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Direct Deep Brown MM

    • Product Name: Direct Deep Brown MM
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales3@liwei-chem.com
    • Manufacturer: Nanjing Color Science Co.,Ltd
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    Specifications
    HS Code 856411
    Productname Direct Deep Brown MM
    Productcategory Direct dye
    Ci Name Direct Brown 2
    Ci Number 22311
    Chemicalclass Disazo direct dye
    Colorshade Deep brown
    Physicalform Powder
    Watersolubility Soluble in water
    Ioniccharacter Anionic
    Suitablefibers Cotton, viscose, silk, wool, paper, leather
    Dyeingmethod Exhaust dyeing
    Typicaldyeingtemperature 80-95 °C
    Electrolyterequirement Sodium chloride or sodium sulfate
    Ph Range Neutral to slightly alkaline (7-9)
    Lightfastness Moderate
    Washingfastness Moderate
    Storageconditions Dry, cool, ventilated area

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

    Packing & Storage
    Packing Direct Deep Brown MM is packed in 25 kg multi-ply paper bags with polyethylene inner liners, palletized and shrink-wrapped.
    Container Loading (20′ FCL) Direct Deep Brown MM is packed in export-grade bags, palletized, secured inside a 20-foot FCL container, and sealed for shipment.
    Shipping Direct Deep Brown MM is typically shipped as a non-hazardous dyestuff in sealed, moisture-resistant, properly labeled containers. Handle in a dry, ventilated area; avoid dust generation. Transport according to the SDS and applicable local/international regulations. Not classified as dangerous goods unless confirmed by supplier documentation.
    Storage Store Direct Deep Brown MM in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and ignition sources. Keep containers tightly closed, clearly labeled, and upright on stable shelving with secondary containment. Separate from oxidizing agents, acids, alkalis, food, feed, and drinking water. Prevent dust generation and follow local regulations and the safety data sheet.
    Shelf Life Shelf life: approximately 24 months when stored in a cool, dry, well-ventilated area away from direct sunlight and moisture.
    Application of Direct Deep Brown MM

    Jet dyeing of scoured and bleached cotton knit fabrics with Direct Deep Brown MM is carried out at a liquor ratio of 1:10 to 1:20. The colorant is pre-dissolved at 85–90°C and filtered through a 5 μm bag filter before being metered into the circulating bath at 0.5–4.0% o.w.f. Sodium sulfate is added in split portions of 10–15 g/L at the start and after 15 min to maintain a linear exhaustion curve without shock adsorption at the fabric surface. Bath temperature is raised to 95–98°C at 1.5°C/min and held for 45–60 min. The dyebath pH is maintained between 7.0 and 8.0 with 0.5–1.0 g/L soda ash, which also aids solubility of the sulfonated chromophore. After rinsing at 60°C for 10 min, the shade is fixed with a cationic formaldehyde-free fixative at 1–3 g/L and 35–40°C for 20–30 min to reduce washdown. Color fastness to washing is verified according to ISO 105-C06:2010 A2S, and wet rubbing is assessed with ISO 105-X12:2016. During stentering of cotton jersey, cylinder temperature is controlled to 110°C and residual moisture to 6–8% to limit anionic dye migration toward the fabric face. The resulting deep brown shades are used in single-jersey apparel, terry towelling, and cotton interlinings. Because direct dyes exhibit moderate lightfastness, articles intended for prolonged outdoor exposure are excluded from this application unless the finished article is rated under ISO 105-B02:2014 at a grade specified by the retailer. Batch-to-batch shade variation in production-scale machines is monitored by measuring K/S at the approved absorption maximum and maintaining a ΔE CMC 2:1 of 0.5 or less against the physical standard.

    Why Is Intermediate Pre-Drying Controlled at 80°C in Pad-Steam Application?

