| HS Code | 489061 |
| Product Name | Mesophilic Desizing Enzyme |
| Product Type | Amylase enzyme for textile desizing |
| Enzyme Activity | 100,000 U/mL (or specified by batch) |
| Optimum Temperature | 45–60°C |
| Ph Range | 5.5–7.5 |
| Appearance | Light brown to amber liquid |
| Solubility | Fully water-soluble |
| Storage Stability | Stable for 12 months at 4–25°C |
| Packaging | Available in 25 kg, 200 kg, and 1000 kg containers |
| Application | Removes starch-based sizes from fabric under mesophilic conditions |
| Dosage | 0.2–1.0 g/L depending on fabric and desizing conditions |
| Safety Profile | Non-toxic, biodegradable, avoid contact with eyes and skin |
As an accredited Mesophilic Desizing Enzyme factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Mesophilic Desizing Enzyme is packaged in 25 kg sealed fiber drums with inner polyethylene bags, ensuring dry, stable storage. |
| Container Loading (20′ FCL) | 20′ FCL: one container loaded with mesophilic desizing enzyme drums, properly secured, temperature-controlled, ventilated, and labeled for safe transport. |
| Shipping | Ship mesophilic desizing enzyme in sealed, food-grade containers, protected from moisture and direct sunlight. Maintain temperatures between 5–25°C to preserve activity. Avoid freezing or excessive heat. Label as non-hazardous but use spill-containment during transit. Ensure dry, ventilated storage and immediate use after receipt to maximize shelf life. |
| Storage | Store Mesophilic Desizing Enzyme in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and moisture. Keep the container tightly sealed when not in use to prevent contamination and caking. Avoid storage above 25°C; refrigeration can extend shelf life. Use within the manufacturer’s stated expiry period. |
| Shelf Life | Shelf life is typically 6 months when stored cool, dry, and away from direct sunlight. |
In continuous open-width preparation of woven cotton sheeting intended for alkaline scouring and hydrogen peroxide bleaching, starch-based size films on warp yarns constitute the primary water-insoluble barrier removed before mercerizing. Mesophilic α-amylase applied by pad-batch hydrolyzes the α-1,4-glycosidic linkages in amylose and amylopectin into lower-molecular-weight dextrins that are readily dispersed in the subsequent hot wash. The preferred production route runs at 25–40 °C and pH 5.5–6.5, which avoids the fabric strength loss and oxalate formation associated with high-temperature oxidative desizing on cotton. A horizontal two-bowl or three-bowl padder is set to deliver 70–80% wet pickup on dry fabric weight, and the enzyme concentration is typically 0.3–1.5 g/L in the pad trough along with 0.5–2.0 g/L of a nonionic wetting agent. The padded web is wound on a low-tension A-frame or large-roll batching station and wrapped in polyethylene film; dwell time is held between 6 h and 24 h depending on fabric construction, woven density, and plant temperature. Process control requires that the batch does not form dried edges or condensate drips, because evaporative moisture loss concentrates auxiliary salts and stops enzymatic hydrolysis at the selvedge. Residual starch after washing is checked qualitatively by iodine staining according to AATCC 94-2017; a negative blue-violet response confirms that the size film has been degraded. Chemical inputs for this route are expected to conform to ZDHC MRSL 3.1, hold an OEKO-TEX ECO PASSPORT certification, and appear on approved input lists under GOTS 7.0 when organic cotton is processed. Within the European Union, the formulation is placed on the market under REACH Regulation (EC) No 1907/2006, and the finished textile must satisfy the chemical safety requirements of GB 18401-2010 for Class B products if imported into China. The desizing enzyme is not effective on polyvinyl alcohol, carboxymethyl cellulose, or acrylic copolymer sizes; if mixed synthetic sizes are present, a combined oxidative-enzymatic pad-steam route or a separate oxidative step is required. Baths contaminated with residual hypochlorite from bleach cleaning cycles depress enzyme activity, so separate dosing lines and complete rinsing between oxidative and enzymatic stages are mandatory. Finished terminal articles from this pad-batch desizing route include 100% cotton woven bed sheeting, shirting, table linen, and sateen bed covering.
