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Tetraacetylethylenediamine

    • Product Name: Tetraacetylethylenediamine
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 986680
    Productname Tetraacetylethylenediamine
    Iupacname N,N,N',N'-tetraacetylethane-1,2-diamine
    Casnumber 10543-57-4
    Ecnumber 234-123-8
    Molecularformula C10H16N2O4
    Molecularweight 228.25 g/mol
    Appearance White to off-white crystalline powder or granules
    Odor Odorless to slight acetic odor
    Meltingpoint 149-152 °C
    Boilingpoint Decomposes before boiling at normal pressure
    Density 1.2-1.3 g/cm³ (relative density)
    Bulkdensity 0.6-0.8 g/cm³ (granular)
    Watersolubility Slightly soluble in water at room temperature
    Ph 6-8 (1% aqueous suspension)
    Flashpoint > 200 °C
    Decompositiontemperature > 200 °C
    Vaporpressure Very low; < 0.01 Pa at 20 °C
    Assay ≥ 98%
    Moisturecontent ≤ 0.5%

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

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    Application of Tetraacetylethylenediamine

    What Molar Ratio Controls Peracetic Acid Generation in Low-Temperature Laundry Powders?

    In heavy-duty laundry detergent powders and tablets, tetraacetylethylenediamine (TAED) is incorporated at 1–6 wt% as a bleach activator for sodium percarbonate or sodium perborate monohydrate, and the perhydrolysis stoichiometry requires 2 mol hydrogen peroxide per 1 mol TAED to release 2 mol peracetic acid with 1 mol N,N′-diacetylethylenediamine as the residual amine. Formulators typically set the sodium percarbonate level at 10–25 wt% so that hydrogen peroxide is in molar excess over TAED, because the competing alkaline hydrolysis of TAED to acetate and N,N′-diacetylethylenediamine becomes significant when the wash-liquor pH exceeds 11.5. The granules are dry-blended into post-spray base powder or compacted in tablet form; segregation between TAED granules and larger percarbonate agglomerates is controlled by matching the sieve cut to 200–800 µm and by using a continuous ploughshare mixer with a chopper speed below 1,500 rpm to avoid attrition. Under IEC 60456:2010 washing-machine test conditions, cotton swatches stained with EMPA 101, EMPA 114, and EMPA 116 are used to evaluate low-temperature bleach activity at 20–40°C; the TAED-perborate system shifts the effective bleaching window downward from conventional hydrogen peroxide bleaches that require above 60°C. The terminal product is a wash liquor containing peracetic acid in the 10–80 mg/L range, depending on TAED loading and wash temperature. TAED-containing detergent powders should be stored below 60% relative humidity, because free moisture above 2 wt% in the finished powder can initiate pre-release of peracetic acid during storage, and TAED should not be dry-blended with strongly acidic additives that would promote premature acetylation transfer.

    Automatic dishwashing tablets expose TAED to a more concentrated alkaline wash solution than laundry, with main-wash pH typically 10.0–11.5 and temperatures of 45–65°C in programmes tested under IEC 60436:2015. TAED loading of 2–5 wt% in tablet cores, combined with 10–20 wt% sodium percarbonate and 20–40 wt% sodium disilicate or sodium citrate builders, generates peracetic acid in the wash liquor at the point where bleachable tea, coffee, and polyphenolic residues have softened but not yet redeposited on glass and stainless steel. Multi-layer and core-in-shell tablet presses operating at compaction forces between 15 and 50 kN separate TAED from hygroscopic percarbonate or acidic rinse-aid cores, because direct contact with free moisture at the granule interface initiates premature effervescence. If TAED granules are milled below 100 µm, dust formation increases and the perhydrolysis reaction in the main-wash peak can release peracetic acid as a burst that is partly lost before the soil has been fully wetted; if the granules exceed 1,000 µm, dissolution may be incomplete during the 15–30 min main-wash cycle. The terminal product is a tablet that delivers peracetic acid in the range 50–200 mg/L in the main-wash liquor, depending on water hardness and programme duration.

    Process segmentTAED loadingPeroxide sourceWorking pHTemperature
    Laundry powder1–6 wt%Sodium percarbonate 10–25 wt%9.5–11.020–60°C
    Automatic dishwashing2–5 wt%Sodium percarbonate 10–20 wt%10.0–11.545–65°C
    Pulp brightening0.5–2.0 wt% on oven-dried pulpH2O2 2–4 wt% on o.d. pulp10.5–11.570–90°C
    Textile pad-batch bleaching1–2 g/LH2O2 10–20 g/L as 50% active11–1225–30°C

