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HS Code |
764444 |
| Chemical Name | Polyethylene Glycol 4000 |
| Cas Number | 25322-68-3 |
| Molecular Formula | (C2H4O)n |
| Average Molecular Weight | 3800-4200 g/mol |
| Appearance | White to off-white powder or flakes |
| Odor | Odorless |
| Solubility In Water | Freely soluble |
| Melting Point | 53-58°C |
| Ph Of 10 Solution | 4.5-7.5 |
| Boiling Point | Decomposes before boiling |
| Density | 1.15 g/cm³ |
| Hygroscopicity | Hygroscopic |
| Storage Conditions | Store in a cool, dry place |
| Stability | Stable under recommended conditions |
| 用途 | Pharmaceuticals, cosmetics, food additives |
As an accredited Polyethylene Glycol 4000 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Polyethylene Glycol 4000 is packaged in a sealed, white HDPE drum containing 25 kg, with clear labeling and safety instructions. |
| Shipping | Polyethylene Glycol 4000 is typically shipped in tightly sealed, moisture-resistant containers such as fiber drums or polyethylene bags. It should be stored and transported in a cool, dry place, away from direct sunlight and incompatible substances. Ensure containers are clearly labeled and protected from physical damage during shipping. |
| Storage | Polyethylene Glycol 4000 should be stored in a tightly closed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, well-ventilated area, preferably at room temperature. Keep away from incompatible substances and strong oxidizing agents. Ensure containers are clearly labeled to prevent contamination. Follow all relevant safety regulations and guidelines for storage of chemical substances. |
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Purity 99%: Polyethylene Glycol 4000 with purity 99% is used in pharmaceutical tablet formulations, where it enhances solubility and bioavailability of active ingredients. Molecular Weight 4000 g/mol: Polyethylene Glycol 4000 of molecular weight 4000 g/mol is used in cosmetic creams, where it improves emollience and spreadability. Melting Point 53–58°C: Polyethylene Glycol 4000 with a melting point of 53–58°C is used in suppository bases, where it ensures controlled melting and uniform drug release. Viscosity 150-200 cP: Polyethylene Glycol 4000 with viscosity 150-200 cP is used in industrial lubricants, where it provides stable and consistent film formation. Low Ash Content <0.1%: Polyethylene Glycol 4000 with low ash content <0.1% is used in food processing aids, where it maintains purity and prevents product contamination. Moisture Content <1%: Polyethylene Glycol 4000 with moisture content less than 1% is used in powder formulations, where it prevents clumping and improves flowability. Stability Temperature up to 100°C: Polyethylene Glycol 4000 with stability temperature up to 100°C is used in chemical synthesis processes, where it withstands heat without degradation. Particle Size <200 µm: Polyethylene Glycol 4000 with particle size <200 µm is used in oral dosage forms, where it ensures uniform mixing and quick dissolution. Hydrophilic Grade: Polyethylene Glycol 4000 of hydrophilic grade is used in ophthalmic solutions, where it enhances water retention and provides effective lubrication. Non-Ionic Character: Polyethylene Glycol 4000 with non-ionic character is used in biochemical assays, where it minimizes protein denaturation and ensures assay accuracy. |
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Within our facility, Polyethylene Glycol 4000, often simply called PEG 4000, represents a cornerstone product in our polyether production line. Its reputation comes from years of consistent performance across pharmaceutical, food, cosmetic, and industrial applications. Thanks to our continuous investment in raw material control and batch consistency, the output from each reactor highlights the degree of reliability that formulation chemists expect from this excipient.
PEG 4000 is a medium molecular weight, solid-grade polymer produced by ethoxylation and polymerization of ethylene oxide, reaching a molecular weight close to 4000 Daltons. During synthesis, we've learned that careful attention to molecular distribution and residual impurities dictates downstream application performance, so we place real emphasis on purification and quality control at this stage. A white, waxy or powdery material, it comes in flakes or granular form, and dissolves quickly in water to produce clear, viscous solutions. Its melting range and other physical properties reflect our process discipline in achieving tight product specifications every batch.
