Gum Rosin

    • Product Name: Gum Rosin
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code
    Product Name Gum Rosin
    Cas Number 8050-09-7
    Einecs Number 232-475-7
    Appearance Translucent solid
    Color Pale yellow to reddish brown
    Form Lumps, flakes, or powder
    Odor Faint turpentine-like odor
    Softening Point 70-80 °C
    Melting Point 100-140 °C
    Acid Value 160-180 mg KOH/g
    Saponification Value 170-190 mg KOH/g
    Density 1.07-1.09 g/cm³ at 20 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in alcohol, ether, benzene, chloroform, and turpentine
    Flash Point >180 °C
    Boiling Point >300 °C
    Refractive Index 1.545 at 20 °C
    Main Components Abietic acid, pimaric acid, and other resin acids
    Source Pine tree exudate (Pinus species)
    Hazard Class Combustible solid; may cause skin sensitization
    Storage Conditions Cool, dry, well-ventilated area

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

    Packing & Storage
    Packing Gum Rosin is packaged in 25 kg net multiwall paper bags, palletized and shrink-wrapped for safe industrial transport and storage.
    Container Loading (20′ FCL) 20′ FCL loading: Gum Rosin packed in 80 galvanized iron drums, 225 kg net each, total 18 MT, securely stowed.
    Shipping Gum Rosin is normally shipped as non-regulated general cargo in lined drums, bags, or cartons. Store in a cool, dry, well-ventilated area away from ignition sources and moisture. Although not generally classified as dangerous goods, handle as a combustible solid and comply with local transport rules.
    Storage Store Gum Rosin in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep containers tightly closed when not in use. Protect from moisture and contamination. Separate from strong oxidizers, acids, and alkalis. Use grounded equipment to prevent static buildup. Avoid dust generation. Follow local fire codes and maintain appropriate firefighting equipment.
    Shelf Life Gum rosin shelf life is about two years if stored sealed, cool, dry, and protected from heat, light, and moisture.
    Application of Gum Rosin

    Rosin ester–EVA hot melt systems: slot-die run speeds and open-time limits

    Gum rosin is converted to glycerol or pentaerythritol esters before being compounded into ethylene-vinyl acetate hot-melt adhesives at loadings of 25–40 wt% relative to total formulation mass. Glycerol esters selected for lower melt viscosity have ring-and-ball softening points of 82–96 °C; pentaerythritol esters with softening points of 95–108 °C are chosen when the adhesive must withstand shear adhesion failure temperatures above 65 °C under ASTM D4498. Finished adhesive melt viscosity at 180 °C is measured by ASTM D3236 and is typically held between 0.8 Pa·s and 6.0 Pa·s. In corrugated case sealing and rotary labelling, open time is maintained at 1.5–2.5 s while set time under compression is kept below 0.8 s; these demands are balanced by co-formulating fully hydrogenated paraffin wax at 15–25 wt% and an antioxidant package at 0.1–0.5 wt%. Loadings below 20 wt% produce insufficient wetting on recycled kraft linerboard, resulting in fiber tear below 80%, whereas loadings above 50 wt% reduce cohesive strength and cause low-temperature cracking at −10 °C in EVA grades containing less than 18 wt% vinyl acetate. Compounding takes place in a jacketed sigma-blade mixer with a working volume of 200–2,000 L at 160–180 °C under nitrogen sweep, followed by vacuum devolatilization at −0.09 MPa for 20–40 min; slot-die application temperature is maintained at 150–175 °C. Residual acid numbers above 12 mg KOH/g are avoided in continuous production because free abietic acid accelerates corrosion of carbon steel melters and produces viscosity drift across shifts. For food-contact packaging, FDA 21 CFR 175.105 covers rosin-based hot-melt adhesives, and EU Regulation 10/2011 migration testing is added when the adhesive is used in direct food-contact packaging. Terminal products include corrugated case sealing, rotary beverage labelling, bookbinding, and disposable hygiene assembly.