    Hard-Surface Disinfection Compliance and Precursor Loading under EU BPR

    The biocidal use of in situ generated peracetic acid from TAED in hard-surface disinfectants is regulated under EU Biocidal Products Regulation No 528/2012, where the generated peracetic acid is considered the active substance released from the TAED precursor. A typical ready-to-use disinfectant solution is prepared by dissolving a powder or tablet containing TAED and sodium percarbonate in water at 20–40°C to yield peracetic acid at 100–500 mg/L at pH 7.0–9.5; the solution then acts on pre-cleaned surfaces over a contact time of 5–15 min. Bactericidal activity is tested according to EN 1276:2019 under dirty conditions containing 0.3 g/L bovine albumin, and yeasticidal/fungicidal activity according to EN 1650:2019; sporicidal claims require EN 13704:2019 with additional contact-time validation. Because the TAED-percarbonate system is alkaline during the first dissolution phase, dosing equipment with backflow prevention and corrosion-resistant stainless steel or PVDF wetted parts is specified; prolonged contact with aluminium, brass, or galvanised surfaces can produce alkaline corrosion before the peracetic acid concentration has reached the target. The operational boundary is that TAED dissolution below 20°C is incomplete, and water hardness above 350 mg/L as calcium carbonate can precipitate bicarbonate salts that depress peracetic acid yield. The terminal product is a ready-to-use disinfectant solution that must be consumed within 8 h after mixing because peracetic acid generated in situ decomposes with a half-life that shortens as pH rises above 9.5. Published data for TAED-specific half-life values in this exact ready-to-use configuration is limited.

    When TAED Is Evaluated in Hydrogen Peroxide Brightening of Mechanical Pulp

    When TAED is evaluated as an activator for alkaline hydrogen peroxide brightening of mechanical pulp, the objective shifts from detergency to the oxidation of chromophoric lignin fragments and the controlled removal of carbonyl groups that cause brightness reversion. In a medium-consistency brightening or deinking line at 10–12% stock consistency, TAED is added at 0.5–2.0 wt% on oven-dried pulp with 2–4 wt% hydrogen peroxide, sodium hydroxide, and sodium silicate at pH 10.5–11.5. Retention times of 60–120 min at 70–90°C permit in situ peracetic acid to attack quinoid structures and residual extractives without storing stabilised peracetic acid at the mill. Brightness response is reported as ISO brightness according to ISO 2470-1:2016, and delignification in chemical pulp is tracked by Kappa number according to ISO 302:2004. Operators should cap peracetic acid concentration below 0.2% on oven-dried pulp because higher levels can reduce intrinsic viscosity through cellulose chain scission; published data for softwood kraft pulp under this specific TAED configuration is limited. The terminal product is bleached mechanical or chemical pulp suitable for papermaking grades that require controlled residual peroxide before entering the paper machine; excessive residual peracetic acid must be removed by catalase treatment or extended dilution to avoid interference with cationic retention aids.

    Continuous Textile Bleaching Ranges Demand Rapid TAED Dissolution at Low Bath Ratios

    Continuous knit and woven fabric preparation ranges utilise TAED in peroxide bleaching baths at 1–2 g/L when the target is low-temperature bleaching of cotton and cotton-rich substrates. In a typical pad-batch configuration, the fabric passes through a pad mangle at wet pick-up 80–100%, carrying hydrogen peroxide at 10–20 g/L of 50% active peroxide, caustic soda to pH 11–12, and TAED predispersed in a side tank at 30–40°C with mechanical agitation. The batched roll is stored for 12–16 h at 25–30°C, or steamed for 5–10 min at 100°C in a pad-steam range. Fabric whiteness is evaluated with ISO 11475:2017, and residual peroxide is titrated before dyeing to avoid oxidative destruction of reactive dye chromophores. TAED granules that are not fully dissolved produce localised peracetic acid concentrations on the fabric surface, causing visible white spots; filtration of the pad trough through 100 µm mesh and a minimum liquor ratio of 1:10 reduce this risk. The terminal product is a bleached cotton fabric with a whiteness index suitable for white dyeing or optical brightening, provided the fabric is rinsed below 40°C to prevent alkali-driven strength loss in subsequent tumbling and open-width washing.

    SegmentStandard or regulationMeasured parameter
    LaundryIEC 60456:2010Washing performance and bleach activity on EMPA soiled swatches
    Automatic dishwashingIEC 60436:2015Cleaning performance, soil removal, and programme temperature
    Hard-surface disinfectionEN 1276:2019, EN 1650:2019, EN 13704:2019Bactericidal, yeasticidal/fungicidal, and sporicidal activity
    PulpISO 2470-1:2016, ISO 302:2004ISO brightness and Kappa number
    TextileISO 11475:2017CIE whiteness

    Denture cleanser tablets and alkaline peroxide cleaning sachets require completely dissolving TAED agglomerates in water at 35–45°C to release peracetic acid inside the acrylic surface layer, where oxygen generation and organic stain oxidation coincide. Typical tablet cores contain TAED at 5–10 wt%, sodium percarbonate at 20–40 wt%, citric acid or malic acid at 10–20 wt%, and sodium bicarbonate to produce effervescence; the effervescent disruption of the tablet shortens the dissolution window to 3–5 min, after which the soak time is 15–30 min or overnight for heavy stain deposits. Antimicrobial performance on oral acrylic test coupons can be screened with EN 1276:2019 adapted to denture base materials; published data for TAED-specific denture cleanser formulations under this protocol is limited. Water above 60°C accelerates peracetic acid decomposition and should be avoided; silicone soft liners and metal clasps on removable partial dentures may tolerate only short exposure because the oxidative environment accelerates surface pitting. The terminal product is a soaked, rinsed denture with reduced stain and plaque biofilm, provided the rinse step is completed to remove residual peracetic acid and effervescent salts from the acrylic resin surface.

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