| HS Code | 638862 |
| Productname | Lithol Rubine 8B |
| Colorindexname | Pigment Red 57:1 |
| Colorindexnumber | C.I. 15850:1 |
| Casnumber | 7582-28-7 |
| Chemicalclass | Monoazo calcium lake |
| Appearance | Red powder |
| Colorshade | Bluish red |
| Specificgravity | 1.80-1.90 |
| Oilabsorption | 45-55 g/100g |
| Ph | 7-8 |
| Moisturecontent | ≤1.5% |
| Watersolubility | Insoluble |
| Lightfastness | 4-5 (blue wool scale) |
| Heatresistance | 180-200 °C |
| Acidresistance | Good |
| Alkaliresistance | Fair |
| Migrationresistance | Good |
As an accredited Lithol Rubine 8B factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Lithol Rubine 8B is supplied in 25 kg moisture-resistant paper bags with inner polyethylene liners, palletized for industrial handling. |
| Container Loading (20′ FCL) | Lithol Rubine 8B pigment is loaded into a 20-foot FCL container, palletized and secured for dry, compliant ocean shipment. |
| Shipping | Lithol Rubine 8B (CI Pigment Red 57:1) is shipped as a non-hazardous powder in sealed, polyethylene-lined bags or fiber drums. Transport in cool, dry conditions, protected from moisture, heat, and direct sunlight. It is not classified as dangerous goods for transport. |
| Storage | Store Lithol Rubine 8B in a cool, dry, well-ventilated warehouse away from direct sunlight, heat, ignition sources, and incompatible oxidizers. Keep containers tightly closed, labeled, and in original packaging, palletized off the floor and protected from moisture. Prevent dust generation and accumulation; use local exhaust, good housekeeping, and follow the supplier’s SDS and local regulations. Do not store near food or feed. |
| Shelf Life | Lithol Rubine 8B is stable under normal storage conditions; protect from moisture, heat, and light, with a typical shelf life of 24–36 months. |
In aqueous flexographic printing of paper-based packaging, Lithol Rubine 8B (C.I. Pigment Red 57:1) is introduced as a 35 wt% pigment concentrate milled in an alkali-soluble styrene-acrylic resin solution, then reduced to 10–12 wt% pigment in the press-ready ink. The downstream production sequence starts with a rotor-stator high-shear disperser operating at 15–20 m/s peripheral speed, followed by a horizontal bead mill charged with 0.8–1.2 mm yttria-stabilized zirconia media; grinding continues until fineness on an ISO 1524:2013 gauge remains below 5 µm. Production-scale batches are observed to drift in colour strength when the letdown vehicle pH rises above 8.6 because the calcium lake undergoes progressive deagglomeration and soluble calcium release; the vehicle is therefore buffered to 8.2–8.5 with low-amine neutralisers. Regulatory compliance for paper carrier bags, napkins, tissue wraps, and gift wrap normally requires REACH Regulation (EC) No 1907/2006 and the EuPIA Suitability List for printing inks on non-food-contact paper and board; direct food-contact clearance under Regulation (EC) No 1935/2004 or FDA 21 CFR 175.300 must be demonstrated through end-user migration testing, not assumed from pigment data alone. Terminal articles printed at 150–250 m/min contain a magenta shade that retains sufficient water fastness for converter-level handling; exposure to alkaline soap solutions above pH 10 may extract surface calcium and should be avoided in wet-wipe paper packaging unless an overprint varnish is applied.
