| HS Code | 276674 |
| Productname | Disperse Violet 57 |
| Casnumber | 12217-95-7 |
| Colorindexname | C.I. Disperse Violet 57 |
| Colorindexnumber | 60751 |
| Chemicalclass | Azo disperse dye |
| Molecularformula | C20H19N5O4 |
| Molecularweight | 393.40 g/mol |
| Appearance | Violet powder |
| Physicalstate | Solid |
| Solubilityinwater | Insoluble |
| Solubilityinorganicsolvents | Soluble |
| Application | Dyeing and printing of polyester fibers |
| Dyeingmethod | High-temperature high-pressure exhaust dyeing, carrier dyeing, thermosol dyeing, and transfer printing |
| Lightfastness | 6 |
| Washingfastness | 4-5 |
| Sublimationfastness | 4-5 |
| Phvalue | 6.0-8.0 (1% dispersion) |
| Moisturecontent | ≤1.0% |
| Packaging | 25 kg fiber drum with inner plastic bag |
| Storageconditions | Cool, dry, well-ventilated place, away from light |
| Shelflife | 24 months |
As an accredited Disperse Violet 57 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Disperse Violet 57 packaging: 25 kg moisture-resistant, double-walled fiber drums with sealed inner polyethylene liners. |
| Container Loading (20′ FCL) | Disperse Violet 57 is palletized and loaded into a 20′ FCL container, securely sealed for safe, compliant ocean shipment. |
| Shipping | Disperse Violet 57 is shipped as a non-hazardous textile dye in sealed, labeled containers. Transport and store in a cool, dry, well-ventilated area away from strong oxidizers and direct sunlight. Protect from moisture and physical damage; no special UN transport classification applies unless local regulations specify otherwise. |
| Storage | Store Disperse Violet 57 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and strong oxidizers. Keep containers tightly closed, clearly labeled, and upright; prevent dust generation and moisture ingress. Segregate from incompatible materials and protect from physical damage. Use appropriate personal protective equipment and follow the supplier’s safety data sheet. |
| Shelf Life | Shelf life is typically 24 months under recommended storage conditions: cool, dry, dark, well-ventilated, and away from incompatible materials. |
In high-temperature exhaust dyeing of polyester warp knits, the processing window for C.I. Disperse Violet 57 is controlled by dispersion stability and fibre accessibility above the glass transition. A production-scale jet dyeing machine operated at a liquor ratio of 1:8 to 1:15 shows levelling failure and specking when the dye dispersion contains aggregates larger than 1 μm, measured by laser diffraction per ISO 13320; such aggregates collect in stagnant boundary layers at the folded edges of warp-knit beams and overflow compartments. Predispersed liquid brands are therefore used, or powder dye is pre-pasted with naphthalene sulfonate condensate or lignosulfonate dispersant at 0.5–2.0 g/L before injection through 25 μm wedge-wire screens. The dyebath is buffered with acetic acid/sodium acetate to pH 4.5–5.5; excursions above pH 6.0 reduce exhaustion and dull the violet shade. The temperature is raised at 1–2 °C/min to 130 °C and held for 30–45 min, with the shorter hold reserved for pale depths below 0.5% o.w.f. After dyeing, the knitted fabric is reduction cleared with sodium dithionite at 2–3 g/L and sodium hydroxide at 2–3 g/L at 70–80 °C for 20 min, neutralized, and hot-rinsed to remove surface dye and dispersant residues that depress rub fastness. Automotive seat covers and technical sportswear dyed with this route are assessed against ISO 105-C06:2010, ISO 105-B02:2014, ISO 105-X12:2016, and ISO 105-E04:2013. In service water above 100 ppm CaCO₃, a sequestering agent is added prior to the dispersant to prevent calcium-induced flocculation. A recurrent production failure on hydrophobic warp knits is pressure differential increase across the filter bundle after three to four batches due to residual cationic softener; an anionic pre-scour with sodium carbonate is specified before dyeing.
