print paste in the screen mesh during stop-and-start production cycles and reduces blade wear on rotary screens by maintaining paste viscosity between 12,000 mPa·s and 18,000 mPa·s at a shear rate of 1 s⁻¹. Textile auxiliaries and print pastes must be screened under the ZDHC Manufacturing Restricted Substances List v3.1 and, where applicable, the relevant appendices of OEKO-TEX Standard 100 for residues in finished fabric; DEGBE itself is not listed as a prohibited substance in ZDHC MRSL v3.1, but formulations containing it must still be declared under the facility chemical inventory and the final fabric must meet the volatile organic residue limits specified by the brand or buyer. The process is run on rotary screen printing machines with nickel screens of 80–125 mesh, a magnetic roll pressure of 3–6 mm, and drying in hot-air ovens at 130–150 °C for 2–4 min; lower fixation temperatures below 120 °C will retain DEGBE in the binder film and can reduce crock fastness measured under ISO 105-X12:2016 by half a grey scale rating. Finished goods from this application include pigment-printed jersey apparel, bed linen with pigment prints, upholstery fabrics, and polyester curtain panels; where the fabric is intended for children’s nightwear, the residual DEGBE content must be validated against flammability standards such as EN 14878:2007 or 16 CFR Part 1610 after the print is applied.
Unlike architectural latex systems, waterborne pressure-sensitive adhesive films are only partially coalesced at room temperature and depend on controlled solvent retention to achieve tack and peel performance. Diethylene glycol monobutyl ether is added at 1.5–3.0 wt% of the acrylic adhesive solids in the compounding vessel after the latex has been neutralized to pH 7.0–8.0 with ammonium hydroxide; this addition level plasticizes the acrylic polymer at the adhesive-substrate interface and permits coating onto silicone-coated release paper at line speeds of 20–50 m/min without micro-foaming in the drying tunnel. Adhesives intended for food-contact applications must satisfy FDA 21 CFR 175.105 for substances used in adhesives that may contact food through functional barriers, and EU REACH Annex XVII restrictions apply to any residual monomer or solvent migration above the specific migration limit assigned to the finished article. Production-scale coating uses comma bar or slot-die coaters followed by multi-zone air flotation dryers with zone temperatures of 60 °C, 80 °C, 100 °C, and 120 °C; because DEGBE has a relative evaporation rate of 0.004 compared with n-butyl acetate, the final 120 °C zone must be extended by 20–30% relative to a comparable formulation without DEGBE to reduce residual solvent below 1,000 mg/kg in the finished adhesive film. The terminal products include paper labels for beverage bottles, protective films for electronic touchscreens, double-sided tape backing adhesives, and freezer-grade packaging tapes; published data for the exact effect of DEGBE on loop tack as a function of drying zone residence time above 150 m/min is limited, requiring pilot-scale verification for each adhesive polymer grade.
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Diethylene Glycol Monobutyl Ether (2-(2-butoxyethoxy)ethanol, molecular formula C8H18O3, molar mass 162.23 g/mol) is supplied as a high-boiling glycol ether solvent under commercial designations including Butyl CARBITOL, Eastman DB Solvent, and generic technical-grade material. The CAS Registry Number is 112-34-5; the EINECS number is 203-961-6. The product is a clear, combustible liquid with a mild butyl odour, used primarily as a coalescent, coupling solvent, and slow-evaporating diluent in coatings, printing inks, and cleaning products.
At 20 °C the liquid density is approximately 0.953 g/cm³. The normal boiling point at 101.3 kPa is 230 °C. The closed-cup flash point determined by ASTM D93 is 100 °C. The vapour pressure at 20 °C is approximately 0.02 mmHg, which is roughly 1/40 of the vapour pressure of ethylene glycol monobutyl ether. The relative evaporation rate (n-butyl acetate = 1) is approximately 0.002.