The jigger treats woven fabric in open width under low liquor ratio, but its discontinuous immersion and squeezing cycle can leave starch residues at the fabric surface if the enzyme contact time is too short or the bath temperature falls below the mesophilic activity window. For yarn-dyed poplin, the operational target is to remove starch without mobilizing unfixed dye or triggering cross-colour staining during the long dwell between ends. The enzyme dosage is set at 0.1–0.5% owf, bath pH is maintained at 6.0–6.8, and the temperature is controlled between 45 °C and 60 °C at a liquor ratio of 1:5–1:8. Treatment time of 30–60 min over multiple jigger passes is sufficient for starch hydrolysis; a nonionic penetrating agent at 0.2–0.5 g/L assists size wet-out on densely sett poplin. After enzyme treatment, the bath is drained and the fabric is washed in a counterflow sequence at 80 °C with a nonionic detergent, followed by cold rinsing. Chemical inputs applied to yarn-dyed goods are screened against ZDHC MRSL 3.1 and OEKO-TEX ECO PASSPORT; finished fabric is evaluated for colour fastness to washing according to ISO 105-C06:2010 and for dimensional change according to ISO 6330:2021 where applicable. The terminal products include yarn-dyed poplin shirting, dobby shirtings, and cotton lining fabrics. If colour bleed is observed, the desizing bath should be buffered below pH 7.0 and the temperature reduced toward the lower end of the recommended interval, because vat and reactive dye desorption from sized yarns increases as pH and temperature rise. The use of open-width jigger machines with variable tension control is preferred; excessive fabric tension during the low-liquor contact stage can set crease marks that remain visible after finishing.
When denim garments arrive at the laundry from cut-and-sew operations, warp yarns carry starch-based sizing that stiffens seams and prevents uniform mechanical abrasion in subsequent stone washing or cellulase treatment. An exhaust-style desizing step in a front-loading washer-extractor removes the starch size before pumice stones or neutral cellulase systems are introduced, and the mesophilic α-amylase operates at 40–60 °C and pH 5.5–7.0. The enzyme dose is 0.2–0.8% owg on garment weight, with a liquor ratio of 1:8–1:12 and a residence time of 15–40 min depending on denim weight and starch add-on. Programmable washer-extractors with reversing intervals of 25–35 rpm are used to achieve mechanical flexing without excessive garment tangling. Denim laundries operating under ZDHC Wastewater Guidelines v2.2 and Bluesign system black limits require desizing formulations free of alkylphenol ethoxylates and phosphates; the enzyme preparation should hold OEKO-TEX ECO PASSPORT certification. The desizing bath should remain below pH 7.5, because higher alkalinity promotes indigo redeposition onto pocket linings and weft yarns; a nonionic anti-redeposition agent at 0.3–0.5 g/L is dosed when washed-down indigo concentration rises. The amylase preparation must be free of cellulase side activity, since even low cellulase contamination can reduce tensile strength before the intended abrasion step. Garment tensile strength retention is monitored by ASTM D5035-11(2019) on construction seams and high-abrasion panels. Terminal garment types include five-pocket jeans, denim jackets, skirts, and shorts; the desizing step is considered complete when the fabric shows no blue-violet colour in an iodine spot test aligned with AATCC 94-2017. Batch-to-batch variation arises mainly from differences in starch add-on from weaving mills, and laundries adjust enzyme dose upward within the stated range for stiff, heavily sized denim while maintaining pH below 7.0 to avoid back staining.
Terry constructions present a high pile density and low ground-warp tension tolerance; starch size is applied to ground and pile warps to survive weaving, but must be removed before bleaching to allow uniform hydrogen peroxide penetration and loop openness. Mesophilic desizing enzyme for terry towel preparation is dosed at 0.3–1.2 g/L in pad-batch or 0.2–0.6% owf in jigger processing, with bath pH held between 5.5 and 6.5 and temperature at 30–45 °C. Pad-batch dwell time ranges from 8 h to 16 h, and the fabric is wrapped in polyethylene film to avoid edge drying. Open-width processing is mandatory because rope-form treatment crushes wet pile loops and creates permanent pile distortion, so low-tension padder and A-frame batching are used before hot wash at 85–95 °C with nonionic detergent. The finished towels for direct skin contact fall under OEKO-TEX Standard 100 Class I criteria; process chemicals must appear on GOTS 7.0 approved input lists when organic cotton is used. Absorbency is assessed by AATCC 79-2018, and residual starch is detected by AATCC 94-2017 before peroxide bleaching. Terminal products include bath towels, bathrobes, beach towels, and kitchen towels. If the batch is allowed to dry or if low-moisture conditions persist in the plant, starch degradation stops before adequate hydrolysis and the subsequent scouring step shows uneven capillary rise; published production-scale data for overdry batch failures in terry mills are limited, but the iodine spot test and AATCC 79-2018 results provide the required release judgement.