    For sheetfed and heatset web offset printing, gum rosin is converted into a rosin-modified phenolic resin by reacting with p-tert-butylphenol-formaldehyde condensate at 180–220 °C and then esterifying with pentaerythritol at 230–250 °C. The final varnish contains 30–45 wt% rosin-modified resin solids; the finished ink contains 15–25 wt% of this resin. Gelation with aluminium 2-ethylhexanoate at 0.2–0.8 wt% on varnish solids is used to adjust viscoelasticity and misting behavior; Laray viscometry at 25 °C and 2,500 s−1 is used to control tack. Low-migration inks for food packaging are evaluated for colorimetric conformance under ISO 2846-2:2015, for migration under EU Regulation 10/2011 and EC 1935/2004, and for restricted components under the EuPIA Exclusion Policy. Production is carried out by pre-dispersing the pigment and varnish in a twin-screw extruder at barrel temperatures of 80–110 °C, followed by three-roll milling to a grindometer fineness below 5 µm. Heatset web offset inks formulated with these resins tolerate press speeds of 1,200–1,500 m/min without misting, provided the resin acid number is below 20 mg KOH/g. Terminal products are low-migration folding carton inks, sheetfed commercial print inks, and heatset web publication inks.

    Can rosin soap control emulsion SBR latex particle size below 150 nm?

    In cold emulsion styrene-butadiene rubber production, disproportionated gum rosin is saponified with potassium hydroxide to form a mixed rosin/fatty acid soap at 2.0–5.0 phr per 100 parts of styrene and butadiene monomer. The soap is added continuously to a stirred reactor train maintained at 5–8 °C; a ferrous-formaldehyde sulfoxylate redox initiator system drives polymerization, and shortstop is injected at 60–65 wt% monomer conversion to suppress gel formation. Latex particle size is regulated by soap concentration and agitation power; dynamic light scattering measurements typically yield a mean diameter of 80–130 nm with a polydispersity index below 0.08. Rosin soap contributes to mechanical stability and reduces pre-coagulum in continuous reactors, but batch-to-batch variation in abietic acid content above 70 wt% is associated with latex viscosity drift and fouling of heat exchanger surfaces. After shortstop, unreacted butadiene is removed by steam stripping, and the latex is coagulated with sulfuric acid and sodium chloride, washed, dewatered, and dried in an apron dryer. Raw rosin used in SBR production is evaluated against ISO 2322:2019 for SBR evaluation; colophony skin-sensitization classification under EU Regulation 1272/2008 Annex VI requires operation under local exhaust ventilation and closed transfer. Terminal products include tyre tread compounds, conveyor belt covers, footwear soles, and moulded rubber goods.

    In wave and reflow soldering of printed circuit board assemblies, purified gum rosin is dissolved in isopropyl alcohol or ethanol at solids loadings of 15–45 wt% for rosin-based liquid fluxes; no-clean formulations reduce rosin content to 1–5 wt% and use succinic acid or glutaric acid activators at 0.5–2.0 wt%. The rosin functions as a thermally activated fluxing vehicle and oxidation barrier; its acid number before thermal exposure is typically 160–170 mg KOH/g. Preheat is set to 90–130 °C for 60–90 s, and reflow peak temperature for SAC305 solder paste is 240–250 °C; wave soldering pot temperature is maintained at 255–265 °C. Surface insulation resistance is evaluated by IPC-TM-650 2.6.3.7 at 85 °C/85% RH with a pass threshold of 100 MΩ. Heavy rosin residues from wave soldering are removed with saponified aqueous cleaners; cleanliness is checked by ROSE testing per IPC-TM-650 2.3.25 against a threshold of 1.56 µg/cm² NaCl equivalence. Flux activity classification follows IPC J-STD-004C, and the final assembly must satisfy RoHS Directive 2011/65/EU for lead-free solder compatibility. Terminal products are automotive electronic control units, consumer electronics, power supply boards, and industrial control assemblies.