    Continuous padding of bleached cotton twill with Direct Deep Brown MM requires a pad trough concentration of 10–30 g/L and sodium sulfate at 5–15 g/L. The wet pickup is adjusted on the pad mangle to 70–75% using a shore 70 hardness rubber bowl and a line pressure of 3–5 kN across 180 cm width. The critical process window is the first drying zone: cylinder surface temperatures above 110°C drive unbound dye to the fabric face by capillary migration, producing edge-to-center shade deviation that cannot be corrected at the steamer. An infrared pre-dryer set at 60–80°C reduces surface moisture before contact drying by 30%, after which the fabric is heated to 100–105°C for 40–60 s. Fixation is carried out in saturated steam at 102–105°C for 45–90 s; because Direct Deep Brown MM is substantive, the steamer residence time is shorter than for vat dyes, but insufficient dwell time leads to low wet rub fastness. Washing after fixation uses 60–70°C water in 6 compartments with countercurrent flow to remove unfixed dye and salt. The finished woven fabric is used in chambray shirting, pocketing fabric, and dyed canvas for luggage. Published data for this specific configuration is limited; therefore, plant trials must map steamer temperature against residual dye in the wash water and final wet rubbing grade under ISO 105-X12:2016.

    Package dyeing of ring-spun cotton yarns with Direct Deep Brown MM imposes a filtration constraint that is absent in open-width processing. The yarn packages are wound at a density of 0.35–0.40 kg/L on stainless steel tubes and loaded into a vertical spindle dyeing machine with an inside-out flow direction. The pump is operated at 30–50 L/min per kg of yarn to maintain a differential pressure below 0.5 bar; higher differential pressure compacts the yarn layers and produces non-uniform penetration after the first 20 min. The dye is prepared at 85°C and dosed over 15–20 min, followed by sodium sulfate in three equal portions at 5 min intervals to a final concentration of 8–20 g/L. The bath is held at 95–98°C for 50–60 min, then cooled at 2°C/min to 40°C before fixing. Cationic aftertreatment at 1–2% o.w.f. improves wash fastness but increases the risk of cross-sectional dye accumulation if applied above 4.5 pH. The dyed yarn is used for sewing thread, embroidery yarn, tape labels, and crochet structures. Shade consistency is checked on knitted sock panels using ISO 105-C06:2010 and ISO 105-B02:2014. The operational boundary for package dyeing is the load density: beyond 0.42 kg/L, the pressure drop across the package exceeds the pump design point and the shade lacks core-to-surface uniformity.

    When Leather Drum Dyeing Is Run Above 45°C

    Direct Deep Brown MM is applied to chrome-tanned wet-blue and vegetable-tanned crust leather in a stainless steel drum at 0.5–2.0% based on shaved weight. The float is set at 200–250% for wet-blue and 150–200% for crust leather, with water temperature held at 35–45°C. When the drum temperature exceeds 45°C, the dye uptake rate increases sharply and the grain surface becomes over-saturated within the first 15 min, creating a dark surface film that is not fully penetrated into the corium. The drum speed is set between 12–18 rpm with reverse rotation every 5–10 min; open structure drums with axial paddles provide better mechanical action than fully closed drums for a dye of this molecular size. Dye solution is fed through the hollow drum shaft over 30–40 min, followed by formic acid at 0.5–1.5% diluted 1:10 with water and added in three portions to bring the final bath pH to 3.5–3.8. At this pH, fixation occurs and the residual liquor clears. Runnability constraints include the presence of anionic fatliquors: if sulfated or sulfited fatliquors are overdosed above 8%, the dye shares the active sites and exhaustion drops. The dyed leather is used for shoe lining, bookbinding leather, and upholstery not exposed to direct sunlight. Rub fastness is assessed according to ISO 11640:2018 and light fastness by ISO 105-B02:2014; for automotive or full-grain garment leather, published data for this specific configuration is limited and accelerated weathering would be required.