There is a noticeable distinction between PEG 4000 and its siblings in the PEG range, such as PEG 200, PEG 400, PEG 6000, or PEG 8000. Every day, we see firsthand how changing molecular weight affects physical performance and end-user experience. PEG 4000, for instance, sits between liquid, low molecular weight grades (like PEG 200 or PEG 400) and higher, more rigid grades (such as PEG 6000 and PEG 8000). This middle ground makes PEG 4000 a popular choice for applications that require balanced solubility, viscosity, and melting behavior.
While lower molecular weight PEGs are fluids at room temperature and suit liquid preparations or lubrication, PEG 4000 provides a solid consistency that’s just right for molding and granulation. Its handling characteristics make it well suited for tableting in pharmaceuticals and for forming consistent suppository bases. We’ve seen customers switch between PEG 4000 and PEG 6000 to alter the hardness or disintegration speed of oral dosage forms or to influence the release rate of active ingredients; the decision often comes down to a tradeoff between melting point, processing temperature, and the desired physical robustness of the finished product.
Our technical team gets regular questions about replacing higher or lower PEGs in a process. PEG 4000’s melting range, around 50 - 60°C, provides a workable midpoint. This range allows us to design formulations that are stable at moderate temperatures but are still easy to process. If the molecular weight climbs too high, as with PEG 8000, the melting and handling require higher energy input that not all manufacturing setups can support. When the weight dips, like in PEG 1500, the softer consistency and greater hygroscopicity can cause flowability or stability problems in some dosage forms or confections.
At our site, we see PEG 4000 heading for pharmaceutical manufacturers more than anywhere else. It serves as a proven base material in solid oral tablets and capsules. PEG 4000 provides both binding power and plasticity, helping ensure robust compacts that resist chipping but still break down efficiently when swallowed. Lab work and plant trials confirm this with each validation batch: harder tablets and more uniform dissolution profiles reflect consistent excipient quality.
In suppositories, PEG 4000 blends well with higher and lower PEGs to adjust melting speed. Process engineers value the trouble-free fusion and mold release, proven by low product rejection rates. Over the years, we’ve worked side-by-side with development chemists who are chasing faster on-demand dissolution or slower, sustained release. PEG 4000 has become their primary tool to dial in these properties without unwanted side reactions or processing headaches.
Food companies use PEG 4000, too, mostly for its function as a carrier, stabilizer, or humectant. Bakers and confectioners use it in flavor delivery systems, icing, and coatings, where the balance between solubility and resistance to moisture loss is valuable. Our experience shows that food-grade PEG 4000’s taste neutrality lets it go unnoticed by the consumer, meeting both food safety requirements and regulatory standards we adhere to for each batch.
Cosmetic manufacturers also employ PEG 4000 to adjust viscosity in creams, pastes, or ointments and to promote moisture retention. Our quality team routinely tests its compatibility with common actives, fragrances, and pigments, making sure stability and texture stay uniform over shelf life. In toothpaste, its solid nature enables easy extrusion and glossy texture. In skin creams, the melting profile of PEG 4000 provides skin feel benefits without stickiness, supporting the claims our customers rely on in their product launches.
Industrial customers leverage PEG 4000 for binding and lubrication, especially in ceramics and rubber compounding. Its water solubility ensures clean burnout in ceramics, and we’ve received feedback from producers highlighting reductions in processing residue after switching to our grades of PEG 4000. The topic of ecological safety often comes up—PEG 4000 is non-toxic and leaves minimal residue, giving manufacturers a route toward cleaner processes and easier environmental compliance.
Producing PEG 4000 with consistent molecular weight, low impurities, and reliable physical properties demands strict process control at each production stage. Our experience has shown the importance of managing reaction conditions, solvent recovery, and the purification loop. The purification steps we use, such as vacuum stripping and multiple-stage filtration, go beyond basic removal of reagents and unreacted monomers. They are critical for minimizing color and odor while ensuring the absence of catalysts or trace metals.