    Application segmentMandatory referenceTest method designationControl parameter
    Hot-melt adhesivesFDA 21 CFR 175.105, EU Regulation 10/2011ASTM D3236, ASTM D4498Melt viscosity at 180 °C, shear adhesion failure temperature
    Offset printing inksISO 2846-2:2015, EC 1935/2004Laray viscometry, grindometerTack at 2,500 s−1, fineness below 5 µm
    Emulsion SBRISO 2322:2019, EU Regulation 1272/2008Dynamic light scatteringLatex particle size 80–130 nm, conversion 60–65 wt%
    Soldering fluxIPC J-STD-004C, RoHS Directive 2011/65/EUIPC-TM-650 2.6.3.7, IPC-TM-650 2.3.25Surface insulation resistance 100 MΩ, ionic contamination 1.56 µg/cm²
    Paper sizingFDA 21 CFR 176.170ISO 535, TAPPI T 261Cobb water absorption 20–30 g/m², first-pass retention
    Chewing gum baseFDA 21 CFR 172.615, INS 445Acid number, softening pointAcid number below 8 mg KOH/g, residual abietic acid below 1 wt%
    Alkyd coatingsDirective 2004/42/ECASTM D2369, grindometerVOC content, fineness below 30 µm

    Paper sizing deposits and aluminum sulfate interactions at pH 4.5–6.0

    Gum rosin is saponified with sodium hydroxide to produce sodium rosinate with 70–85 wt% solids and pH 9.5–11.0; this rosin size is added to thin stock at 0.2–1.2 wt% based on oven-dry fibre. Aluminium sulfate is then introduced to reduce the headbox pH to 4.5–6.0 and to precipitate aluminium resinate onto the fibre surface. Cationic starch at 0.5–1.5 wt% is used to control zeta potential and first-pass retention; retention is monitored by TAPPI T 261, and sized linerboard is evaluated by ISO 535 Cobb testing with values typically 20–30 g/m² at 60 s contact. Multi-cylinder dryer sections operate at 80–120 °C to cure the rosin-alum complex and reduce rewetting. For food-contact paper and paperboard, FDA 21 CFR 176.170 permits rosin size; REACH compliance for sodium rosinate in EU markets is managed through the registration dossier. Terminal products include corrugated medium, gypsum board facing, folding boxboard, and printing/writing paper.

    When gum rosin esters replace synthetic elastomers in chewing gum base

    Food-grade gum rosin is esterified with glycerol or pentaerythritol and then hydrogenated to reduce residual abietic acid to less than 1 wt%; the resulting rosin ester has an acid number below 8 mg KOH/g and a ring-and-ball softening point of 80–90 °C. In gum base compounding, the rosin ester is blended with food-grade polyvinyl acetate, microcrystalline wax, and talc in a Z-blade mixer at 110–120 °C; rosin ester dosage is 5–15 wt% of the gum base. The cooled gum base is mixed with sorbitol, xylitol, flavouring, and encapsulated sweeteners at 45–55 °C to limit flavour loss and thermal degradation. Compliance is governed by FDA 21 CFR 172.615 and the JECFA monograph for glycerol ester of gum rosin (INS 445); European purchasers also verify heavy metal limits and residual solvent specifications through the EU food additive framework. Acid numbers above 8 mg KOH/g are associated with bitterness and oxidative rancidity, limiting shelf life. Terminal products are chewing gum pellets, sticks, and coated tablets.

    In solvent-borne alkyd coatings for traffic marking and anticorrosive primers, gum rosin is cooked into the alkyd resin at 5–15 wt% of total resin solids. The rosin is added with pentaerythritol and a calcium or lithium catalyst at 230–250 °C, and the cook is continued until the acid number falls below 15 mg KOH/g. Replacing part of the linseed oil or soybean oil fatty acid with rosin raises glass transition temperature and shortens dust-free time to 15–25 min at 25 °C and 50% RH. Final solvent-borne traffic paints are supplied at 45–55 wt% non-volatile solids. Compliance for volatile organic content is tested by ASTM D2369, and EU products must respect the relevant subcategory limits in Directive 2004/42/EC. Production is completed in a high-speed disperser followed by a bead mill at 40–50 °C; fineness of grind is held below 30 µm. Rosin addition above 20 wt% induces yellowing and embrittlement, making it unsuitable for white or light-coloured exterior finishes. Terminal products are road marking paints, anticorrosive primers, and quick-dry enamels.