The calcium lake’s interaction with low-viscosity mineral oil in sheet-fed offset vehicles creates a specific failure pathway when free calcium ions migrate into the fountain solution and redeposit on the water train as tinting contamination. The typical addition ratio for high-strength rubine spot colours is 16–20 wt% based on finished ink mass; flushed pigment dispersions are preferred over dry powder because they reduce dust exposure and eliminate the first-pass deagglomeration step on the mill. Downstream production uses a hydraulic three-roll mill with chilled rolls maintained at 30–40°C and nip pressure set to deliver a fineness below 10 µm according to ISO 1524:2013. Press-ready ink tack is measured by ASTM D4361:2010 on an Inkometer at 32°C and 800 rpm; the finished ink is adjusted to 14–18 tack units for paper stocks from 80–170 g/m². Fountain solution pH is maintained at 5.0–5.5 because free calcium extraction accelerates above pH 6.0; varnish formulations with low free-phenol content and low hygroscopic rosin esters reduce moisture uptake and limit water-train redeposition. Compliance for folding cartons, brochures, magazine covers, and pressure-sensitive labels includes ISO 2846-1:2022 for process inks and ISO 12647-2:2013 for printing-condition control; spot-colour rubine is outside the CMYK characterisation set and is therefore held to customer-specific CIELAB DE*ab tolerances, commonly ≤1.5. This pigment is not intended for direct food-contact printed surfaces unless a low-migration coating or barrier is validated under Regulation (EU) No 10/2011 or FDA 21 CFR 176.170 for the final printed structure.
During twin-screw compounding of rigid PVC, a 0.8 wt% addition of the calcium lake shifts the fusion torque curve because the pigment particles alter wall friction in the feed zone and act as dispersed nucleation sites during gelation. The production sequence starts with a hot mixer at 110–120°C, followed by a cooling mixer discharging below 45°C; the dry blend is converted on a counter-rotating twin-screw extruder with an L/D ratio of 25:1, barrel zone temperatures from 160°C to 190°C, and die temperature of 195–210°C. Addition ratios for opaque red sheet and profile applications generally fall between 0.3 wt% and 1.2 wt%; loadings above 1.5 wt% have shown plate-out and surface streaking in production runs when the stabiliser package is calcium-zinc based. Heat stability is assessed through EN 12877-1 using a two-roll mill at 190°C; colour change is then evaluated under ISO 105-A02 to confirm that early lake decomposition does not shift shade toward a yellowed red. For external-facing articles, tint lightfastness is classified below 3 on ISO 105-B02, which excludes unpainted exterior use. End products include rigid PVC calendered film for card overlays, document covers, decorative laminates, and point-of-sale panels; regulatory obligations include REACH and, when the final article is intended for toys, EN 71-3:2019 migration limits for barium, cadmium, lead, and chromium. The pigment is not recommended for semi-rigid PVC gaskets under continuous contact with plasticiser oils because migration under load is not well characterised in published data for this specific configuration.
The 8–12 wt% addition of Lithol Rubine 8B in surface-printed vinyl shrink sleeves is dispersed in a polyvinyl butyral or vinyl chloride-vinyl acetate copolymer vehicle before reduction to press viscosity. Downstream production begins with a high-speed dissolver premix in an ester/ketone lacquer, followed by a horizontal bead mill charged with 0.6–1.0 mm ceramic media until fineness on ISO 1524:2013 remains below 5 µm. On gravure presses, electro-mechanically engraved cylinders transfer the reduced ink to PVC or PETG shrink films at 200–300 m/min; drying tunnels at 60–70°C remove the solvent, but the calcium lake increases total solvent retention compared with high-molecular-weight polycyclic reds at equal film weight. Dry film weights are therefore held to 1.2–1.6 g/m² and residual solvent is checked by EN 13628-1:2002 headspace gas chromatography. Compliance for shrink sleeves used in cosmetics, beverage labels, and tamper-evident seals is structured around ISO 12647-4:2014 for gravure process control, REACH, and the EuPIA GMP framework; for food-contact sleeve constructions, Regulation (EU) No 10/2011 or FDA 21 CFR 175.300 must be evaluated for the printed layer, because pigment-level migration data alone do not establish final packaging compliance. Operational limits include avoiding alcohol-rich solvent blends above 30 wt% isopropanol in the letdown vehicle, which can destabilise the calcium-lake dispersion and produce grinding streaks during extended press runs.
