| HS Code | 472013 |
| Product Name | Permanent Orange GY |
| Colour Index Name | C.I. Pigment Orange 34 |
| Colour Index Number | 21115 |
| Cas Number | 3520-72-7 |
| Chemical Class | Disazo (diarylide) organic pigment |
| Chemical Formula | C34H28Cl2N8O2 |
| Molecular Weight | 651.55 g/mol |
| Appearance | Orange powder |
| Hue | Yellowish orange |
| Specific Gravity | 1.35–1.45 g/cm³ |
| Oil Absorption | 35–45 g/100 g |
| Ph | 6–8 |
| Moisture Content | ≤1.0% |
| Heat Resistance | 180–200 °C |
| Lightfastness | 6–7 full shade; 5–6 tint |
| Weather Fastness | 4–5 |
| Acid Resistance | Good |
| Alkali Resistance | Good |
| Water Resistance | Good |
| Solvent Resistance | Good |
| Migration Resistance | Good |
| Typical Applications | Printing inks, paints, plastics, textile printing |
As an accredited Permanent Orange GY factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Permanent Orange GY is packed in sealed 25 kg moisture-resistant fiber drums with inner polyethylene liners for safe storage and transport. |
| Container Loading (20′ FCL) | Permanent Orange GY is packed in sealed drums, palletized and securely braced inside a 20′ FCL container for ocean shipment. |
| Shipping | Permanent Orange GY should be shipped in sealed, properly labeled containers, kept dry and away from oxidizers. Follow the supplier’s SDS and applicable ADR/IMDG/IATA rules for classification and documentation. If confirmed non-hazardous, it may move as general chemical cargo; otherwise use the specified UN number and packing. |
| Storage | Store Permanent Orange GY in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and moisture. Keep containers tightly closed, clearly labeled, and upright. Segregate from strong oxidizers, acids, and bases. Use secondary containment, avoid dust generation, and follow local regulations and the SDS. |
| Shelf Life | Permanent Orange GY is typically stable for 24 months when stored in a cool, dry, well-ventilated area in tightly closed containers. |
Solvent-based flexographic and gravure inks intended for coated paperboard packaging use Permanent Orange GY as the press-ready colourant in a nitrocellulose-polyurethane or polyvinylbutyral resin vehicle at a finished-ink pigment loading of 8–12 wt%. The dispersion sequence begins with a high-speed pre-mix at 15–18 m/s peripheral tip speed, followed by a horizontal bead mill charged with 0.4–0.6 mm yttrium-stabilized zirconia beads; grind fineness is controlled by a grind gauge at 10 µm maximum before let-down and press viscosity adjustment to 18–25 s DIN cup 4 mm at 25 °C with ethyl acetate/isopropanol blends. Batch release testing is specified against EN ISO 787-2:2005 for volatile matter and EN ISO 787-5:2015 for oil absorption; when the printed structure enters food-contact use, the converter must validate the finished article under Regulation (EC) No 1935/2004 and, for paperboard, the Swiss Ordinance SR 817.023.21 or German BfR Recommendation XXXVI if applicable, while the pigment itself must satisfy the EuPIA Exclusion Policy and REACH Annex XVII entry 43 through extractable amine testing. On narrow-web flexo presses running above 250 m/min, operational experience indicates that shade drift and anilox cell plugging occur when press viscosity falls below 15 s and ink temperature exceeds 40 °C, requiring stainless-steel anilox rolls with trihelical engraving and ceramic surfaces. Terminal printed articles include form-fill-seal snack wrappers, pre-printed corrugated trays, paper carrier bags, and outer cartons for fast-moving consumer goods.
Permanent Orange GY is predispersed at 25–35 wt% pigment in low-density polyethylene or EVA carrier masterbatch on a co-rotating twin-screw extruder with L/D 40–44; the final injection-moulding or extrusion let-down is typically 0.2–1.0 wt% pigment in the polymer matrix. The melt temperature in the last screw zone is maintained at 180–200 °C and residence time is held below 60 s; above 200 °C, the diarylide azo chromophore begins to degrade with a measurable increase in releasable restricted aromatic amine formation, making the material unsuitable for engineering thermoplastics processed above 240 °C such as ABS or polycarbonate. In production, the pigment is fed through a side feeder after the polymer melt point to reduce shear history, and dispersion quality is checked by filter pressure rise across a 5 µm screen pack on a single-screw laboratory extruder; published data for this specific configuration is limited, so in-plant correlation with EN 12877-1:1999 heat stability and EN 13900-5:2005 dispersibility is required. Compliance for plastics articles intended for electrical and electronic equipment is assessed under RoHS Directive 2011/65/EU, while articles submitted to toy safety protocols require EN 71-3:2019+A1:2021 extractable-metal migration; food-contact polymer applications are excluded unless specific migration of restricted amines is demonstrated below detection limits under Regulation (EU) No 10/2011. Finished moulded components include industrial crates, pails, closures, caps, and non-food packaging sheets.
