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HS Code |
648325 |
| Chemical Name | Polyethylene Glycol 6000 |
| Abbreviation | PEG 6000 |
| Molecular Formula | (C2H4O)n |
| Average Molecular Weight | 6000 g/mol |
| Physical State | Solid |
| Appearance | White to off-white flakes or powder |
| Odor | Odorless |
| Solubility In Water | Freely soluble |
| Melting Point | 56-63 °C |
| Ph In Solution | 4.5 – 7.5 (5% w/v solution) |
| Density | 1.12–1.15 g/cm3 |
| Cas Number | 25322-68-3 |
As an accredited Polyethylene Glycol 6000 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Polyethylene Glycol 6000 is packaged in a 500g sealed, white, high-density polyethylene bottle with a tamper-evident cap and label. |
| Shipping | Polyethylene Glycol 6000 (PEG 6000) is shipped in tightly sealed, moisture-resistant containers, such as fiber drums, plastic drums, or multi-layered bags, each typically weighing 20-25 kg. The product should be stored and transported in cool, dry conditions, away from direct sunlight, heat sources, and incompatible materials to maintain quality and stability. |
| Storage | Polyethylene Glycol 6000 should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Keep away from incompatible substances, such as strong oxidizing agents. Store at room temperature and ensure good laboratory practices to avoid contamination and degradation of the chemical. |
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Molecular Weight: Polyethylene Glycol 6000 with a molecular weight of 6000 g/mol is used in pharmaceutical tablet formulations, where it enhances controlled drug release profiles. Purity: Polyethylene Glycol 6000 with 99% purity is used in cosmetics manufacturing, where it ensures product safety and consistent emollient performance. Melting Point: Polyethylene Glycol 6000 with a melting point of 58°C is used in ointment bases, where it provides optimal spreadability and texture. Particle Size: Polyethylene Glycol 6000 with a particle size of less than 100 microns is used in powdered drink mixes, where it aids in uniform dispersion and solubility. Viscosity Grade: Polyethylene Glycol 6000 with high viscosity grade is used in adhesives, where it improves bonding strength and application stability. Stability Temperature: Polyethylene Glycol 6000 with stability up to 100°C is used in industrial lubricants, where it maintains functional viscosity under operational heat. Moisture Content: Polyethylene Glycol 6000 with moisture content below 0.5% is used in food coatings, where it prevents clumping and preserves product integrity. Compatibility: Polyethylene Glycol 6000 with broad chemical compatibility is used in personal care formulations, where it facilitates homogeneous ingredient blending. Residue: Polyethylene Glycol 6000 with low residue content is used in medical device coatings, where it minimizes extractables and leachables for patient safety. Hydrophilicity: Polyethylene Glycol 6000 with high hydrophilicity is used in water-soluble film applications, where it accelerates dissolution rates. |
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You find a lot of opinions out there about raw materials, but as a producer, we see Polyethylene Glycol 6000 at all phases – from the first reaction to the drum, then right through quality checks and out the door to the industries that depend on it. There’s a plain truth in chemistry: if your process doesn’t run clean, your end user feels it. PEG 6000 isn’t just a base chemical you throw into a mix. It’s a backbone in a surprising number of processes, and getting its specifications right each time is what keeps productions stable everywhere from pharma lines to food plants.
Unlike lighter grades, PEG 6000 doesn’t behave unpredictably under slight shifts in humidity or temperature. In our daily work, the solid, flake, or powder forms of PEG 6000 allow for a controlled, measured addition. Granules flow smoothly without the sticky mess of lower-weight glycols that cling to conveyors and introduce dosing errors. For us, quality control isn’t some distant concept—it’s a matter of avoiding downtime, batch rejections, and costly waste.
The molecular weight of 6000 sits at a sweet spot. It creates viscosity where you need it, but it doesn’t bog down blending or cleaning. Mixing a batch by hand gives you an immediate sense of how well a product integrates, and with PEG 6000, clumping doesn’t happen the way it might with heavier grades. You avoid inconvenient agglomerates that so often slow down a continuous process line. That’s not theory; we see it daily on our own floors and in our own test batches.