Our control labs analyze every batch by measuring molecular weight distribution, moisture content, heavy metals, and bacterial levels. We have invested in modern gel permeation chromatography and real-time moisture analyzers, which provide direct insight into product quality, not just during final release but throughout intermediate steps. We’ve learned that catching off-spec results early keeps our production yield high and our customer complaints almost nonexistent.
Customers in regulated sectors expect transparency about residual solvents and trace impurities. In pharmaceuticals and food processing, low levels of ethylene oxide, dioxane, and heavy metals matter, so we routinely publish our analytical results. Our audits and client qualification visits focus on these measurable outcomes rather than marketing slogans. This open approach, rooted in regular laboratory validation and process review, supports both our supplier relationships and our reputation in the market.
Through customer feedback and day-to-day troubleshooting, we’ve discovered that users often worry about batch-to-batch consistency, especially in direct compression tableting or in high-speed food lines. Slight changes in melting behavior, color, or flow properties can disrupt production. For us, this means never leaving analytical checks for the end of the line—real process control happens throughout the reaction, purification, and blending stages.
Some processors express concern about long-term storage and handling. PEG 4000, due to its solid nature, isn’t as moisture-prone as lower PEGs. Nonetheless, we recommend protected storage because over time, high humidity or temperature cycling can lead to caking or surface crusting. In response, we package our material in double-layer polyethylene bags within fiber drums or waterproof sacks, then check packaging integrity before every shipment. We also maintain inventory turnover and environmental controls on our own premises, which keeps the material flowing freely and within spec even months after production.
Another question that comes up: “Can PEG 4000 be used as a direct replacement for PEG 6000 or 8000?” Our own trials show that simple substitution isn’t always a one-to-one proposition. The shift in molecular weight changes viscosity, melting behavior, and even the interaction with actives or flavors. Slowly incorporating PEG 4000 into development work, not just in the lab but on scaled production lines, helps avoid surprises. We support customer trials with free technical data, side-by-side batch reports, and on-site support when needed.
Demand for PEG 4000 has risen steadily over recent years, driven by expansion in both regulated (pharma and food) and specialty (cosmetic, industrial) sectors. Clean label expectations and regulatory pressure highlight the importance of material origin and traceability, a topic we’ve had to address with every new customer and audit. Because we control ethylene oxide sources, use closed-system reactors, and document every manufacturing step, we offer not just a chemical but an audited trail to every client. This documentation includes full chain-of-custody, batch genealogy, and compliance with local and international requirements, from pharmacopoeia standards to food contact approvals.
Sustainability is another emerging theme. Our process team tracks energy consumption and solvent recovery on every campaign, working toward smaller environmental footprints per kilogram produced. The non-bioaccumulative nature of PEG 4000 and its lack of toxicity in aquatic environments pushes it to the front in terms of environmental safety profiles for nonactive excipients. We’re beginning to see a shift in customer questions—clients want not just analytical specs, but also life cycle data and Green Chemistry metrics. Responding to that challenge, we supply environmental statements and are piloting a project to derive a portion of our ethylene oxide feedstock from bio-based sources.
The move toward biologics and advanced formulations, especially in pharmaceuticals, points to a lasting role for PEG 4000. It serves as a stabilizer for proteins, peptides, and biopharmaceuticals, thanks to its water solubility, chemical neutrality, and absence of immunogenicity. Our applications team partners directly with research groups developing PEGylated APIs, testing new process routes and particle sizes for better stability and reduced aggregation risk.
Large-scale users order PEG 4000 in drum or tote quantities, while smaller R&D teams favor pail or bag sizes to suit both bench work and pilot-scale trials. Over the years, we’ve seen the needs of high-throughput plants diverge from specialty producers. To support each segment, our warehouse team offers tailored packaging: anti-static liners for electronics-grade material, moisture-barrier bags for export, and color-coded drums for easy identification of food, pharma, or industrial grades. Each packaging batch includes a unique lot identifier to backtrack performance data if troubleshooting becomes necessary.
Quality continues beyond the lab. We maintain open communication from order to delivery, enabling customers to know exactly which production date, lot, and operating conditions produced their PEG 4000. Any deviation—whether a shipment delay, specification tightening, or customer-requested certificate—triggers an internal review involving multiple teams. While this may slow routine batch release, it is how we avoid recalls and build long-term trust. Such discipline is hard-earned and, after decades in production, pays off in robust customer partnerships.