| Process stage | Equipment type | Indicative window | Control method |
|---|---|---|---|
| Pigment pre-drying | Vacuum tray dryer | 65–70 °C, 4–6 h, residual moisture ≤1.0% | EN ISO 787-2:2005 |
| Masterbatch compounding | Co-rotating twin-screw extruder, L/D 40–44 | Melt temperature 180–200 °C, residence time ≤60 s | Melt probe, EN 12877-1:1999 |
| Let-down injection moulding | Reciprocating screw, L/D 20–24 | Melt temperature 180–200 °C, back pressure 5–10 bar | ISO 1133-1:2022 |
| Dispersion assessment | Single-screw extruder, 5 µm screen pack | Filter pressure rise ≤1.0 MPa | EN 13900-5:2005 |
Medium-oil alkyd gloss enamels and solvent-borne industrial primers incorporate Permanent Orange GY at 4–10 wt% of total wet coating mass, with the pigment volume concentration kept below the critical pigment volume concentration to preserve high gloss and film integrity. The grind phase is carried out on a high-speed disperser equipped with a saw-tooth impeller at 18–25 m/s tip speed in a short-oil alkyd or urethane-modified alkyd vehicle; the batch is discharged to a horizontal bead mill or triple-roll mill when a Hegman gauge reading of 5–6 is achieved, avoiding residual seediness at brush viscosity. The final coating is tested under ISO 2813:2014 for 20° specular gloss and under ISO 787-24:1998 for relative tinting strength; the solvent-borne system must meet the VOC limits of Directive 2004/42/EC in the applicable decorative paint category, while the pigment itself is evaluated under REACH Annex XVII entry 43 for restricted aromatic amine release. This pigment is not suited to continuous exterior exposure in two-coat architectural systems: lightfastness is acceptable for indoor and short-cycle outdoor decorative use, but long-term exterior chalk and fade resistance is insufficient for automotive or façade-grade topcoats unless additional ultraviolet barriers are laminated or overcoated. Finished products include alkyd wall enamels, industrial maintenance primers, aerosol enamels, and pigmented wood coatings.
Aqueous pigment printing pastes for cotton and polyester-cotton knitgoods require Permanent Orange GY to be predispersed as a surfactant-stabilized aqueous paste and metered at 5–12 wt% dry pigment on paste mass, with an acrylic or styrene-butadiene binder at a binder-to-pigment ratio of 2.0–2.8:1 and a synthetic thickener to adjust print viscosity to 30–40 dPa·s at 20 °C on a Brookfield RVT spindle 4 at 4 rpm. The paste is applied through flat or rotary screen printing equipment with mesh counts from 80–125 mesh, followed by drying at 120–150 °C and cure at 150 °C for 3–5 min in a hot-air belt dryer; after washing, fastness is verified under ISO 105-C06:2010 and dry/wet crocking under ISO 105-X12:2016. Because the pigment is derived from a benzidine analogue, textile wet-processing lines must screen every production lot under EN ISO 14362-1:2017 before use; brands may additionally require OEKO-TEX Standard 100 Annex 4 verification, and the EU restricts the sale of textile articles that release listed aromatic amines under REACH Annex XVII entry 43. Discharge printing and reductive flock destruction are contraindicated because reducing agents can cleave the azo bond and release the free aromatic amine. Finished textile articles include printed T-shirts, canvas tote bags, upholstery backings, and home-textile panels.
| Obligation | Normative method | Endpoint | Control position |
|---|---|---|---|
| REACH Annex XVII entry 43 | EN ISO 14362-1:2017 | Restricted aromatic amines | Not detected above method detection limit |
| OEKO-TEX Standard 100 Annex 4 | EN ISO 14362-1:2017 | Restricted aromatic amines on printed textile | Not detected |
| Wash fastness | ISO 105-C06:2010 | Shade change and staining | ≥4 shade change, ≥3–4 staining |
| Crocking fastness | ISO 105-X12:2016 | Dry and wet staining | ≥4 dry, ≥3 wet |
When plasticized PVC film is produced on a four-roll inverted-L calender, Permanent Orange GY is introduced at 0.3–1.5 phr based on PVC resin, either as a pre-dispersed plasticizer paste or as a PVC-based masterbatch at 20 wt% pigment. The dry-blend is mixed in a high-speed hot mixer to 110–120 °C, then fluxed on a two-roll mill at 160–170 °C and calendered at 150–170 °C; under these conditions, the pigment exhibits acceptable short-term heat stability, but extended residence above 180 °C can initiate decomposition and should be avoided. Plate-out on calender rolls is the primary process defect associated with this pigment class: it is minimised by using metal-free stabiliser packages, controlling free organic acid content, and specifying a methyl methacrylate-based processing aid at 1–2 phr. Compliance for non-food flexible PVC articles is verified under RoHS Directive 2011/65/EU for heavy metals and, where toy contact is possible, under EN 71-3:2019+A1:2021; food-contact PVC films under Regulation (EU) No 10/2011 are not recommended unless migration of restricted aromatic amines is demonstrated below the detection limit using an accredited method. Terminal products include calendered tablecloths, PVC tarpaulins, warning tapes, flooring wear-layer films, and pool liners.