Package dyeing machines equipped with reversible axial flow pumps impose a different constraint on C.I. Disperse Violet 57: the wound density of polyester filament yarn on perforated cones or tubes must be maintained between 0.36 g/cm³ and 0.42 g/cm³. Outside this range, differential pressure across the package rises above 1.0 bar at normal pump speed, and flow reversal produces core-to-edge shade variation even when the dyebath is fully exhausted. The machine is filled with water at 50–60 °C, and the dye is added as a 15–20% w/w liquid or as a pre-pasted powder dispersion through the dosing tank; direct powder addition to the main vessel has been observed to form lumps on the package face that remain until reduction clearing. Alternating inside-out and outside-in flow cycles of 3–5 min each are maintained through the heating phase, with a circulation rate of 30–50 L/kg fibre/min on high-density yarn packages. The dyebath is held at pH 5.0–5.5 with acetic acid, and excess dispersant is limited to 1 g/L because higher concentrations lower final exhaustion and increase reduction-clear loading. Exhaustion is completed at 130 °C for 30–60 min, followed by cooling to 80 °C and reduction clearing without unloading, using 2 g/L sodium dithionite and 2 g/L sodium hydroxide at 70–80 °C for 20 min. A final acid rinse with 0.5 mL/L acetic acid prevents alkaline residues that reduce needle heat resistance of sewing thread. Package-dyed polyester yarns for automotive embroidery and outdoor upholstery stitching are tested to ISO 105-B02:2014, ISO 105-C06:2010, and ISO 105-X12:2016.
When a woven polyester/cotton fabric is dyed continuously, C.I. Disperse Violet 57 is applied from a pad bath containing an anti-migrant such as polyacrylate or alginate at 5–15 g/L and a wetting agent at 0.5–1.0 g/L. The pad liquor is buffered to pH 4.5–5.5; combined pad baths containing urea must be checked for scorch tendency at thermofixation temperatures because urea decomposition can generate acidic by-products that shift the violet shade. A horizontal pad mangle with compensating rubber rollers runs at 60–70% pick-up; lower pick-up on tightly woven poplins causes dye migration during drying and produces listing or side-to-side shade variation. The fabric is pre-dried with infrared or cylinder dryers at 100–120 °C, then thermofixed on a pin stenter at 195–210 °C for 45–90 s. Residence time above 210 °C is avoided because thermal decomposition or sublimation of the dye reduces depth and fastness. After thermofixation, the cotton component is dyed with reactive or vat dyes in a second stage when the blend ratio requires a solid shade; the polyester component is otherwise left as the only coloured phase. The combined fabric is then reduction cleared, soaped, and tested to ISO 105-C06:2010 and ISO 105-X12:2016. European workwear programs often add ISO 15797:2018 industrial laundering fastness for polyester/cotton blends dyed with disperse dyes. The output is typically poly/cotton workwear or shirting.
Atmospheric beam dyeing of secondary cellulose acetate filament yarn with C.I. Disperse Violet 57 proceeds at a lower temperature than polyester and imposes a narrower pH window. The dyebath is set at 40 °C, buffered to pH 5.5–6.0 with acetic acid, and raised at 1 °C/min to 85 °C. Above 90 °C, the risk of surface saponification and loss of filament tenacity increases sharply; therefore, pressure dyeing is not used. A dispersing agent is required at 0.5–1.5 g/L, and the liquor ratio on a beam machine is commonly 1:15 to 1:20. Because dye uptake on acetate is slower than on polyester, the hold time at 85 °C is 45–60 min for medium-depth violet. After dyeing, the beam is rinsed warm, and, if the finished lining is specified for machine washing, a mild cationic afterfixing agent is applied; however, aftertreatment can shift the violet shade bluer, so the colour coordinates are verified by reflectance spectrophotometer before the fixation bath is discharged. Acetate linings and soft furnishings dyed with C.I. Disperse Violet 57 are tested to ISO 105-C06:2010, ISO 105-X12:2016, and ISO 105-B02:2014. Because light fastness on acetate is lower than on polyester, the dye is restricted to indoor end uses unless an ultraviolet absorber is co-applied.