    Wet-End Retention Aid Interactions in Linerboard and Fine-Paper Production

    In paper stock preparation, Direct Deep Brown MM is charged to the machine chest as a 0.5–1.0% aqueous solution at 0.1–1.5% on oven-dry pulp. The anionic sulfonate groups compete with cellulosic fines for the cationic retention polymer; therefore, the addition sequence must place the dye 10–15 min before the retention aid and after alum. Alum dosage of 0.5–2.0% on dry pulp lowers the headbox pH to 4.5–5.5 and improves substantivity, but excess alum shifts the shade toward a yellower hue due to partial lake formation. A cationic polyacrylamide retention aid is applied at 0.01–0.05% on dry pulp; overdosing above 0.07% reverses furnish charge and causes dye loss in the white water, which is visible as brown tinting of the wire pit. Production-scale Fourdrinier experience shows that wet-end dwell time below 15 min before the fan pump reduces first-pass retention and increases two-sidedness. The dyed linerboard, corrugated medium, and fine paper are used for packaging, file folders, and stationery. Compliance for food-contact paper must be established under FDA 21 CFR 176.170 and 176.180; the supplier must confirm whether Direct Deep Brown MM is listed in the applicable clearance and provide migration data. Bleeding of colored paper and board is tested according to EN 646:2019 where the end use involves food contact.

    Surface coloration of tissue and decor paper at the size press introduces Direct Deep Brown MM into a starch or carboxymethylcellulose film rather than into the fiber bulk. The size press solution is prepared at 8–12% solids with oxidized corn starch or low-viscosity CMC, and the dye is added at 5–20 g/L into the cooked starch at 60–70°C. The size press nip pressure is set to achieve a pick-up of 20–40% wet film on dry paper; higher pick-up above 45% causes dryer deposits on the first steam-heated cylinder and brown transfer marking. The sheet enters the after-dryer section at 70–80°C and exits at 4–6% moisture. Because the dye is located at the sheet surface, dry rub resistance is lower than in wet-end colored grades and must be checked with the felt rub method and EN 646:2019 as applicable. Tissue converted to napkins, party decorations, and wrapping tissue uses this process when a bright deep brown shade is required without the slower drainage cycles associated with wet-end coloration. Printability is retained if cationic charge in the starch film is controlled; an excess cationic surface strength above 0.3 meq/g can mottle ink absorption. The operational boundary is low lightfastness: decorated paper intended for window display or long-term exposure should not be produced with Direct Deep Brown MM unless UV absorbers are incorporated into the coating system, and the compatibility of such absorbers with the sulfonated azo chromophore must be verified in advance.

    Application substrateTest method / standardParameter / limitVerification point
    Dyed textilesEN 14362-1:2017Restricted aromatic amines < 30 mg/kgRaw dyed sample before finishing
    Dyed leatherEN ISO 17234-1:2015Restricted aromatic amines < 30 mg/kgFinished leather article
    Cotton knit / wovenISO 105-C06:2010Washing fastness gradeFinished fabric
    Cotton knit / wovenISO 105-X12:2016Wet and dry rubbing gradeFinished fabric
    LeatherISO 11640:2018Rubbing fastness gradeCrust / dyed leather
    Paper and boardFDA 21 CFR 176.170 / 176.180Component clearanceFood-contact article
    Colored paper and boardEN 646:2019Color bleedingPaper / board for food contact
    Textile / leatherISO 105-B02:2014Light fastness gradeEnd-use exposure validation
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    Certification & Compliance
    More Introduction
    This technical profile introduces Direct Deep Brown MM as an anionic direct dye preparation for cellulosic substrates. The product is supplied as a water-soluble brown dye with a manufacturer-specific “MM” designation that does not by itself establish Colour Index classification. The dyestuff builds deep brown shades by hydrogen bonding, van der Waals adsorption, and fibre-surface entrapment rather than by covalent reaction or reductive vatting. As a result, Direct Deep Brown MM processes in a distinct operational class from reactive brown and sulphur brown systems: auxiliary requirements are lower, but wet fastness is more dependent on electrolyte control and cationic aftertreatment.
    Typical supply specifications for Direct Deep Brown MM
    ParameterControl rangeTest method or reference
    AppearanceDark brown homogeneous powderVisual against supplier reference
    pH of 1% aqueous suspension7.0–9.0ISO 787-9:1981
    Moisture content≤ 5.0%ISO 787-2:1981
    Sieve residue≤ 0.5%ISO 787-7:1981
    Colour strength vs reference lot95–105%Supplier internal spectrophotometric method
    Free aromatic amine, where benzidine-derived congener is present≤ 30 mg/kgEN 14362-1:2012

    What Regulatory Restrictions Apply to Benzidine-Derived Congeners of Direct Deep Brown MM?