Before lot certification is released, Lithol Rubine 8B intended for lip and cheek products must be confirmed as D&C Red No. 7 Calcium Lake under FDA 21 CFR 74.1307 and listed as CI 15850 in Annex IV to Regulation (EC) No 1223/2009; the Annex IV field-of-application column excludes products intended for the eye area. Typical addition ratios are 4–10 wt% in lipsticks and liquid lip products, 1–3 wt% in pressed powder blush, and 0.5–1.5 wt% in tinted lip balms. The production process at the colour cosmetics manufacturer begins with pigment press cake pre-dispersion in castor oil or octyldodecyl stearoyl stearate at 75–85°C in a vacuum homogeniser, followed by triple-roll milling to reduce aggregates below 20 µm; drawdown fineness is checked by ISO 1524:2013. The waxy base is combined at 80°C, filled into moulds at 70°C, and cooled at 4–10°C to lock the colourant distribution. Batch certification under FDA 21 CFR 74.1307(b) imposes heavy metal maxima, including lead ≤20 mg/kg, arsenic ≤3 mg/kg, and mercury ≤1 mg/kg, measured on the certified lot. Terminal products include lipsticks, rouge, pressed cheek powder, and tinted lip balms; manufacturers must also maintain REACH records for the non-cosmetic handling environment and avoid any lot that fails the EU Annex IV purity criteria. Because the lake is moderately sensitive to oxidation in open pan systems, lip products are processed under vacuum and blanketed with nitrogen when batch size exceeds 50 kg.
In injection-moulded polypropylene closures, Lithol Rubine 8B is applied at 0.5–2.0 wt% in the final part, most often through a 25–30 wt% pigment masterbatch in a low-density polyethylene or polypropylene carrier. The downstream process is a co-rotating twin-screw extruder with an L/D ratio of 40:1, screw speed of 400–600 rpm, and melt temperature maintained at 200–220°C; the masterbatch is let down at 2–4 wt% into natural PP resin at the injection moulding machine. Because PR57:1 decomposes above 230°C, the barrel temperature profile must not exceed 225°C, and residence time is kept below 5 min to avoid gas formation and screw deposit accumulation. Pre-drying of the carrier is required at 80°C for 4 h when storage RH exceeds 60% to prevent moisture-induced viscosity loss in the masterbatch. Melt flow is checked according to ISO 1133-1:2022 with a 2.16 kg load at 230°C; tensile and impact properties are verified by ASTM D638-14 and ISO 180:2019, respectively. End products include PP beverage caps, cosmetic closures, and non-food container lids. Compliance requires REACH and, when the closure is part of an electrical appliance, RoHS Directive 2011/65/EU; for food-contact closures, Regulation (EU) No 10/2011 and FDA 21 CFR 178.3297 colourant clearance must be confirmed through migration testing because the pigment is not established for all direct food-contact saturation conditions. The grade is not recommended for outdoor furniture or automotive exterior components because tint lightfastness is below 3 on ISO 105-B02 and migration in unpainted polyolefin matrices remains a documented operational boundary.
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Lithol Rubine 8B is a commercial grade designation generally mapped to C.I. Pigment Red 57:1, C.I. Constitution Number 15850:1, CAS 5281-04-9, EC 226-109-5. The pigment is a calcium lake of 4-[(4-methyl-2-sulfophenyl)azo]-3-hydroxy-2-naphthalenecarboxylic acid, with molecular formula C18H12CaN2O6S and molecular weight 424.44 g/mol. The monoazo lake provides a blue-red rubine mass tone and high tinting strength in full shade. Relative tinting strength determined by ISO 787-24 is typically 95–105 % of the manufacturer reference standard. The term “8B” is not a fixed universal specification; surface-treated and untreated calcium lake grades differ in oil absorption, agglomerate size, dusting behaviour, and residue content. Manufacturer technical data sheets commonly report density in the range 1.40–1.52 g/cm³ and tamped bulk density between 0.25 and 0.50 g/cm³.
Specific surface area by nitrogen adsorption according to ISO 9277:2010 is typically between 20 and 45 m²/g for high-strength ink grades and 10–20 m²/g for opaque plastics grades. Higher surface area increases tinting strength but may reduce flow in high-solids coatings unless dispersant demand is satisfied. Oil absorption according to ISO 787-5:1980 is reported in the range 40–55 g/100 g for surface-treated ink grades. Residual volatile matter at 105°C according to ISO 787-2:1981 is typically held below 1.5 %.
