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Triethyl Acetyl Citrate

    • Product Name Triethyl Acetyl Citrate
    • Alias TEAC
    • Einecs 205-776-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    823497

    Cas Number 77-89-4
    Molecular Formula C14H24O8
    Molecular Weight 320.33 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Slight characteristic odor
    Boiling Point 169°C at 0.1 mmHg
    Density 1.14 g/cm³ at 20°C
    Solubility In Water Slightly soluble
    Refractive Index 1.430 - 1.438 at 20°C
    Flash Point 188°C
    Purity ≥ 99% (commonly)
    Melting Point -20°C
    Ph 1 Solution Approx. 4.5 - 5.5
    Viscosity Approx. 22 mPa·s at 20°C

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

    Packing & Storage
    Packing Triethyl Acetyl Citrate is packaged in a 25 kg blue HDPE drum with secure sealing and clear product and hazard labeling.
    Shipping Triethyl Acetyl Citrate is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It should be stored in a cool, dry, well-ventilated area, away from heat and incompatible substances. Proper labeling, handling with gloves and goggles, and compliance with transport regulations are essential for safe shipping and storage.
    Storage Triethyl acetyl citrate should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Keep it away from heat, sources of ignition, and direct sunlight. Storage temperature should be controlled, ideally at room temperature. Protect from moisture and incompatible substances such as strong oxidizing agents to maintain chemical stability and prevent degradation.
    Application of Triethyl Acetyl Citrate

    Applications of Triethyl Acetyl Citrate in Industrial Manufacturing

    Triethyl Acetyl Citrate serves as a specialized plasticizing, film-forming, and processing aid ingredient across several industrial manufacturing chains. Its performance characteristics address key requirements in strict regulatory environments, supporting downstream producers in delivering compliant, high-quality finished goods.

    1. Pharmaceutical Tablet and Capsule Coating

    Pharmaceutical manufacturers select Triethyl Acetyl Citrate as a plasticizer for enteric and sustained-release film coatings. It supports stable film formation with cellulose and methacrylic polymer systems, minimizing migration while withstanding diverse granulation, coating, and drying conditions. Producers must validate each batch under pharmacopoeial and GMP oversight, ensuring compliance with migration, residual solvent, and extractables limits. The plasticizer enters the formulation during aqueous or organic film coating solution preparation and maintains integrity through spray application and controlled drying. Finished products include oral tablets, caplets, and hard/soft capsules requiring delayed or sustained drug release, as well as sugar- or polymer-coated mini-tablets used for pediatric and geriatric dosage forms.

    Industry compliance standards

    • USP-NF, Ph. Eur., JP pharmacopoeia monographs
    • 21 CFR 172.515 (US FDA indirect food additives for use in pharmaceuticals)
    • ICH Q7 GMP guidelines for active pharmaceutical ingredient (API) manufacturing
    • EU Regulation (EC) No 1333/2008 (for pharmaceutical excipients)

    Typical usage ratio

    • 10–25% by weight in the polymer film-coating mixture,
    • Adjusted based on polymer type, target flexibility, and disintegration profile.

    Downstream process integration

    • Added to coating suspension before homogenization and filtration,
    • Dispersed with polymers and pigments for pan or fluid bed spray application.

    Final product types

    • Modified-release tablets and caplets
    • Gastro-resistant oral dosage forms
    • Sustained- and delayed-release capsules
    • Multiparticulate beadlets for sachets or capsules

    2. Food Contact Flexible Packaging Manufacturing

    Producers in the flexible packaging sector utilize Triethyl Acetyl Citrate as a non-phthalate plasticizer in polyvinyl chloride (PVC) and other film formulations that must comply with direct food contact safety. The molecule reduces film brittleness and improves handling at low temperatures without compromising extractables or organoleptic properties. It enters extrusion or calendaring lines during resin compounding, offering thermal stability under repeated sterilization cycles. Packaging engineers fine-tune levels to balance mechanical properties and migration limits. Finished rolls and preformed pouches serve for dairy, ready-to-eat meals, and fatty food packaging.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on plastic materials and articles intended to contact food
    • US FDA 21 CFR 177.1200 (cellulosic plastics) and 21 CFR 181.27
    • GB 9685-2016 (China food-contact additives)
    • REACH (EC) No 1907/2006 Substances of Very High Concern (SVHC) screening

    Typical usage ratio

    • 15–40 phr (parts per hundred resin) in PVC formulation,
    • Range adjusted to resin grade, desired tensile properties, and regulatory migration testing outcomes.