    Direct dyes produced from benzidine-based diazo components fall within REACH Annex XVII entry 43, which prohibits azo colourants capable of releasing listed carcinogenic aromatic amines above 30 mg/kg in textile or leather articles that come into direct and prolonged skin or oral contact. If a specific lot of Direct Deep Brown MM corresponds to C.I. Direct Brown 2 or contains that chromophore, the certificate of analysis should report free benzidine by EN 14362-1:2012. Finished goods managed under OEKO-TEX Standard 100 or ZDHC MRSL require batch-level verification because shade-correction blends can alter the congener profile. Published data for this specific configuration is limited; therefore, regulatory status should not be assumed from the trade name alone.

    Dyeing Bath Parameters for Package Exhaust and Jigger Processing

    In package dyeing machines operating at liquor ratios of 1:5 to 1:8, Direct Deep Brown MM is introduced as a filtered stock solution. Dry powder is pasted with demineralised water at a dye-to-water mass ratio of 1:10 and then diluted at 60–80 °C before passing through a 100-mesh screen. Bath pH is maintained at 7.5–8.5 with 1.0–2.0 g/L sodium bicarbonate or a non-volatile buffering agent. Hard water containing more than 150 ppm CaCO₃ is treated with a polyphosphate or polyacrylate sequestrant to reduce dye aggregation and package channelling. For exhaust application of deep shades, the bath is initially set at 40 °C, and dissolved dye is dosed over 10–15 min. Sodium sulphate is added in two portions: 30% of total electrolyte at 60 °C and the remaining 70% at 80 °C. The temperature is then raised to 95 °C at 1.5 °C/min and held for 30–45 min. Circulation in package machines is reversed every 2–3 min because unidirectional flow on soft-wound packages can produce inner-to-outer depth variation of 5–10%. On jiggers operating at 1:2 to 1:4 liquor ratio, electrolyte is added at both ends in equal increments; otherwise concentration gradients across the trough create listing or end-to-end shade differences. Electrolyte sensitivity is the principal control variable for Direct Deep Brown MM. At 2.0% owf dye on bleached cotton knit, raising sodium sulphate concentration from 5 g/L to 20 g/L typically shifts exhaustion from approximately 50% to 80%, but the response flattens above 20 g/L. At 25 g/L and above, aggregation of the anionic dye in high-ionic-strength baths can increase surface deposition and reduce dry-rub performance. Production dyeing therefore requires a defined salt-addition curve rather than a fixed maximum salt concentration. In automated colour kitchens, high-ionic-strength stock solutions should not be held for more than 6 h at 60 °C because slow degradation of standardising diluents can shift viscosity and generate reducing conditions that alter the brown hue. For repeat lot matching, dry dye mass is corrected by spectrophotometric strength. A strength variance of ±3% can correspond to approximately 0.3–0.5 CIELAB Delta E units in a 2.0% owf deep brown shade. On continuous pad-steam ranges for woven cotton or viscose, the padding bath typically contains 20–40 g/L Direct Deep Brown MM, 5–10 g/L nonionic wetting agent, and 10–20 g/L urea. Wet pickup is held at 65–75%, followed by drying to 8–10% residual moisture and passage through a sodium sulphate bath at 50–100 g/L before steaming at 100–102 °C for 45–90 s. Drying below 5% residual moisture promotes dye migration to fabric surfaces and creates selvedge-to-centre depth variation on wide-width goods.