For rotary or flat-screen printing of polyester fabrics, C.I. Disperse Violet 57 is dispersed in a stock paste based on a low-viscosity alginate or synthetic thickener. The required print paste viscosity is 3,000–8,000 mPa·s at 25 °C measured with a Brookfield viscometer, spindle 6, at 20 rpm; the exact value is matched to the screen mesh, with higher viscosity for fine lines and lower viscosity for large blotches. Flat-bed screen mesh counts of 90–135 threads/cm and rotary screen mesh counts of 80–125 mesh are typical for disperse printing; meshes below 60 mesh produce heavy paste deposition but reduce definition and may cause flushing of the violet shade after fixation. The print paste contains the dye dispersion at 1–4%, a mild acid donor such as tartaric acid to maintain pH 4.5–5.5, and a reduction inhibitor if residual reducing agents are suspected. After printing, the fabric is dried at 100–120 °C and fixed in a high-temperature steamer at 170–180 °C for 6–8 min for polyester; for blends with cotton, fixation conditions are adjusted only after the cotton print paste is combined. The fixed fabric is washed with sodium dithionite reduction clear at 70–80 °C, soaped, and dried. Printed polyester banners, flags, and outerwear panels are tested to ISO 105-C06:2010, ISO 105-B02:2014, and ISO 105-X12:2016. Outdoor printed goods are typically specified to ISO 105-B02 level 6 or higher.
| Process route | Operating window | Critical control point | Representative end use |
|---|---|---|---|
| High-temperature exhaust on polyester warp knits | 1:8–1:15 LR, 130 °C, 30–45 min, pH 4.5–5.5 | Dispersion particle size ≤1 μm; reduction clearing at 70–80 °C | Automotive seat covers, technical sportswear |
| Package dyeing of polyester yarn | 0.36–0.42 g/cm³ package density, 130 °C, 30–60 min | Differential pressure ≤1.0 bar; flow reversal 3–5 min | Sewing thread, embroidery yarn |
| Thermosol on polyester/cotton | Pad 60–70% pick-up, 195–210 °C, 45–90 s | Dryer migration control; upper temperature limit 210 °C | Workwear, shirting |
| Acetate beam dyeing | 85 °C, 45–60 min, pH 5.5–6.0 | Avoid ≥90 °C saponification; verify hue shift after aftertreatment | Linings, indoor soft furnishings |
| Polyester printing | 3,000–8,000 mPa·s, 170–180 °C, 6–8 min | Mesh count 80–125 rotary; reduction clear wash | Banners, flags, outerwear panels |
| Polyamide pale-depth dyeing | 98–100 °C, 30–60 min, 0.1–1.0% o.w.f. | Syntan aftertreatment 2–4% o.w.f., pH 4.0–4.5 | Lingerie trims, hosiery, lining tapes |
| Document / Standard | Endpoint / scope | Application condition |
|---|---|---|
| ISO 105-B02:2014 | Xenon arc light fastness | Automotive, outdoor printed goods |
| ISO 105-C06:2010 | Domestic/commercial laundering fastness | Washable polyester, blends, nylon |
| ISO 105-X12:2016 | Rub fastness, dry/wet | All coloured articles |
| ISO 105-E04:2013 | Perspiration fastness | Sports/technical apparel |
| ISO 15797:2018 | Industrial laundering | Workwear polyester/cotton |
| REACH Regulation (EC) No 1907/2006 Annex XVII | Restricted aromatic amines, chemical safety | All lots before EU import |
| OEKO-TEX Standard 100 | Consumer safety limits | Garment linings, hosiery |
On nylon 6,6 taffeta, C.I. Disperse Violet 57 can be applied at 0.1–1.0% o.w.f. for pale-to-medium violet shades, but wet fastness is inherently lower than on polyester because the dye remains superficially adsorbed and lacks reactive bonding. The dyebath is set at 40 °C, raised to 98–100 °C over 30–45 min, and held for 30–60 min at pH 5.0–5.5. A nonionic levelling agent at 1–2 g/L is necessary to cover barre on high-filament nylon tricot; anionic dispersants are minimized because they compete with dye uptake. After dyeing, the fabric is rinsed and treated with a formaldehyde-free synthetic tanning agent or stain-blocking agent at 2–4% o.w.f. and pH 4.0–4.5 at 70–80 °C for 20 min. Typically, this aftertreatment is specified to improve wash fastness by one to two grey scale steps, although the actual improvement depends on the syntan solids and application pH. The aftertreatment may reduce light fastness, so only indoor nylon applications such as lingerie trims, hosiery, and lining tapes are specified. Fastness is assessed with ISO 105-C06:2010, ISO 105-X12:2016, and ISO 105-B02:2014; dyeings above 1.0% o.w.f. on nylon are not recommended because washing fastness falls below acceptable values for end-use. Published data for this exact dye/fibre configuration is limited; laboratory trials with the target fabric are therefore required before bulk processing.