We measure quality in the smallest details––moisture content, molecular distribution, clarity. In polyethylene glycol production, these can drift if you relax your process. One regular check we keep on is for peroxide content. Left unchecked, this can introduce variability that ripples through a customer’s process. Our approach is rooted in repeatable, verifiable analysis. Every batch passes through established labs, with samples tagged and tracked right down to the operator who handled it.
Specifications run more precise here than across-the-board industry averages. Pharmaceutical inputs demand that you not only meet published standards, but hold a line against bioburden, heavy metals, and other contaminants. Polyethylene glycol flows downstream into products that get applied to skin, ingested in tablet coatings, or blended into food additives. We live by the old factory saying: measure more, discard less.
A material’s popularity doesn't happen by committee—it’s cemented by the work it does in the field. PEG 6000 landed in widespread use because formulators, coating-line managers, and even contract packagers saw that it solved daily headaches. For instance, the hydraulic press operator at a tablet manufacturer cares about how the binder blends and releases from the mold, not just the published viscosity at 20°C. Repeated, reliable behavior means fewer process interruptions—and that’s the practical advantage PEG 6000 delivers.
In cosmetics, viscosity is just the start. PEG 6000 holds emulsions steady and delivers a thicker, more desirable texture. You can blend with oils, waxes, and pigments without risking separation on the shelf. That’s something we’ve learned by visiting customer sites and watching compounding in real time, not just reading papers.
There’s more to making PEG 6000 than electrical input and distillation columns. Raw ethylene oxide and water react in controlled conditions, but keeping the reaction consistent takes constant monitoring. Capping, purification, and drying separate a product that passes strict scrutiny from a batch that risks introducing impurities downstream. We calibrate every vessel and exercise strict batch separation to avoid cross-contamination.
Shipping and packaging decisions are just as critical as reaction conditions. We use lined, clean containers to protect against moisture and particulate contamination. It matters in practice: stricter packaging leads to fewer failures due to caking, and that prevents hassle during customer intake and storage. By incorporating sealing technologies that work in both humid coastal regions and dry climates, we support the widest possible range of storage constraints faced by users.
Misinformation lingers around polyethylene glycols, particularly regarding cross-contamination with diethylene glycol or dioxane residues. We invest in analytical equipment and professional training for our staff because the risk comes with a human cost, not just regulatory fines. Deviation from standard process controls or shortcuts leads to out-of-spec product. We track all feedstock sources and document every step, because trust is built batch by batch, not just by proclamation.
Some buyers approach us expecting magic bullet solutions—PEG 6000 doesn’t make up for poor formulation design. It works best when you adjust solubility, moisture, and active ingredient ratios upfront. We’ve spent long nights with R&D teams troubleshooting failed blends: changing PEG grade, heating profile, or sequence of addition can mean the difference between success and unmanageable product separation. Hands-on experience always beats guesswork or faith in untested supplier promises.
With lower molecular weight PEGs like 400 or 2000, volatility and hygroscopicity increase. They pull water from the air and can throw off sensitive formulas, particularly in pharmaceuticals and foods. PEG 6000, with its higher molecular weight, brings more stability and less flavor taint or migration in food contact settings. That’s why direct-contact food additives, sensitive creams, and molded personal care goods rely on our grade for taste neutrality and all-around safety.
Moving up to PEG 20,000 or higher, flowability turns into a problem and full dissolution rates drop. We’ve fielded technical calls from customers frustrated by undissolved specks in solution—issues easily avoided by sticking with PEG 6000, which disperses more evenly and fully in standard process equipment. UV transparency, melting range, and bulk density all line up for trouble-free production, especially in multipurpose factories that handle short runs or custom projects.