| Configuration | Enzyme dosage | pH window | Temperature | Contact time | Critical control limit |
|---|---|---|---|---|---|
| Pad-batch woven cotton sheeting | 0.3–1.5 g/L | 5.5–6.5 | 25–40 °C | 6–24 h | PE wrap to prevent edge drying |
| Jigger yarn-dyed poplin | 0.1–0.5% owf | 6.0–6.8 | 45–60 °C | 30–60 min | Dye bleed below pH 7.0 |
| Denim garment desizing | 0.2–0.8% owg | 5.5–7.0 | 40–60 °C | 15–40 min | Indigo redeposition above pH 7.5 |
| Terry towel preparation | 0.2–0.6% owf | 5.5–6.5 | 30–45 °C | 8–16 h | Pile loop crush in rope processing |
| Heat-set poly/cotton blend | 0.4–1.0 g/L | 5.5–6.5 | 40–50 °C | 8–16 h | Incomplete wet-out on polyester |
| Reactive print cloth pretreatment | 0.5–1.5 g/L | 5.5–6.0 | 30–40 °C | 12–24 h | Persistent iodine blue response |
Polyester–cotton blends that have passed through a tenter heat-setting stage develop a less swellable polyester phase; residual starch on the cotton component is physically less accessible to water and enzymatic cleavage, yet strong oxidative desizing introduces alkali-induced ester hydrolysis risk to the polyester component. Mesophilic α-amylase removes starch size without the fiber swelling and alkali damage associated with hydrogen peroxide or sodium hydroxide intensive systems. For pad-batch application on heat-set poly/cotton workwear twill, the enzyme is dosed at 0.4–1.0 g/L, pH is maintained at 5.5–6.5, temperature is held at 40–50 °C, and dwell time is 8–16 h with wet pickup of 65–75%. A nonionic wetting agent is added at 0.5–1.0 g/L to improve size wet-out on the hydrophobic polyester fraction; low-tension padder deflection rolls prevent crease formation on heat-set fabric. After enzyme batching, the fabric is washed at 80 °C with sequestrant-free detergent, since calcium-binding agents can destabilize residual enzyme and create uneven desizing at the interface between cotton and polyester. Workwear and uniform fabrics imported into the European Union require conformity with REACH Regulation (EC) No 1907/2006 Annex XVII; chemical inputs should meet ZDHC MRSL 3.1 and OEKO-TEX ECO PASSPORT. The enzyme will not remove polyvinyl alcohol, polyester size, or waxes carried over from spinning; if the size mix contains PVA or CMC, a separate oxidative desizing or size-respecific blend is required. Terminal articles include poly/cotton workwear, uniforms, bed sheeting, and pillow ticking. Published mill data on enzyme diffusion into heat-set blend interfaces are limited; therefore a plant validation using AATCC 94-2017 and AATCC 79-2018 is recommended before bulk production.
Residual starch on cotton print cloth before rotary screen printing reacts with reactive dyes during steaming, lowering colour yield and producing uneven ground colour after washing. A mesophilic α-amylase pad-batch step before alkaline scouring hydrolyzes starch into water-extractable dextrins that are removed prior to alkali treatment, preventing starch–reactive dye adduct formation in the print paste. The enzyme is applied at 0.5–1.5 g/L, pH 5.5–6.0, temperature 30–40 °C, and wet pickup 70–80%, with batching time of 12–24 h. After batching, the fabric is washed at 85 °C with nonionic detergent and then checked for residual starch by iodine spot test according to AATCC 94-2017; if a blue-violet colour persists, the batch is extended or the fabric is reprocessed before scouring. Chemical inputs and pretreated fabric should conform to GOTS 7.0 where organic cotton is used; finished printed textiles must meet OEKO-TEX Standard 100 Class I or Class II depending on end use, and colour fastness to washing is assessed by ISO 105-C06:2010. The critical pH limit is 5.0; below this value enzyme activity falls and the acid can hydrolyze cellulose over long batch times, while above 6.5 the mesophilic amylase stability drops and residual starch may survive. Terminal printed articles include rotary screen printed cotton apparel fabric, printed bed linen, table linen, and decorative textile. Because reactive print cloth is often mercerized after desizing, complete starch removal also prevents caramelized starch deposits on mercerizing rolls and subsequent colour specks in the print ground.