For sulfur-cured natural rubber and styrene-butadiene rubber compounds, Permanent Orange GY is added at 1–3 phr during masterbatch mixing in an intermesh internal mixer at 40–60 rpm rotor speed and 90–110 °C dump temperature; the pigment is incorporated after the elastomer has masticated but before sulfur and accelerators are added to avoid premature cure influenced by pigment pH. In compounded natural latex, a 30% aqueous pigment dispersion is prepared by ball-milling with anionic naphthalene sulfonate dispersants for 24–48 h, then metered into latex at 0.5–2.0 phr before coagulant dipping or casting. Cured rubber articles are tested under ISO 23529:2021 for general handling and, where children’s toys are involved, under EN 71-3:2019+A1:2021 for extractable elements; food-contact rubber applications under 21 CFR 177.2600 are not supported unless the pigment is explicitly listed for the intended use, and published data for this specific configuration is limited. Finished products include rubber mats, extruded EPDM profiles, latex balloons, and elastic bands.
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Permanent Orange GY is the commercial trade designation for C.I. Pigment Orange 43, a polycyclic perinone organic pigment supplied as a dry powder for high-temperature resin systems, industrial coatings, and selected printing ink applications. The colour index number is 71105; the CAS registry number is 4424-06-0. Public trade literature identifies the product as a yellow-shade orange with high thermal stability and low migration tendency in semicrystalline and amorphous thermoplastics. Commercial specifications for Permanent Orange GY are controlled by lot-specific certificates that normally report tinting strength relative to a master standard, pH in aqueous extract by ISO 787-9, oil absorption by ISO 787-5, and residue on a 45 µm sieve by ISO 787-7. The trade designation does not encode a separate model suffix in standard technical literature; regional suppliers may offer equivalent perinone chemistry under different trademarks, but the colour index classification remains C.I. Pigment Orange 43.
The primary differentiation from monoazo and disazo orange pigments is thermal and migration behaviour. C.I. Pigment Orange 43 retains colour strength after compounding in polypropylene at 300 °C according to published fastness tables, whereas C.I. Pigment Orange 13 is generally limited to processing below 200 °C. The difference is chemical rather than formulation-dependent. The perinone polycyclic structure resists oxidative attack and avoids low-molecular-weight decomposition fragments that cause hue drift, plate-out, or contact staining in engineering resins. Consequently, Permanent Orange GY is specified where moulders operate hot-runner systems with extended residence times or where deposits on gate surfaces and vents create downstream quality defects.
When Permanent Orange GY is processed in polypropylene at 300 °C, the observed failure mode is not melt-phase decomposition of the perinone ring but surface plate-out and hue shift caused by incomplete dispersion or resin oxidation. Thermal stability testing under EN 12877-2 uses injection moulding with controlled melt temperature and residence time; the standard reports colour difference after processing. In high-temperature polyamides and polycarbonates, process validation is performed by comparing colour difference after conditioning to a ΔE*ab no greater than 1.5 units against an unprocessed standard plaque. Published fastness tables classify C.I. Pigment Orange 43 as having heat resistance of 300 °C in polyolefins and 300 °C to 320 °C in polycarbonate; exact retention depends on residence time, shear input, and oxygen ingress during compounding.
In polycarbonate and polyamide compounding on co-rotating twin-screw extruders with L/D 32:1–44:1, Permanent Orange GY is introduced via masterbatch or pre-dispersed powder at 0.1 wt% to 1.5 wt%. The processing window is set by the resin rather than the pigment; pigment degradation is not the limiting factor in unreinforced polycarbonate at 280 °C. However, dispersion quality is a separate constraint. Agglomerates that survive the screw mixing zone appear as dark specks in thin-wall mouldings. For critical applications, filter pressure rise on the extruder screen pack is monitored; a pressure increase greater than 10% over 30 min indicates either agglomerated pigment or insufficient wetting. Published data for this specific configuration is limited where glass-fibre or mineral-filled systems are used because abrasive wear can alter particle size distribution under production shear.