Every year, new application ideas arrive at our technical desk—a surfactant modifier for green detergents, a humectant in non food-contact biodegradable plastics, a carrier for soil moisture retention agents, or an emollient for veterinary ointments. We evaluate feasibility not just in the lab, but in our full-scale process: Will it process efficiently? Can it be packed and transported safely? Does it meet regulatory limits in all intended markets? Though specific modifications (like particle size, melting point fine-tuning, or color) may mean extra steps, our batch flexibility and technical experience usually allow us to respond within a single plant campaign.
Traceability starts long before the polymerization kettle runs. Every feedstock lot, catalyst addition, and process variable sits logged in our MES, accessible for customer review on request. Periodic process audits—sometimes with client teams on-site—verify both our internal compliance and our transparency. Batch release is based on both in-house results and retained samples shipped for third-party analysis, if required by clients’ own QA programs.
Over the years, third-party audits have strengthened the culture of open records and traceable manufacturing. Our facility’s central lab holds reference samples and batch paperwork going back a decade, a level of documentation uncommon in less regulated sectors. Trends in impurities or specification drift trigger root-cause reviews, often before a complaint ever emerges. This preventive framework pays off by making sure every shipment of PEG 4000 matches not just written specifications, but the tacit expectations built up over many business cycles with customers.
Client queries extend into the realm of regulatory documentation. To address this, we provide pharmacopoeia certificates, food contact statements, and REACH or TSCA compliance updates as standard for each batch intended for pharmaceutical or food use. As part of ongoing commitment, our regulatory group maintains up-to-date knowledge of country-specific limits on ethylene oxide, 1,4-dioxane, and other trace constituents. These limits change from region to region, and keeping up means collaborating directly with regulators, not just reacting to recalls or market withdrawals.
Technical requests for performance data have grown as end users aim to differentiate their own products. While we supply traditional test results—appearance, melting point, viscosity, heavy metals—we also generate custom application studies. Whether it’s a tablet compaction trial, a flavor solubility test, or a prototype cream stability run, our support comes with both real-world experience in scale-up and the data needed to back new product launches.
To keep PEG 4000 aligned with evolving industry expectations, we participate in customer-driven innovation programs. These involve side-by-side trials, feedback sessions, and rapid revision of internal standards. Changes in end-user requirements—for instance, new color targets, tighter residue limits, or organic-compliant certifications—lead us to adapt raw material screening, plant operations, and downstream packaging. This flexibility springs from the organizational experience built up over years handling feedback, audits, and the pressure of critical supplier status.
Market shifts often start as minor trends but soon become broad drivers. The growing push for sustainable chemistry, and the scrutiny of possible impurities like 1,4-dioxane, have led us to review every synthesis and purification stage. Based on extensive plant histories, our engineering team retrofits equipment or tunes process flows whenever real-world data show room for improvement. New reactors, improved monitoring, and solvent minimization all feed into a better end product, fewer disruptions, and cleaner compliance audits.
The evolution of digital documentation also means clients now want batch data available in formats ready for GMP, ERP, or digital twin systems. Our IT and technical support teams regularly field integration requests, sometimes processing digital certificates and tailored batch dossiers for pharma or food companies. As these requirements influence how we report and trace each PEG 4000 shipment, our responsiveness becomes as important as chemical performance.
Across decades of production and customer support, our experience with PEG 4000 shows the value of detailed process understanding, customer interaction, and ongoing improvement. We see real user pain points and design both our process and communication around those needs. By ensuring each batch carries the hallmarks of reliability, safety, and traceability, we reinforce trust in a product that sits at the foundation of many complex modern applications.
As formulation and regulatory requirements evolve—whether for a pediatric medicine, specialty food, premium cosmetic, or industrial blend—we keep adapting. From the shop floor to the technical desk, we remain committed to transparency, responsive development, and world-class quality standards for every kilogram of PEG 4000 that leaves our facility.