Competitive Disperse Violet 57 prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: sales3@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Industrial product entries for C.I. Disperse Violet 57 describe an anthraquinonoid disperse colorant standardized primarily for hydrophobic substrates, especially polyester and polyester-cellulosic blends. The commercial range is supplied as aqueous presscake, powder, and non-dusting liquid dispersion. Liquid grade is commonly standardized to 40 % relative strength and is pre-dispersed with naphthalene-sulfonate condensate or lignosulfonate. Powder grade may be offered at 100 % or 200 % relative strength; the certificate of analysis lists active colorant strength, pH of a 1 % aqueous dispersion, moisture, and residue on sieve. Because the C.I. generic name does not define dispersant loading, electrolyte level, or particle-size distribution, incoming inspection should compare the lot against the same supplier reference used for standardization. The dye is not a chemical specification by itself; the molecular formula and CAS registry for the purified colorant are indicated on the supplier’s safety data sheet and vary with the finishing auxiliaries present.
The dye is dispersed in cold demineralized water at 40 °C–50 °C before transfer to the dye bath. A stock dispersion is sieved or filtered to remove agglomerates; high-temperature dispersion stability is assessed by GB/T 5541 or AATCC TM146. The dye bath is set with acetic acid to pH 4.5–5.5; above pH 6.0, alkali hydrolysis can reduce color yield and produce duller, redder residues. The exhaust profile uses a ramp rate of 1.0 °C/min–2.0 °C/min to 130 °C, with a hold of 30 min for pale shades and 45 min–60 min for deep shades. Jet or package dyeing machines with liquor ratios of 1:8 to 1:15 are typical for woven and knitted polyester; package density and pump flow must be balanced to avoid channeling.
Dye uptake is diffusion-controlled under these conditions; apparent exhaustion is depressed by excessive dispersant, high liquor ratio, or fabric preparation residues. A dispersing agent concentration of 1 g/L–2 g/L is maintained, and reducing agents must be absent before fixation. After dyeing, the bath is cooled to 80 °C before overflow rinse. Reduction clearing in alkaline hydrosulfite is normally applied to remove surface dye and improve fastness. Fastness of the resulting dyeings is evaluated by ISO 105-C06:2010, ISO 105-X12:2016, and ISO 105-B02:2014.
For continuous pad–dry–thermofix lines, C.I. Disperse Violet 57 is applied to polyester or polyester/cotton with an anti-migrant and a wetting agent. A pad liquor containing 20 g/L–60 g/L of dye is used for medium depths; pick-up is controlled to 50 %–70 % on a horizontal or vertical padder with even pressure across the fabric face. The fabric is predried at 100 °C–120 °C, then thermofixed in hotflue at 190 °C–210 °C for 60 s–90 s. The upper fixation limit is constrained by sublimation and shade loss. Published data for this specific configuration is limited, so the exact combination of temperature and dwell time should be verified by a thermofixation series on the target fabric. After thermofixation, residue is removed by reduction clearing or alkaline scouring. The process is less forgiving than exhaust dyeing because moisture variations during predrying can create side-to-center shade differences on wide fabric widths. Commercial hotflues with air-temperature control of ±2 °C are preferred; a wider control band can produce visible shade drift on pale depths.
The practical distinction between C.I. Disperse Violet 57 and earlier anthraquinonoid violets is observed in thermal fastness and shade. Low-energy products such as C.I. Disperse Violet 1 (1,4-diaminoanthraquinone) are bright but lose depth through vapor-phase transfer above 180 °C. Chlorine substitution on the anthraquinone nucleus increases relative molecular mass and lowers vapor pressure, so medium-energy products—often handled as C.I. Disperse Violet 28 or C.I. Disperse Violet 57—are retained through thermofixation at 200 °C under controlled dwell. However, the commercial names are not interchangeable: each C.I. designation may differ in the position of substituents, dispersant system, and hue cast. Violet 57 is typically selected where a redder violet build-up is required; Violet 28 may show a bluer cast and different compatibility in ternary combinations.