    Downstream process integration

    • Metered addition to PVC resin before plastisol blending,
    • Integrated into pelletizing, extrusion, or calendering lines before film casting or blowing.

    Final product types

    • PVC-based food wrap and cling films
    • Thermoformable trays for pre-packaged foods
    • Flexible vacuum packaging for dairy, meat, or bakery items
    • Lidding films and pouch laminate structures

    3. Cosmetic Nail Polish Formulation

    Nail polish producers incorporate Triethyl Acetyl Citrate as a phthalate-free plasticizer to enhance film flexibility and gloss while adhering to restrictive fragrance, safety, and allergen standards. Formulators select this additive for its compatibility with cellulose acetate butyrate and nitrocellulose, producing high-performance polishes free of DBP, toluene, or formaldehyde. It enters the compounding process with resins and solvents and stays stable through mixing, quality control, and bottling. The final product addresses consumer demand for safer, longer-lasting nail color and topcoat products for professional and retail markets.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009—Annex II and III
    • US FDA Voluntary Cosmetic Registration Program (VCRP)
    • China National Medical Products Administration (NMPA) cosmetics safety inventory
    • IFRA standards for allergen testing and fragrance load

    Typical usage ratio

    • 8–20% by weight in nail lacquer base,
    • Ratio determined by film flexibility, drying speed, and hardness requirements.

    Downstream process integration

    • Charged with main lacquer resin into solvent blend tank,
    • Homogenized with pigments, flow modifiers, and stabilizers before end-filtration and filling.

    Final product types

    • Color nail enamels
    • Base coats and strengthening treatments
    • High-gloss topcoats
    • Special effect polishes (e.g., glitter, matte, pearlized)

    4. Chewing Gum and Confectionery Softener

    Confectionery manufacturing plants add Triethyl Acetyl Citrate as a food-grade plasticizer and softening agent in chewing gum base and various sugar confection recipes. It improves machinability, texture, and chew retention without contributing flavor or off-notes, and supports low-migration standards for sensitive consumer groups. The raw material is incorporated during the fusion of gum base or starch syrup mixture preparation, providing uniformity across aerated or layered processes. Finished confectionery forms include chewing gum slabs, pellets, dragée centers, and soft pastilles for export and domestic sales.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius GSFA food additive standard 1108
    • EU Regulation (EC) No 1333/2008, Annex II, Group I EC No. E1505
    • US FDA 21 CFR 172.515 (Generally Recognized as Safe—GRAS flavoring and adjuvant)
    • China GB 2760-2014 National Food Safety Standard—Food Additive Use

    Typical usage ratio

    • 0.2–2% by weight of gum base or total confectionery mass,
    • Modulated based on elastic properties, sugar vs. sugar-free recipes, and target texture.

    Downstream process integration

    • Dispersed into molten gum base before incorporation of sweeteners and active ingredients,
    • Added in the liquefaction step for aerated gels, pastilles, or layered bars.

    Final product types

    • Sugar and sugar-free chewing gum—slabs, tabs, centers
    • Elasticated fruit chews
    • Coated and filled pastilles or jellies
    • Functional chewing gums (enriched with active components)

    5. Medical Device Polymer Modifier

    Manufacturers of single-use and short-term implantable medical devices, such as tubing, connectors, and catheters, employ Triethyl Acetyl Citrate as a biocompatible plasticizer in soft PVC, polyurethane, and related polymers. It ensures flexibility, kink resistance, and compatibility with sterilization (ethylene oxide, steam, gamma irradiation) while meeting demanding extractables and leachables profiles. Integration occurs during polymer melt compounding or solvent dissolution, followed by extrusion, injection molding, or blow molding into final forms. End products address specific clinical needs without introducing phthalate-related safety concerns for patients.

    Industry compliance standards

    • ISO 10993 biocompatibility series
    • USP Class VI biological reactivity
    • European Pharmacopoeia 3.1.1, 3.1.6 for plasticized materials
    • FDA 21 CFR 881 and 880 (device plasticizers)

    Typical usage ratio

    • 18–40 phr with PVC resin,
    • Adjusted for required hardness (Shore A/B), transparency, and physical strength for the device class.