Accelerated weathering of Permanent Orange GY in thermosetting powder coatings is assessed by ISO 4892-2 cycles with xenon arc irradiance at 0.51 W/m² at 340 nm, black-standard temperature 65 °C, and water spray. The pigment contributes chromatic stability, but coating gloss and binder degradation often dominate total colour shift. In polyester/TGIC and polyester/β-hydroxyalkylamide systems, perinone pigmentation generally shows lower ΔE than arylamide or disazo pigment alternatives in exterior exposure. The pigment is not a UV stabilizer; resin stabilizer packages remain necessary for gloss retention and resistance to chalking. For lightfastness, the accelerated test is ISO 105-B02; the pigment is typically rated 7–8 at full shade after 100 h exposure.
Lightfastness ratings are test-method dependent and do not transfer directly to long-term exterior durability without weathering validation. In thin films with low pigmentation below 0.05 wt%, lightfastness may be compromised by inadequate UV absorption; full-shade ratings should not be extrapolated to deep tint reductions. For powder coatings, extrusion conditions must be controlled below the crosslinking initiation temperature of the resin. A typical extrusion zone temperature of 90 °C to 110 °C is used for premix dispersion before curing; higher temperatures can cause premature crosslinking and gloss loss in the final film.
For coil and powder coating applications, the pigment is dispersed in the binder before extrusion or milling. The grind is controlled by fineness of grind under ISO 1524; a final value below 10 µm is typical for air-drying alkyd and two-component polyurethane systems. Viscosity during dispersion rises as agglomerates are wetted and then decreases as agglomerates separate; excessive heat generation above 60 °C in solventborne grinds can cause solvent loss and flocculation. In waterborne systems, amine-neutralized dispersants are preferred because the pigment surface is hydrophobic; however, residual amine in the dried film can accelerate binder yellowing and should be minimised.
Dispersion of Permanent Orange GY in solventborne industrial coatings is carried out on high-speed dissolvers followed by bead milling. The oil absorption value by ISO 787-5 is relevant for formulation solids and pigment volume concentration; commercial values are lot-specific, but values near 35 g/100 g to 45 g/100 g are typical for perinone grades. Tinting strength is evaluated against a controlled master standard by ISO 787-24. Colourimetric equivalence to the master standard is commonly expressed as ΔE*ab; supplier certificates generally set an upper limit of 1.0 unit for standard powder deliveries. These values are not direct predictors of final article colour, because processing temperature, resin stabilizer package, and particle size distribution shift the effective absorption coefficient.
| Attribute | C.I. Pigment Orange 43 Permanent Orange GY |
C.I. Pigment Orange 34 Disazo condensation |
C.I. Pigment Orange 36 Benzimidazolone |
C.I. Pigment Orange 13 Disazo |
|---|---|---|---|---|
| Heat resistance in polyolefin | 300 °C | 200 °C | 220 °C | 180 °C |
| Lightfastness, ISO 105-B02, full shade | 7–8 | 7 | 6–7 | 4–5 |
| Migration resistance in plasticized PVC | 5 | 4–5 | 4–5 | 2–3 |
| Typical application area | Engineering plastics, exterior coatings, high-temperature polyolefins | Rigid PVC, polyolefins, industrial coatings | Plastics, architectural coatings | PVC, printing inks |
Replacement of C.I. Pigment Orange 73 with Permanent Orange GY in polyamide extrusion is driven by raw-material cost and available supply. Both pigments survive polyamide processing at 300 °C, and both are rated high for migration resistance. The principal penalty is tinctorial strength: perinone orange typically requires higher loading than DPP to reach the same colour strength at equal film thickness. Published data for this specific configuration is limited; the appropriate comparison is a strength curve generated in a laboratory two-roll mill and then verified on the production extruder. Differences from C.I. Pigment Orange 34 and C.I. Pigment Orange 36 are more pronounced at high processing temperatures. In polyamide at 300 °C, disazo condensation and benzimidazolone pigments may shift hue or lose chroma, while perinone remains stable. In rigid PVC processed below 200 °C, the performance gap is smaller, and lower-cost disazo pigments may be adequate.
Compared with molybdate orange, C.I. Pigment Red 104, Permanent Orange GY is free of lead and hexavalent chromium and therefore falls outside the restrictions in RoHS Directive 2011/65/EU Annex II. The operational boundary is opacity. Lead molybdate pigments provide higher hiding power and lower cost; organic perinone pigments have lower opacity and require higher dosage or a titanium dioxide base to reach equivalent coverage. In polycarbonate injection moulding at 290 °C melt temperature, Permanent Orange GY is typically dosed as a 20% masterbatch; the concentrate is pre-dried with the resin at 120 °C for 4 h when ambient relative humidity exceeds 60%. Residual moisture above 0.02% in polycarbonate causes surface splay and gloss reduction independent of pigment chemistry. The processing limit is set by the base polymer, not by the perinone chromophore.