| Parameter | Test method | Typical published range for PR 57:1 |
|---|---|---|
| Density | ISO 787-10 | 1.40–1.52 g/cm³ |
| Oil absorption | ISO 787-5:1980 | 40–55 g/100 g |
| pH of aqueous extract | ISO 787-9:1981 | 6.5–8.0 |
| Volatile matter at 105°C | ISO 787-2:1981 | ≤1.5 % |
| Residue on 45 µm sieve | ISO 787-7:1981 | ≤0.1 % |
| Lightfastness full shade | ISO 105-B02 | 4–5 blue wool |
| Lightfastness 1:10 TiO2 | ISO 105-B02 | 2–3 blue wool |
| Heat stability in polyolefins | Internal TGA/DSC | 240–260 °C |
Values are typical technical-data-sheet ranges for surface-treated ink and plastics grades; they are not absolute specifications and should be confirmed against the supplier certificate of analysis for a specific batch.
The controlling variables are peak melt temperature, local viscous dissipation, and residence time under shear. In co-rotating twin-screw extruders with L/D ratios of 44:1 to 52:1 and screw speeds between 400 and 800 min⁻¹, melt temperature at the die plate may remain below 230°C while pigment-polymer interfacial temperatures exceed the threshold at which the calcium lake loses water of crystallisation. The resulting micro-void formation and shade drift toward yellow-red are not reversed by let-down dilution. Feeder starvation that extends residence time beyond 120 s is associated with increased blooming in low-density polyethylene film and with plate-out on vacuum venting equipment. Pre-drying to 0.15 % volatile matter is applied when ambient relative humidity exceeds 60 % because free moisture accelerates hydrolysis of the lake during melt processing. Filtration pressure rise across screens of 20 µm aperture indicates residual agglomerates; additional shear is frequently insufficient, and reformulation with a low-molecular-weight polyethylene wax at 2 to 4 wt% relative to pigment is required. In injection moulding with clamp force settings above 800 kN and barrel temperatures of 200–240°C, the pigment is usually introduced as a pre-dispersed masterbatch at 40–50 wt% in LDPE or PP carrier. Colouristic consistency of the moulded part depends on back pressure of 20–30 bar and screw-recovery time below 8 s; longer recovery times at low speed can induce localised overheating at the non-return valve.
For conventional sheet-fed offset printing, PR 57:1 is dispersed in a rosin-modified phenolic varnish at pigment loadings between 15 and 22 wt%. Because the lake has higher oil absorption than quinacridone magenta grades, three-roll mill grinding may require two to three passes at 25°C to reach a grind gauge reading below 10 µm. The shade in aqueous fountain contact is pH-sensitive; fountain solution buffered to 4.8–5.2 prevents bronzing and loss of transparency that appear when pH exceeds 8.5. In toluene/ethyl acetate gravure inks, the pigment is used in nitrocellulose/polyurethane binders at pigment loadings between 8 and 12 wt% in a 70:30 solvent blend to reduce plate blocking. Printed density stabilises in laboratory drawdowns at 1.35–1.50 on coated paper at 2.0 g/m² dry film weight when evaluated under ISO 2834-1:2020, though published line-speed data for this grade remain limited. Aqueous flexographic inks should maintain vehicle pH below 9.0 before pigment addition; pre-wetting the presscake with a nonionic surfactant at 5–10 wt% based on pigment improves colour development.
PR 57:1 occupies a cost-sensitive position between barium/calcium BONA lakes such as C.I. Pigment Red 48:2 and high-lightfastness quinacridone magentas such as C.I. Pigment Red 122. PR 57:1 contains no chlorine substituent, whereas PR 48:2 contains a chlorine-substituted aryl group. The azo lake structure provides strong flop and clean rubine tint in short-oil alkyd and nitrocellulose lacquers, but exterior durability is inferior. Accelerated weathering under ISO 16474-2 or ASTM G155 Cycle 1 demonstrates that PR 122 retains colour stability beyond 2000 h in exterior coatings, while PR 57:1 is normally limited to interior or limited-exposure decorative systems. Alkali resistance is restricted; contact with aqueous media above pH 8.5 causes shade drift and bronzing. For solventborne packaging coatings, PR 57:1 may be selected over PR 48:2 when lower chlorine content is required by a converter specification, provided that migration testing under EU Regulation 10/2011 or 21 CFR 178.3297 conditions is performed on the finished film.