    Downstream process integration

    • Pre-mixed with polymer resin and stabilizers,
    • Processed via extrusion or molding under medical cleanroom conditions with in-process QC monitoring.

    Final product types

    • Intravenous and infusion tubing
    • Blood bags (short-term use)
    • Catheters and surgical drainage components
    • Infant care and neonatal tubing devices

    6. Specialty Ink and Coating Additive for Food Packaging

    Printing ink and specialty coating manufacturers use Triethyl Acetyl Citrate as a plasticizer and flow modifier in formulations for food-contact approved inks and coatings, especially for flexible packaging, shrink sleeves, and closures. It enhances printability and adhesion while allowing films to withstand flex-cracking, retort, and freezing. The additive is incorporated during pre-mix of resins and solvents and remains compatible with high-speed gravure or flexographic application systems. Downstream QC verifies migration and organoleptic neutrality before converting rolls or sheets. Finished items include printed wraps for confectionery, snacks, dairy, and beverage shrink sleeves with regulatory declarations.

    Industry compliance standards

    • Swiss Ordinance on Materials and Articles (SR 817.023.21)—Annex 10, printing inks
    • EU No 2020/1245, specific migration limits (SML) for food contact coatings
    • US FDA 21 CFR 175.300 (resinous and polymeric coatings)
    • Japan Food Sanitation Act for food printing inks

    Typical usage ratio

    • 3–12% by weight of the wet ink or coating blend,
    • Depends on resin system, flexibility needed, and end-use regulatory testing results.

    Downstream process integration

    • Added to resin-solvent mixture in batch or continuous ink blending,
    • Subjected to filtration, viscosity adjustment, and inline QC before filling press reservoirs.

    Final product types

    • Food contact gravure and flexo inks
    • Overprint varnishes for food wraps
    • Shrink sleeve and self-adhesive label coatings
    • Inner-lid and tamper-band print systems
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    Certification & Compliance
    More Introduction

    Triethyl Acetyl Citrate: Experience from the Production Line

    Real-World Insight into a Versatile Plasticizer

    Around our plant, Triethyl Acetyl Citrate (TEAC) has become a daily name among our colleagues. This product carries the model TEAC-99, reflecting purity at or above 99%, and stands out for its clarity, its gentle scent, and its balanced performance across a range of industries. After years of batch production and quality control, our technical staff have gathered insight into how TEAC behaves differently from other plasticizers and the real advantages it brings to formulators.

    Understanding Triethyl Acetyl Citrate

    The chemists in our team work day in and day out with citric acid esterification, fine-tuning reaction time and temperature to achieve products meeting tight monograph requirements, especially for TEAC-99. We base our process on reliable access to citric acid, acetic anhydride, and carefully sourced ethanol, minimizing byproducts and avoiding any detectable phthalates. This level of process control fosters a product that is not only high in purity, but also low in residual moisture and color, two properties our pharmaceutical customers pay close attention to.

    What’s inside each drum of TEAC comes from more than a simple reaction. Trained operators track each step, using gas chromatography and moisture analyzers to certify consistency from lot to lot. The final liquid should pour as a clear, almost colorless material, free from strong odors, and measure almost no measurable water—each batch is checked for color against APHA standards and for residual solvents below the international thresholds. This hands-on quality management builds a level of trust our partners depend on, particularly for pharmaceutical and food contact applications.

    Product Specifications and Why They Matter

    Over the years, the preferred grade—TEAC-99—has stabilized around the following characteristics: purity above 99%, low acid value (typically under 0.15 mg KOH/g), ester content above 97%, and refractive index within the narrow window of 1.437–1.442 at 20°C. Water content rarely goes above 0.2%. What looks like a list of numbers actually translates into product security. High purity supports the flavor, fragrance, and drug coating industries where impurities could disrupt appearance, taste, or shelf life. Color is monitored batch by batch to prevent the yellowing or haziness that could compromise a user’s process.

    Stability in standard storage conditions allows our clients to transport and stock larger volumes of TEAC-99, without facing rapid degradation or hydrolysis. Higher water content drastically shortens shelf life and encourages the growth of unwanted byproducts, so every drum leaving the plant is checked to avoid such failures down the supply chain.

    Direct Use Cases in Everyday Manufacturing

    Our biggest markets for Triethyl Acetyl Citrate include film coating in pharmaceuticals and food packaging, plasticization of medical devices, and the creation of nail polish as well as flavor carriers. Every week, our process specialists field calls from technical managers working on tablet coating lines who demand a plasticizer delivering the right combination of flexibility and rapid drying, which means minimal risk of sticking. With TEAC-99, several generics manufacturers confirm smoother application, predictable film integrity, and regulatory acceptability.