    When Cationic Fixation Is Applied After an Acidic Rinse at pH 5.0–6.0

    Wet fastness limitations are managed by aftertreatment with a cationic fixing agent, but the anionic dyestuff and cationic fixative cannot be present in the same bath. Direct Deep Brown MM at 20–30 °C forms an insoluble stoichiometric complex with quaternary ammonium fixatives, dicyandiamide-formaldehyde condensates, and polyamine derivatives; the complex deposits on the fibre surface as a dull, redder film and blocks package circulation. The standard sequence therefore comprises dyeing at 95 °C, cooling to 70 °C, overflow rinsing, an acid rinse with 0.5–1.0 g/L acetic acid for 10 min, and fresh-bath fixation at 60–70 °C. A deep shade of 2.0% owf Direct Deep Brown MM on cotton is typically rated at grade 2–3 under ISO 105-C06:2010 washing test A1S before fixation. Cationic fixation at 2–4% owf commonly raises the washing fastness to grade 3–4, while dry rubbing fastness under ISO 105-X12:2016 remains at grade 3–4. Overdosing the fixer above 4% owf can reduce light fastness and stiffen the handle. End uses exposed to sunlight should be verified to ISO 105-B02:2014 where a minimum grade of 4 is required.

    Benchmarking Direct Deep Brown MM Against Reactive and Sulphur Brown Systems

    The processing profile of Direct Deep Brown MM differs from reactive brown and sulphur brown systems in auxiliary chemistry, effluent loading, and attainable wet fastness. Reactive brown dyes require covalent alkali fixation and 40–80 g/L electrolyte, whereas sulphur brown dyes require sodium sulphide or a sulphide-free reducing agent and are applied at 70–90 °C. Direct Deep Brown MM operates at 80–95 °C with 5–20 g/L sodium sulphate and no reducing system.
    Comparative processing and fastness characteristics for deep brown shades on cotton
    ParameterDirect Deep Brown MMReactive brown systemsSulphur brown systems
    Application temperature80–95 °C60–80 °C70–90 °C
    Salt requirement5–20 g/L sodium sulphate40–80 g/L sodium sulphate or chloride20–40 g/L sodium sulphate plus reducing agent
    Wash fastness before aftertreatmentGrade 2–3 per ISO 105-C06:2010Grade 4–5Grade 4
    Wash fastness after cationic fixerGrade 3–4 per ISO 105-C06:2010Not usually requiredNot usually required
    Dry rubbing fastnessGrade 3–4 per ISO 105-X12:2016Grade 4–5Grade 4
    Main processing hazardAggregation with hard water and cationic auxiliariesHydrolysis of reactive group and high salt effluentSulphide release, odour, and effluent toxicity
    For leather drum application, Direct Deep Brown MM is added to wet-blue or retanned stock at 55–60 °C and 1.0–3.0% by shaved weight. Penetration improves when the stock is neutralised to a cut pH of 5.0–5.5 before dyeing. Strong acid floats below 4.5 reduce uptake and may produce uneven grain colour. The product is not a metal-complex acid brown, and its light fastness on leather is lower than that of chromium-complex browns. Upholstery leather exposed to UV should be tested to ISO 105-B02:2014 with a minimum grade of 4 before specification. In paper furnish, Direct Deep Brown MM can be metered at 0.2–1.0% on dry fibre at the pulper or fan pump. Wet bleed during sheet formation is controlled by internal sizing; rosin-alum or alkyl ketene dimer sizing evaluated to ISO 535:2014 water absorbency is used when the coloured paper is intended for packaging with incidental water contact. Storage of Direct Deep Brown MM should be maintained below 35 °C and 60% relative humidity to prevent moisture uptake and lump formation. The dye is incompatible with cationic retention aids, cationic fixatives, and amine-functional levelling agents in the same preparation vessel. If a machine changes from cationic to anionic chemistry, an overflow rinse followed by 0.5 g/L sodium carbonate at 70 °C for 10 min is required before introducing Direct Deep Brown MM. Residual sodium hydrosulphite or sodium sulphide from previous vat or sulphur dye cycles must also be removed; reducing conditions cleave the azo chromophore and produce a poor-strength brown shade. No food, drug, or cosmetic contact use should be assumed from this technical profile; food-contact packaging requires separate compliance verification under applicable FDA 21 CFR or EU 1935/2004 conditions.