Comparative relative performance ranges derived from manufacturer technical data sheets are shown below.
| Property | PR 57:1 | PR 48:2 | PR 122 |
|---|---|---|---|
| Chemical class | Calcium monoazo lake | Calcium monoazo lake | Quinacridone |
| Chlorine substituent | Absent | Present | Absent |
| Lightfastness full shade | 4–5 blue wool | 3–4 blue wool | 7–8 blue wool |
| Lightfastness 1:10 TiO2 | 2–3 blue wool | 2 blue wool | 7 blue wool |
| Heat stability in polyolefins | 240–260 °C | 250–270 °C | 300 °C |
| Alkali resistance | Limited | Moderate | Good |
| Cost position | Low | Low | High |
For regulatory conformity, the grade must be specified by supplier documentation because surface treatments and trace impurity levels affect compliance. Heavy metal content in packaging is typically assessed against EU Directive 94/62/EC, where the sum of lead, cadmium, mercury, and hexavalent chromium must not exceed 100 mg/kg. When used in toys or childcare articles, migration limits under EN 71-3 apply; PR 57:1 is not automatically compliant in all tinting levels and must be tested in the final article. Under EU REACH Regulation 1907/2006, the substance may be subject to registration and safety data sheet obligations; it is not presently identified as a substance of very high concern. FDA food-contact admissibility under 21 CFR 178.3297 may apply to certain polymer colourants, but not all surface-treated grades meet the purity criteria; confirmation against the finished article extraction limits in 21 CFR 177 or EU 10/2011 is required before food packaging use. In cosmetic applications, PR 57:1 is designated CI 15850:1 and is subject to purity criteria for barium, calcium, and aromatic amines under Regulation (EC) No 1223/2009; industrial rubine 8B grades should not be substituted without a certified purity file.
Substitution in calendered flexible PVC requires evaluation of plasticizer bleed and stabiliser interactions. PR 57:1 differs from PR 48:2 in dispersibility and oil absorption because the calcium lake typically has a finer agglomerate structure after finishing. In plastisols formulated with DINP or DIDP at 40–60 phr, high-shear dissolvers or three-roll mills are used; dispersion temperature should be maintained below 40°C to avoid premature solvation of the PVC resin. The grade is compatible with barium-zinc and calcium-zinc stabiliser packages at typical doses of 2–4 phr; however, tin mercaptide stabilisers may accelerate shade drift through sulphur-alkali interactions. The product should not be combined with amine-based additives in solventborne systems because amine salts can disrupt the lake structure. Pre-dispersed pigment chips are preferred for calendering to minimise dust and agglomerates. If the replacement is made at equal pigment volume concentration, colour strength may require adjustment because PR 57:1 is stronger in tint than PR 48:2; let-down with titanium dioxide at 1:10 may show higher chroma but lower lightfastness. Migration testing on the plastisol film should follow EN 71-10 or EN 71-11 depending on the intended end use.
Migration and blooming in LDPE film are governed by pigment solubility in the matrix, dispersion quality, and film cooling rate. PR 57:1 has a planar monoazo calcium lake structure that can re-agglomerate under slow quench conditions, producing surface haze and rub-out colour shift. In blown film extrusion with a 60 mm single-screw extruder and 30:1 L/D, die temperature set between 180 and 200°C, and blow-up ratio 2.5:1, high-contrast white substrate contact testing may show visible transfer if pigment loading exceeds 2.0 wt%. The effect is reduced by using a polyethylene wax at 2–3 wt% based on pigment weight and by increasing screw backpressure to 120–150 bar. If the film is intended for fatty food contact, extraction testing under EU Regulation 10/2011 with olive oil or authorised simulants should be conducted because the pigment is not universally listed for direct food-contact use.
In polycarbonate and acrylic, PR 57:1 is rarely used because processing temperatures above 260°C degrade the lake; quinacridone or diketopyrrolopyrrole grades are selected for these matrices. If PR 57:1 is used in ABS at processing temperatures of 220–240°C, pre-dried resin and pigment are required, and the compound should not be purged with amine-containing cleaning agents.