For technical-grade material, the commercial specification is controlled by gas chromatography, Karl Fischer titration, and standard distillation and density methods. The acceptance window for water content is not a simple purity statement; it affects solvent activity in moisture-cure systems and should be confirmed when the material is used in urethane formulations. Table 1 lists the typical industrial specification.
| Property | Test method | Typical value or range |
|---|---|---|
| Assay by GC-FID | internal normalisation | ≥99.0 wt% |
| Water content | ASTM E203 | ≤0.10 wt% |
| Colour | ASTM D1209 | ≤10 Pt-Co |
| Density at 20 °C | ASTM D4052 | 0.952–0.955 g/cm³ |
| Distillation range | ASTM D1078 | 225–235 °C |
| Acidity as acetic acid | ASTM D1613 | ≤0.01 wt% |
| Refractive index at 20 °C | ASTM D1218 | 1.431–1.433 |
| Flash point, closed cup | ASTM D93 | 100 °C |
The material is hygroscopic; when water content must remain below 0.10 wt%, bulk storage in carbon steel tanks under dry nitrogen blanketing is specified. Vapour density relative to air is approximately 5.6, and the liquid pour point is below -60 °C, which permits handling in unheated transfer lines in most industrial settings. The octanol-water partition coefficient log Kow is approximately 0.56.
Addition of 2–5 wt% Diethylene Glycol Monobutyl Ether to a styrene-acrylic latex lowers the minimum film formation temperature measured under ASTM D2354; supplier technical data for styrene-acrylic binders report reductions of 4–8 °C at 3 wt% on polymer solids, although the exact response depends on particle size and surfactant coverage. The coalescing mechanism is plasticisation of the polymer-water interface, not permanent plasticisation. The solvent reduces the polymer phase glass transition temperature temporarily by increasing free volume and promoting interdiffusion of polymer chains across particle boundaries. Because the boiling point is 230 °C and the relative evaporation rate is approximately 0.002 (n-butyl acetate = 1), the solvent remains in the film long enough to bridge polymer particles across capillary pressure before diffusing to the surface and evaporating.
At application temperatures below 10 °C and relative humidity above 65%, coalescent demand increases; below 2 wt% the film may fail to form a continuous barrier, while above 5 wt% residual solvent can reduce block resistance measured by ASTM D4946 and lower Koenig pendulum hardness measured by ASTM D4366. Production-scale air-atomised spray equipment operating at 0.35–0.50 MPa fluid pressure and 1.5–2.0 m³/min air flow is used to apply these coatings; flash-off sections are typically set at 30–45 °C to remove water without trapping solvent under a prematurely dried surface. Film tack and hardness are monitored after forced-air drying at 23 °C and 50% relative humidity for 24 h.
Multi-station rotogravure and flexographic presses running above 150 m/min often blend Diethylene Glycol Monobutyl Ether at 2–6 wt% of total ink mass to extend open time on the cylinder and reduce drying of ink in the cells. Ink viscosity is monitored at press side with ISO 2431 flow cups; typical press-ready viscosity for flexible packaging inks falls between 18 s and 24 s at 25 °C. In solventless lamination, retained glycol ether can interfere with polyurethane adhesive bond development. Converters measuring residual solvent by headspace gas chromatography according to ASTM F2013 commonly set total residual solvent limits between 2 mg/m² and 5 mg/m² for high-coverage print areas. Diethylene Glycol Monobutyl Ether is therefore not used as the sole slow solvent at maximum press speeds; it is combined with ethyl acetate or methyl ethyl ketone to control drying while keeping retained high boiler below specification.
Oven drying profiles in such operations are set to raise web surface temperature to 55–70 °C in the final drying zone while maintaining air velocity above 20 m/s. The low vapour pressure of the material means that a wet ink film above 8 g/m² can retain measurable glycol ether even after 1.5 s residence in a drying hood. Published data for this specific high-coverage, high-speed configuration is limited; converter-specific trials using the actual press and dryer length are required before replacing a faster solvent with Diethylene Glycol Monobutyl Ether.