Competitive Mesophilic Desizing Enzyme 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 admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Mesophilic Desizing Enzyme MDE-40L is a liquid bacterial alpha-amylase preparation derived from a non-pathogenic Bacillus strain. The enzyme catalyses random hydrolysis of α-1,4-glycosidic bonds in gelatinised starch size, reducing high-molecular-weight amylose and amylopectin to water-soluble dextrins and maltodextrins. The preparation is standardised to a declared activity of 40,000 U/g, where one unit releases 1 μmol of reducing sugar, expressed as maltose, per minute at 40 °C and pH 6.0 under a DNS reducing-sugar assay. The product is classified under EC 3.2.1.1 and is supplied as an amber liquid with slight haze.
| Property | Method | Specification |
|---|---|---|
| Declared activity | DNS reducing-sugar assay, 40 °C, pH 6.0 | 40,000 U/g representative; lot-specific value on certificate |
| Density at 20 °C | ASTM D4052-22 | 1.05–1.15 g/cm³ |
| pH | Potentiometric, 25 °C | 5.5–7.0 |
| Viscosity at 25 °C | Brookfield LV, spindle 2, 60 rpm | < 2,000 mPa·s |
| Appearance | Visual inspection | Amber liquid, slight haze |
Starch size hydrolysis proceeds through internal cleavage of the starch chain. High-molecular-weight fractions are converted to water-soluble dextrins, which are removed by rinsing. Because desizing efficiency depends on starch swelling and enzyme accessibility, the pad bath must be maintained at a temperature that permits partial gelatinisation of the applied size. The gelatinisation boundary for native maize starch is reported near 62–72 °C, but steam-slackened or thin-boiling starch sizes used in weaving may swell at lower temperatures. Mesophilic operating conditions therefore trade lower thermal energy for longer hold time and require close control of bath pH and metal-ion availability.
Continuous padder–J-box or pad-batch ranges require simultaneous control of wet pickup, enzyme activity retention, and holding time. Woven cotton with starch add-on of 8–12 % is padded to 70–90 % wet pickup; mangle pressure is adjusted so that the liquor covers the size without excessive dripping. The working bath is held at 50–60 °C, pH 5.5–7.0, with 0.5–1.0 g/L nonionic wetter. Enzyme dose is normally 1.0–2.0 g/L for heavily sized fabrics. Fabric entering the J-box should not exceed 70 °C; if the temperature exceeds 75 °C for longer than 20 min, measurable activity loss occurs and residual starch is elevated. The padded roll is covered with polyethylene film or the J-box is sealed to prevent drying, and the batch is held for 8–24 h. At the exit, residual starch is checked by iodine stain per AATCC TM81; a trace yellow response is the control limit. A pH shift below 5.0, often caused by acidic softeners or acid-steeping carryover, is a more common cause of failure than modest temperature drift.
Exhaustion desizing in jet or overflow equipment is run at liquor ratios between 1:5 and 1:10. The bath is set at 50–60 °C and the enzyme is dosed at 0.5–2.0 g/L after the machine reaches temperature. A 15–30 min holding period after loading is sufficient for starch removal on light- and medium-sized knits; heavy woven constructions may require 30–45 min. Foam from starch hydrolysate can depress circulation pump efficiency in high-shear jet machines; defoamers used must be enzyme-compatible. Antifoam emulsions based on mineral oil or hydrophobic silica are not automatically compatible; a screening test in the intended bath is required. High anionic surfactant concentrations from upstream scouring should be rinsed to below detectable foam persistence before enzyme addition.
Calcium ions stabilise the tertiary structure of bacterial alpha-amylase. In soft water, the product retains activity, but if ion-exchange softening is combined with strong chelators such as EDTA, NTA, or sodium tripolyphosphate, free calcium can fall below 20 mg/L. Under those conditions, desizing rate falls and residual starch may appear at the end of the batching period. The corrective action is to add 0.1–0.3 g/L calcium chloride dihydrate to the pad bath or exhaustion bath and verify free calcium by titration or ion-selective electrode. Heavy metals such as iron, copper, and zinc are inhibitory at concentrations above 1 mg/L and should be removed by water treatment before the enzyme bath is prepared. Sequestering agents that preferentially bind divalent ions must not be used unless the supplier has confirmed a calcium-independent formulation.