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    Certification & Compliance
    More Introduction

    Gum rosin is the non-volatile diterpene acid fraction recovered by steam distillation of pine oleoresin tapped from living Pinus species, principally Pinus massoniana, Pinus elliottii, and Pinus pinaster. The product is a pale yellow to dark amber glassy solid with CAS registry number 8050-09-7 and EINECS 232-475-7. Commercial identity is defined by USDA color grades X, WW, WG, N, M, and K; WW and WG are typical release grades for tackifier synthesis, while K is reserved for darker, higher-colour streams. The grade encodes a colour boundary, acid number band, and softening point range rather than a single model code. The material is a multicomponent diterpene acid mixture in which abietane-type resin acids dominate over pimarane-type acids. Published compositional surveys of Pinus massoniana gum rosin report abietic, neoabietic, palustric, levopimaric, dehydroabietic, pimaric, isopimaric, and sandaracopimaric acids as the principal resolved peaks.

    The primary industrial function of gum rosin is as an acid-functional tackifier and as the esterification feedstock for rosin ester resins. In hot-melt adhesive compounding, free-acid gum rosin is frequently converted to pentaerythritol or glycerol esters before formulation because the high acid number can generate viscosity instability and equipment corrosion. In solder flux and rubber processing, free-acid gum rosin retains direct use. The polar carboxylic acid group provides adhesion to metal oxides and cellulosic substrates, while the fused-ring diterpene framework contributes compatibility with low-polarity polymer phases. Compared with C5 and C9 petroleum hydrocarbon resins, gum rosin has a much higher acid number and a lower weight-average molecular weight, typically below 400 g/mol, whereas hydrocarbon resins are nonpolar and oligomeric. This distinction governs selection in polar substrate bonding and in esterification; hydrocarbon resins cannot be esterified with polyols to form high-softening-point tackifiers.

    What Differentiates Gum Rosin from Tall Oil Rosin and Wood Rosin at the Process Level?

    Source and isolation route create measurable differences in unsaponifiable matter, sulfur residue, and initial colour. Gum rosin is recovered from live-tree oleoresin; tall oil rosin is a co-product of kraft pulping and requires acidulation of black liquor soap skimmings; wood rosin is obtained by solvent extraction of aged pine stumps. Tall oil rosin retains sulfur-bearing malodour compounds and can exhibit wider batch-to-batch variation in colour because black liquor composition tracks wood furnish and pulping liquor cycles. Wood rosin typically contains higher oxidised diterpene content from prolonged stump weathering and may require hydrogenation or disproportionation to stabilise colour. Commercial gum rosin is typically selected for lower unsaponifiable matter and lighter initial colour, which reduces downstream purification demand in esterification. These distinctions are observed in routine release testing rather than in polymer end-use tensile data, where formulation variables obscure raw-resin differences.

    Specification release for commercial WW grade is controlled primarily by colour, acid number, softening point, unsaponifiable matter, and ash. The table below lists conventional release windows reported for gum rosin intended for esterification in adhesives; limits should be confirmed with the supplier because tapping season and pine species shift the diterpene acid profile.

    ParameterMethodTypical release window
    USDA colour gradeASTM D509-15WW or WG
    Acid numberASTM D465-15165–175 mg KOH/g
    Softening pointASTM E28-1876–82 °C
    Unsaponifiable matterASTM D1065-18≤5.0 wt%
    AshASTM D1063-18≤0.02 wt%

    Acid number is the most sensitive incoming inspection parameter for esterification because it determines the stoichiometric pentaerythritol or glycerol charge. A batch-to-batch acid number variation of ±3 mg KOH/g can shift hydroxyl conversion and alter final ester softening point. Softening point is measured on a ball-and-ring apparatus and is used to detect contamination from wood rosin or oxidised recycled streams, which tend to raise the measured value without increasing tackifier performance.