Lab data enters production by way of working parameters set on the ground. Melting point (usually 56–63°C for PEG 6000) signals when to preheat blending kettles and when to cool to avoid scorching. Bulk density means something when you’re calculating loading limits for a pneumatic hopper. Viscosity at typical addition rates tells mixers whether they’ll see clumping. People might overlook these small numbers, but on a crowded factory floor, precision keeps schedules on track.
We verify absence of residual catalysts because even parts-per-million levels can cause yellowing in sensitive film coatings or degrade taste in softgels and confections. Our downstream customers run their own checks, and open-door audits follow our production line from raw inputs to finished containers. That transparency builds the kind of business relationship that lasts orders, not just one-off sales.
Here is where practicality trumps theory: compressible binders in direct-compression tablets, texture agents in medical gels, solubilizers in ODT (orally disintegrating tablets)—PEG 6000 is often the go-to solution. In veterinary applications, it helps deliver reliable dosing, blends without clumping, and conforms to animal feed safety standards that parallel those for humans. In personal lubricants, clarity, mildness, and consistent feel matter directly to the user.
In the agricultural sector, formulating soluble powder and wettable granule products relies on the flow and dispersibility qualities PEG 6000 brings. When you’re clamping a bag in a fertilizer line, the ease at which granules pour into a feeder weighs directly on productivity. Blockage and bridging grind process lines to a halt; PEG 6000 helps skirt those bottlenecks.
Every industry faces the pressure to reduce environmental impact. Water reuse and waste minimization aren’t just catchphrases - they’re key to our long-term ability to keep supplying PEG 6000. We continuously audit energy inputs, drive down residual monomers, and reduce off-spec waste through in-process sampling and real-time adjustments. Our by-product capture systems and solvent recovery efforts let us use fewer virgin inputs—another benefit that goes well beyond paperwork compliance.
Sourcing ethylene oxide with full traceability and ensuring proper storage are acts of responsibility—not just a matter of keeping licenses up to date. End-users want assurance that their ingredients travel through clean, monitored pipes and tanks. We invite customer quality teams to walk our lines, view our real-time monitoring dashboards, and take samples for independent analysis. It only takes one contaminated batch to lose confidence, and that reminder keeps us sharp every shift.
We get calls from developers and process engineers deep into scale-up, often after confronting unexpected results when switching between PEG grades or suppliers. Changing a PEG means thinking through solubility, set time, appearance, and even label compliance. Our technical experts don’t deal in hypotheticals—they have seen the pitfalls of over- or under-dosage, missequencing, and cross-reactions with active pharmaceutical ingredients.
To sidestep major setbacks, we take the approach of getting on the phone, reviewing batch sheets, and suggesting small but relevant process tweaks: sequence of addition, blending times, temperature ramps. Proven fixes save time, material, and frustration. Our commitment is to seeing partners succeed, not just ship and forget a pallet. That’s what sustainable manufacturing partnerships look like.
Raw material volatility affects both cost and confidence. We keep up by locking in supplier relationships and maintaining inventory that cushions against production hiccups. Over the past few years, as pharmaceutical and food output surged, we kept lead times reliable—not by guessing, but by overhauling inventory management and using demand forecasts driven by real sales, not optimism.
Changes in global health regulations, migration limits in food contact materials, and shifting customer specs have forced us to recalibrate analytical techniques. Every uptick in detection sensitivity means we revisit baseline tests, realign instrument calibration, and sometimes re-invest in up-to-date technology. Our expertise comes through in how fast we adapt and how rarely our PEG 6000 batches get flagged in incoming inspection.
Polyethylene Glycol 6000 serves a purpose that’s become clearer through thousands of batches produced—and with direct feedback from customers in pharmaceuticals, food, and industrial sectors. We have learned that even a small variance in process or storage affects more than just us; it ripples forward into the hands of formulators, plant managers, quality controllers, and end users. Commitment to consistent process, vigilant analysis, and straight communication is what lets us supply a product that meets more than written specs: it supports processes that keep shelves stocked and factories running.