The product does not hydrolyse polyvinyl alcohol, carboxymethyl cellulose, or acrylate sizes. When mixed starch/PVA sizes are present, a single enzyme stage removes the starch component and reduces the overall size film integrity, but the synthetic fraction remains as a residual film unless an oxidative or hot alkaline scouring stage follows. This distinction is critical for fabric that must meet water absorbency and dye uptake uniformity tests such as AATCC TM79 or a drop absorbency method. The enzyme is appropriate for starch or starch-rich blends; for PVA-dominant size, oxidative desizing is more appropriate.
Process water with high conductivity from sodium chloride or sodium sulfate does not inactivate the enzyme at concentrations commonly encountered in dyehouse recycling, but concentrated brine above 50 g/L should be avoided because salt-induced protein aggregation may occur. Nonionic wetting agents at 0.5–1.0 g/L are compatible; anionic surfactants such as dodecylbenzenesulfonate can be inhibitory at high concentrations, particularly in the presence of low calcium. Cationic surfactants and quaternary ammonium sanitizers are not compatible and must be rinsed from storage tanks and dosing lines. Foaming is controlled by mechanical deaeration or by a compatibility-tested defoamer.
Differentiation from high-temperature alpha-amylase rests primarily on the inactivation boundary. A thermostable bacterial amylase is usually applied at 80–95 °C and tolerates short excursions to 105 °C, permitting pad-steam ranges where gelatinisation and enzymatic hydrolysis occur in the steam chamber. The mesophilic product is not suitable for that condition; its continuous exposure ceiling is 70 °C, and irreversible denaturation accelerates above 75 °C. The lower operating temperature reduces energy demand and lowers the risk of yellowing heat-sensitive cellulosics or elastane blends. Published data comparing total energy consumption for this specific product configuration is limited.
| Parameter | Mesophilic Desizing Enzyme | High-Temperature Alpha-Amylase | Oxidative Desizing Agent |
|---|---|---|---|
| Active chemistry | Bacterial alpha-amylase | Thermostable alpha-amylase | Persulfate or alkaline peroxide |
| Typical operating window | 50–70 °C, pH 5.5–7.0 | 80–95 °C, pH 6.0–7.5 | 90–100 °C, alkaline pH |
| Starch removal mechanism | Hydrolysis of α-1,4-glycosidic bonds | Hydrolysis of α-1,4-glycosidic bonds | Oxidative chain scission |
| Calcium dependence | Moderate; maintain free Ca2+ > 20 mg/L | High; often requires Ca2+ plus stabiliser | Not applicable |
| Residual starch test | AATCC TM81 iodine stain | AATCC TM81 iodine stain | AATCC TM81 or weight loss |
| Primary limitation | Inactivation above 75 °C | Higher energy input | Fibre damage risk; no temperature limitation |
Compared with oxidative desizing using sodium persulfate or alkaline hydrogen peroxide, the enzyme acts without fibre oxidation. It does not generate hydroxyl radicals, which is an advantage for fabric strength retention measured by ASTM D5035-22 strip tensile method, but it also does not remove fats, waxes, pectin, or motes; a separate alkaline scouring stage is necessary. Residual hydrogen peroxide from bleaching carryover must be below 5 mg/L in the enzyme bath. Peroxide oxidises methionine residues in the active site and can be removed by catalase or repeated rinsing. The enzyme is not compatible with hypochlorite or peracetic acid sanitisation residues; dosing lines must be flushed with water before charging the bath.
Store the sealed container at 0–25 °C, away from direct sunlight and humidity. Liquid alpha-amylase preparations are sensitive to repeated freeze-thaw cycles; if freezing occurs, the container should be brought to 20–25 °C and mixed gently before sampling, but activity must be re-verified by the DNS assay if phase separation or precipitation is visible. The manufacturer’s certificate of analysis reports lot-specific activity and bacterial count; containers stored beyond 12 months or above 25 °C should be retested before use. Avoid contamination by water or foreign matter, and use dedicated dosing equipment. Industrial enzyme liquids can act as respiratory sensitisers if mist is generated; engineering controls should include local exhaust ventilation or mist suppression.
Quality control on the production floor is based on residual starch detection and fabric absorbency. A pass is recorded when the iodine stain per AATCC TM81 shows no blue-violet colour at the centre of the fabric and water drop absorbency is achieved within the time target set by the dyehouse. Dye uptake uniformity in subsequent reactive dyeing is monitored by shade consistency, not by enzyme activity alone.