    When Pentaerythritol Esters Replace Free-Acid Gum Rosin in Hot-Melt Tackification

    Esterification with pentaerythritol or glycerol consumes the resin acid carboxylic acid group and converts a high-acid, low-softening-point intermediate into a low-acid, higher-softening-point tackifier. For gum rosin, pentaerythritol ester grades typically exhibit acid number below 15 mg KOH/g, softening point from 94 °C to 106 °C, and colour controlled by esterification catalyst and inert-gas sparge. These esters are added to styrene-isoprene-styrene and styrene-butadiene-styrene hot-melt pressure-sensitive adhesives at concentrations from 30 wt% to 60 wt%. They shift the midblock glass transition temperature and modify the loss tangent at service temperature; compatibility is commonly evaluated by dynamic mechanical thermal analysis and by cloud point after accelerated storage at 60 °C. Free-acid gum rosin differs from its esters principally in acid number, melt viscosity, and oxidative stability; the free acid is not a direct substitute for a pentaerythritol ester in a formulation designed around a softening point above 90 °C.

    On production-scale hot-melt compounding lines, free-acid gum rosin is pre-melted in agitated stainless steel vessels and metered by gear pump. High-shear dispersion is not required for the rosin itself because it is a low-molecular-weight melt; shear is applied when the rosin is combined with high-viscosity elastomer phases. Moisture above 0.2 wt% promotes foaming during high-temperature esterification; pre-drying at 80–90 °C under vacuum is used when storage RH exceeds 60%. Amine-based additives should be avoided in free-acid rosin systems because carboxylate salt formation may increase melt viscosity and reduce tack. In semi-crystalline polyolefin matrices, the polar rosin acid phase can migrate to the surface because compatibility declines as crystallinity increases; quantitative compatibility should be measured by cloud point and exudation after ageing at 60 °C. Published data for this specific configuration is limited.

    Thermal Dimerization and Antioxidant Response in Rosin Acid Isomerization

    Unmodified gum rosin is thermally sensitive because conjugated double bonds in abietane-type acids are susceptible to isomerisation and oxidation above 120 °C. Industrial esterification therefore uses inert-gas blanketing, phosphite or phenolic antioxidants, and controlled heating rates. Thermal treatment produces dehydroabietic acid and dimeric species; the latter raise melt viscosity and can reduce tackifier solubility in aliphatic elastomer phases. Differential scanning calorimetry of commercial gum rosin typically shows a glass transition in the range of 30–45 °C and a broad oxidative exotherm beginning above 130 °C when scanned in air at 10 K/min, though published data for this specific configuration is limited. The operational boundary is therefore strict: prolonged melt hold time above 120 °C without antioxidant protection accelerates colour development and increases dimer content, changing the acid number and softening point of the residual free rosin.

    Free-acid gum rosin is directly used in rosin-based solder flux where the carboxylic acid function activates oxide removal at soldering temperatures. Flux classification follows IPC J-STD-004; rosin fluxes are designated RO with an activity level and halide index, typically RO L0 or RO M0 for no-clean and standard rosin-activated systems. In rubber compounding, gum rosin functions as a dispersing agent and processing tackifier at loadings below 3 phr in many tyre tread formulations; higher loadings may retard sulphur cure. The acid number limits zinc-oxide activity in halobutyl rubber compounds; pilot-mixer evaluation is required before line-scale substitution.

    REACH Registration Does Not Eliminate Downstream Use Verification

    For indirect food-contact adhesive applications, gum rosin and rosin derivatives may be evaluated under 21 CFR 175.105 and 21 CFR 175.125, provided the finished adhesive meets migration limits and functional barrier requirements. Not every rosin grade qualifies; food-contact use requires supplier confirmation of purity criteria under the applicable regulation. REACH registration status for CAS 8050-09-7 must be verified for the European market because the substance is considered a natural complex substance, and downstream users must disclose identified uses to the registrant. RoHS directives do not list rosin as a restricted substance; however, heavy-metal screening for lead, cadmium, mercury, and hexavalent chromium is advisable for electrical flux grades and electronics assembly operations.

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