    For food packaging, end-users share the same priorities. Regulatory authorities generally recognize triethyl acetyl citrate as safe for direct food contact, and its clean profile—low migration, barely detectable odor, and absence of phthalates—matches current safety trends among multinational packagers. Our quality team regularly supports audits by sharing analytical results and stability studies specific to TEAC in food-contact scenarios. The result is a product reliable for use in wrapping films, gaskets, and soft bottle liners.

    One often overlooked but critical area is the care taken in handling the material. TEAC flows readily at room temperature, with viscosity that allows easy pumping or mixing, even in unheated tanks. Its mild, non-persistent odor helps maintain a comfortable work environment, an asset when switching over from harsher plasticizers like dibutyl phthalate (DBP) or diethyl phthalate (DEP). Workers dealing with sensitive manufacturing lines have less residue buildup to clean, thanks to TEAC’s minimal tendency to cling to surfaces.

    Where Triethyl Acetyl Citrate Sets Itself Apart

    Years ago, the preferred plasticizers were often phthalate-based, mostly due to sheer cost and strong plasticizing action. We have lived through the turning of the tide as regulatory actions and consumer expectations have reshaped the plasticizer landscape. Substituting TEAC-99 for phthalates in products like medical devices, pill coatings, and food packaging means clients avoid debates around endocrine disrupters, carcinogenic risk, or cumulative toxicity. Our R&D group doesn’t just look at technical specs; they look at years-long performance, global regulations, and market access.

    TEAC’s unique edge over some other citric acid esters, like triethyl citrate or tributyl citrate, comes from added acetylation of the central citric acid backbone. This small structural difference lowers volatility, softens odor even further, and reduces migration out of finished products. When scaled up in nail lacquer plants, for instance, formulators confirm fewer cases of tacky or slow-curing films. Coatings set quicker, with less need to adjust curing ovens or aging times.

    From a technical perspective, the extra acetyl group in TEAC-99 changes its behavior in water and oil environments. It dissolves quickly in ethanol, acetone, and most polymers used in pharmaceutical film coats or nail polishes. It has just enough water solubility to blend smoothly with aqueous dispersions while resisting water extraction once the film sets. Companies serious about reducing unwanted leaching from medical tubing and device coatings choose TEAC because of this chemical profile.

    Comparison with Triethyl Citrate and Other Alternatives

    Triethyl Citrate (TEC) and Triethyl Acetyl Citrate share much of the same starting chemistry, but our lab work repeatedly shows TEAC is less prone to migrate or leach after processing. TEC, being less hydrophobic, migrates faster under high moisture or elevated temperatures, a real concern for manufacturers shipping medical parts to humid climates. TEAC’s slightly higher molecular weight and the blocking from that acetyl group make it better for products that undergo high-temperature sterilization or long-term storage.

    Compared with tributyl citrate (TBC), another common alternative, TEAC-99 sits in an eco-friendlier spot for both regulatory review and end-user preference. Tributyl citrate plasticizes just as well, but lingering odor and skin contact toxicity show up more often in customer complaints. TEAC matches plasticization power while dropping extra side effects.

    Manufacturing Challenges and Solutions

    From the factory floor, maintaining consistent quality with TEAC-99 has required fine-tuning on several operational fronts. Reactor fouling and color drift stand out as the main issues. Small impurities in ethanol, improper water stripping, or out-of-spec acetic anhydride each add color or acidity to the final product. The team invests in double filtration, ultrasonic cleaning of reactors, and frequent replacement of gaskets and seals.

    Our plant also faces constant pressure from downstream users to avoid residual solvents like toluene or dichloromethane. Years back, we overhauled our process to use only ethanol as the reaction solvent, then vacuum distill off all volatiles. Every production campaign includes tests for volatile residue and a review of batch chromatography fingerprints. Technicians pull mid-reaction samples hourly, with line supervisors charting acid value and ester content in real-time. With this hands-on attention, production catches drift in reaction conditions before it results in an off-spec lot.

    Handling the scale-up from lab to full reactor often brings new wrinkles to light. For TEAC, reaction time and the speed of acetylation both matter—undercooked batches allow free citric acid to linger, raising acidity and damaging process yields. Staff on the night shift monitor pH, heat balance, and vacuum strength to make sure each run completes on time, every time.