Fastness ratings under ISO 105-B02:2014 for Xenotest exposure or ISO 105-P01:1993 for sublimation are not intrinsic properties; they depend on dye concentration, substrate denier, heatsetting history, and afterclearing. Anthraquinonoid disperse dyes of this range generally produce better pH stability and chroma than some monoazo high-energy violets but can have lower saturation on microdenier polyester. On microdenier polyester, the apparent depth may require 1.5–2.0 times the dye loading used on regular denier fabric to reach the same visual depth; published data for this specific configuration is limited. This behavior differs from high-energy azo violet products that often build-up economically but may yield duller red-violet tones.
For carrier dyeing at atmospheric boil or below 100 °C, a carrier such as methylnaphthalene or o-phenylphenol is used at 2 g/L–5 g/L. The carrier swells polyester and accelerates diffusion, but it also reduces lightfastness if retained; a post-scouring or hot-air treatment at 140 °C for 15 min–20 min is applied. Disperse Violet 57 can also color secondary acetate and triacetate; triacetate requires a carrier or high-temperature procedure because its compact structure slows diffusion. On acetate, wet fastness is lower than on polyester, and the pH should be maintained at 5.0–6.0 to avoid saponification of the fiber surface. Liquid grades are preferred for carrier dyeing because powder grades may agglomerate when added directly to hot water. Polyamide uptake is possible, but reserve and wet fastness are less favorable; selection on nylon is usually limited to pale shades.
Combination shade matching with Disperse Violet 57 requires compatibility data measured by parallel exhaust trials. The dye is screened with a reference trichromatic set at 1.0 % total depth and at 2.0 % total depth. If the uptake curves diverge, shade stability across the ramp becomes poor; sampling at 110 °C, 120 °C, and 130 °C reveals blocking. This is a common failure mode on package dyeing machines where flow distribution is not uniform. Batch-to-batch variance in dispersant loading can shift apparent depth even when colorant strength is within specification. Transfer printing is not recommended as a primary application for Disperse Violet 57 unless the commercial grade has been milled to D90 < 0.5 µm and the transfer paper is run at 210 °C for 30 s. Inkjet formulations require D99 < 0.2 µm and filtration through 0.45 µm absolute filters. Published data for this specific configuration is limited.
Reduction clearing is a critical aftertreatment for polyester dyed with Disperse Violet 57. A typical clearing bath contains sodium hydrosulfite at 1 g/L–2 g/L and caustic soda to pH 10–11, held at 70 °C–80 °C for 15 min–20 min. The clearing operation removes unfixed surface colorant and improves wash and rubbing fastness; it also changes the final hue by stripping loosely bound dye. Because the colorant is anthraquinonoid, excessive alkaline clearing can hydrolyse the fixed dye and reduce depth. The hydrosulfite bath should be thoroughly rinsed and neutralized with acetic acid. In dyehouse practice, reduction clearing may be omitted for very pale shades or for printing applications where dry-heat fixation has already removed volatiles.
Operational boundaries are explicit: the dye bath must not be set above pH 6.0 during high-temperature dyeing; reducing agents must be absent before fixation; dried dye films should not be exposed to live steam above 140 °C before thermosol fixation. Combination with cationic aftertreatments before clearing can create insoluble complexes and should be avoided. Storage of powder grades above 60 % relative humidity may require pre-drying to prevent strength drift and poor dispersion.
Because Disperse Violet 57 is supplied under multiple commercial models, incoming inspection should be based on the supplier’s certificate of analysis and the methods listed below. The table is a compliance matrix, not a set of absolute acceptance values; limits are product-grade specific.
| Relative strength and shade | GB/T 2394 |
| pH of aqueous dispersion | ISO 787-9 |
| Moisture / volatile content | ISO 760 |
| Particle size distribution | ISO 13320 |
| High-temperature dispersion stability | GB/T 5541 / AATCC TM146 |
| Light fastness on polyester | ISO 105-B02:2014 |
| Wash fastness | ISO 105-C06:2010 |
| Sublimation fastness | ISO 105-P01:1993 |
| Rubbing fastness | ISO 105-X12:2016 |
Liquid dispersion viscosity is evaluated by rotational viscometer under ISO 3219; a supplier-specific acceptance limit for a 40 % concentrate may be set at 500 mPa·s maximum at 25 °C, but this value is not universal. The specification should also indicate residue on 0.076 mm sieve and storage stability. Dyed fabric quality is judged against the end-use fastness matrix; no single standard value applies across all substrates.