In high-speed bead mills using 0.5 mm yttria-stabilised zirconia beads, replacement of ethylene glycol monobutyl ether with Diethylene Glycol Monobutyl Ether reduces solvent evaporation from the open recirculation millbase. Nitrocellulose and polyurethane pigment concentrates achieve grind fineness below 10 µm on a Hegman gauge measured by ASTM D1210; millbase viscosity is maintained at 80–120 s by Ford cup according to ASTM D1200.
Hard-surface cleaner concentrates use Diethylene Glycol Monobutyl Ether at 3–10 wt% as a slow-evaporating coupling solvent, particularly where nonionic surfactants with pour points above 20 °C require solubility in alkaline builders. The amphiphilic structure—butyl endblock, internal ethylene oxide segments, and terminal hydroxyl—allows partitioning into hydrophobic oily soils while retaining aqueous rinseability. The material is compatible with sodium metasilicate and tetrapotassium pyrophosphate at pH 12.0 or lower; storage stability above pH 12.5 should be validated because glycol ethers can degrade under prolonged oxidising conditions. Ready-to-use trigger-spray degreasers contain 0.1–0.5 wt% solvent and rely on the material’s low vapour pressure to reduce odour and misting compared with ethylene glycol monobutyl ether. Heated immersion degreasing tanks at 45–55 °C show lower evaporative losses than shorter-chain glycol ethers, but exhaust ventilation must still be designed for heavier-than-air vapour.
The differentiation from shorter-chain glycol ethers is most visible in evaporation rate, vapour pressure, and water solubility. Table 2 compares typical values reported in supplier safety data sheets for Diethylene Glycol Monobutyl Ether and three related products.
| Parameter | Diethylene Glycol Monobutyl Ether | Ethylene Glycol Monobutyl Ether | Diethylene Glycol Monoethyl Ether | Propylene Glycol Monobutyl Ether |
|---|---|---|---|---|
| CAS Registry Number | 112-34-5 | 111-76-2 | 111-90-0 | 5131-66-8 |
| Molar mass | 162.23 g/mol | 118.17 g/mol | 134.17 g/mol | 132.20 g/mol |
| Boiling point at 101.3 kPa | 230 °C | 171 °C | 202 °C | 170 °C |
| Flash point, closed cup | 100 °C | 60 °C | 96 °C | 60 °C |
| Vapour pressure at 20 °C | 0.02 mmHg | 0.8 mmHg | 0.13 mmHg | 0.9 mmHg |
| Relative evaporation rate (n-butyl acetate = 1) | 0.002 | 0.079 | 0.01 | 0.08 |
| Viscosity at 25 °C | 5.3 mPa·s | 2.7 mPa·s | 4.3 mPa·s | 2.8 mPa·s |
| Water solubility | miscible | miscible | miscible | ~6 wt% at 20 °C |
Because Diethylene Glycol Monobutyl Ether is water-miscible while propylene glycol monobutyl ether is only partially water-soluble, clean-up and coupling behaviour differ in aqueous cleaner concentrates. The higher molar mass and lower vapour pressure of Diethylene Glycol Monobutyl Ether relative to ethylene glycol monobutyl ether reduce volatile emissions from open mixing tanks but also extend evaporation from dried films. This property is exploited in coatings and inks but becomes a constraint in high-speed packaging where residual solvent specifications are strict. The hydroxyl terminal group contributes to hydrogen bonding; theoretical hydroxyl number is approximately 346 mg KOH/g.
Strong oxidising agents and strong Lewis acids should be avoided at elevated temperatures because ether cleavage can occur. Bulk storage at ambient temperature in stainless steel or carbon steel with nitrogen blanketing is acceptable; copper and brass are generally avoided for long-term storage because trace metal ions can accelerate peroxide formation. Transfer piping and pumps should use stainless steel or chemical-resistant polymers such as polyethylene or fluoropolymer seals.