    Supporting Formulators and End Users

    We spend as much time answering customer questions as we do mixing raw materials. Queries range from compatibility with different polymers, shelf-life under various climates, and stability during gamma sterilization, to the selection of food-safe antioxidants or storage tank materials. Our experience confirms that storing TEAC-99 in steel tanks with dry nitrogen headspace almost completely avoids both water uptake and contamination. Small practical tweaks—insulating transfer lines, using compatible pump seals, and monitoring drum temperature—let our customers avoid common pitfalls and maintain product at spec.

    TIAs sometimes worry about product shortages during audits or new launches, especially when demand spikes. Maintaining multiple parallel reactors and holding safety stocks gives us the flexibility to ramp up output during seasonal swings. This approach saves our regular clients from wrestling with long lead times or needing to switch to less-familiar plasticizers under deadline pressure.

    Quality Assurance from Raw Material to Shipping

    Drums of TEAC-99 headed for Europe look the same as those heading across Asia or North America. What often goes unseen is the routine stress testing on every lot; samples get exposed to sunlight, freeze-thaw cycles, and extended storage above 30°C before a single barrel leaves our plant. Liquid chromatography confirms the chemical makeup stays stable, with no significant breakdown over six months or more. We add unique lot codes on every shipment and keep ten-year retention samples for on-demand reanalysis if regulatory auditors come knocking.

    Our experience shows that labeling must be precise: each drum lists purity, acid value, water, color, and manufacturing date, with internal cross-checks so tracking an issue never turns into guesswork. Many of our clients work under cGMP environments, where ingredient traceability is not negotiable. Each batch includes a certificate of analysis and supporting chromatograms. Our plant supports customer by opening our labs to their inspectors, sharing analytical curves and supporting fast root-cause investigations if new questions arise.

    Regulatory Compliance and Practical Responsibility

    The road to regulatory acceptance means more than meeting the minimum. Our product development relies on close tracking of global shifts—no batch heads out without checking current standards from agencies like the FDA, EFSA, or Chinese Food Safety Law. Differences across jurisdictions can trip up even the best product; what passes muster as a polymer additive in one country might not in another.

    On-site compliance specialists keep logs for every compliance request, including BSE/TSE declarations, GMO statements, allergen status, and absence of heavy metals or intentionally added microplastics. Our documentation and open records help clients keep their own internal audits smooth and guarantee speedy responses during import checks or recall investigations.

    Sustainability is growing in importance and our R&D group remains focused on new methods for lower-waste production, from solvent recovery to renewable sourcing of base citric acid. Every ton shipped this year contains a higher recycling rate and tighter waste controls than even two or three years ago. Local environmental permitting increasingly depends on proof of clean, non-toxic effluent and minimal hazardous byproduct generation—so operational improvements have become an everyday effort.

    The Face of Change: Adapting to the Future of Plasticizers

    Demands on our TEAC-99 product keep growing not just because of legislation but because end-customers, whether in healthcare, cosmetics, or food, have upped their standards. Years of feeding into global R&D projects have taught us that no universal plasticizer exists—each formula, from enteric coating to PVC toys, sets its own balance between cost, safety, and technical effectiveness.

    Feedback from the field keeps us sharp. Formulators tell us where even a subtle odor matters, when viscosity matches are needed for efficient mixing, and when issues of interaction with pigments or resins can make or break a launch. As trends push for bio-based and biodegradable additives, our process team continues exploring new citrates, blending options, and structure modifications to stay a step ahead of the next regulatory, technical, or market-driven shift.

    Conclusion: Lessons Learned in Making Triethyl Acetyl Citrate

    Behind every kilogram of TEAC-99 stands a team fine-tuning each detail. No shortcut exists for delivering a product that meets global standards for safety, traceability, and stable performance. Years in production lines, feedback loops with users, and adaptation to an evolving regulatory scene confirm that a reliable product grows out of open conversation and continuous technical investment, more than from any quick fix or commodity trading.

    As the chemical world leans away from old plasticizers and toward greener, safer, and more performant alternatives, Triethyl Acetyl Citrate has made its mark. Experience from manufacturing runs, troubleshooting, and direct application feedback continues to shape our process and product, making TEAC-99 a trusted tool in the toolbox of manufacturers worldwide.