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PEG 400
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| Names | |
|---|---|
| IUPAC name
Polyethylene glycol
| |
| Identifiers | |
| ChemSpider |
|
| UNII | |
| Properties | |
| C2nH4n+2On+1, n = 8.2 to 9.1 | |
| Molar mass | 380-420 g/mol |
| Density | 1.128 g/cm3 |
| Melting point | 4 to 8 °C (39 to 46 °F; 277 to 281 K) |
| Viscosity | 90.0 cSt at 25 °C, 7.3 cSt at 99 °C |
| Hazards | |
| Flash point | 238 °C (460 °F; 511 K) |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
|
30 mL/kg, orally in rats |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
PEG 400 (polyethylene glycol 400) is a low-molecular-weight grade of polyethylene glycol. It is a clear, colorless, viscous liquid. Due in part to its low toxicity, PEG 400 is widely used in a variety of pharmaceutical formulations.
Chemical properties
[edit]PEG 400 is strongly hydrophilic. The partition coefficient of PEG 400 between hexane and water is 0.000015 (log), indicating that when PEG 400 is mixed with water and hexane, there are only 15 parts of PEG400 in the hexane layer per 1 million parts of PEG 400 in the water layer.[1]
PEG 400 is soluble in water, acetone, alcohols, benzene, glycerin, glycols, and aromatic hydrocarbons. It is not miscible with aliphatic hydrocarbons nor diethyl ether. Therefore, reaction products can be extracted from the reaction media with those solvents.
References
[edit]- ^ T. Y. Ma; D. Hollander; P. Krugliak; K. Katz (1990). "PEG 400, a hydrophilic molecular probe for measuring intestinal permeability". Gastroenterology. 98 (1): 39–46. doi:10.1016/0016-5085(90)91288-h. PMID 2293598.
- The Merck Index, 11th Edition
- Handbook of Pharmaceutical Excipients
PEG 400
View on Grokipediafrom Grokipedia
Polyethylene glycol 400 (PEG 400) is a synthetic, low-molecular-weight polyether compound composed of repeating units of ethylene oxide, with an average molecular weight of approximately 400 daltons. It is produced through the anionic ring-opening polymerization of ethylene oxide using water or ethylene glycol as an initiator and an alkaline catalyst such as sodium hydroxide. This results in a clear, colorless, viscous liquid that is highly hydrophilic, miscible with water, and soluble in many organic solvents like ethanol and acetone, but insoluble in non-polar solvents such as hydrocarbons.[1][2]
In pharmaceuticals, PEG 400 functions primarily as an excipient, serving as a solvent, solubilizer, plasticizer, and lubricant in various dosage forms including oral capsules, topical ointments, and ophthalmic solutions. It enhances the bioavailability of poorly soluble drugs by improving their dissolution and is commonly incorporated into eye drops, such as those for dry eye relief, where it acts as a lacrimomimetic to lubricate the ocular surface and stabilize the tear film. Additionally, PEG 400 is utilized in cosmetics as a humectant, emollient, and carrier for active ingredients, helping to retain moisture in formulations like creams, lotions, and shampoos. In the food industry, it is approved as a direct additive for uses such as a binder, plasticizer, lubricant, and stabilizer in various applications including food tablets and nonnutritive sweeteners in accordance with FDA regulations for polyethylene glycols with mean molecular weights between 200 and 9,500.[3][4][5]
PEG 400 is characterized by low acute toxicity, with oral absorption typically less than 0.5% in humans, and it is considered biologically inert and safe for approved applications by regulatory bodies including the U.S. Food and Drug Administration (FDA). Its poor systemic absorption minimizes potential risks, though high oral doses may cause gastrointestinal effects like osmotic diarrhea. Overall, its biocompatibility and versatility have made it a staple in medical, cosmetic, and industrial products since its commercial development in the mid-20th century.[1][3][5]
Overview
Definition and Nomenclature
PEG 400 is a synthetic polyether compound derived from the polymerization of ethylene oxide, characterized by an average molecular weight ranging from 380 to 420 g/mol, which corresponds to an oligomer with approximately 8 to 9 repeating units in the general formula H(OCH₂CH₂)_nOH.[6][7] The term "PEG" is an abbreviation for polyethylene glycol, a family of hydrophilic polymers where the numeric suffix, such as "400," denotes the approximate average molecular weight in daltons, reflecting the degree of polymerization and polydispersity of the chain lengths.[6][3] This naming convention differentiates PEG 400 from higher-molecular-weight variants like PEG 3350, which features longer chains (n ≈ 75-76) and a solid, waxy physical state at room temperature, in contrast to the viscous liquid form of PEG 400 due to its shorter chain length.[8][9] Polyethylene glycols, including PEG 400, were first synthesized in laboratory settings in 1929 by Staudinger and Schweitzer through the anionic polymerization of ethylene oxide, with commercial-scale production emerging in the 1930s via base-catalyzed processes developed by companies such as Union Carbide.[10] PEG 400 gained prominence in industrial applications following World War II, leveraging its solubility and low toxicity for formulation purposes.[10]Physical Characteristics
PEG 400 appears as a clear, colorless to slightly yellow viscous liquid at room temperature.[11] It has a density of 1.12–1.14 g/cm³ at 20°C.[12] The material exhibits a viscosity of approximately 90 mPa·s at 25°C, contributing to its flow characteristics in liquid form. The melting point of PEG 400 ranges from 4–8°C, allowing it to remain liquid under typical ambient conditions.[11] Its boiling point exceeds 250°C, though the compound decomposes prior to reaching a true boiling state.[6] PEG 400 is hygroscopic, readily absorbing moisture from the atmosphere, which helps maintain its liquidity in contrast to higher molecular weight polyethylene glycols that solidify.[6] The substance is nearly odorless with a mild scent. It possesses a slightly sweet taste.[13]Chemical Properties
Molecular Structure
PEG 400, or polyethylene glycol with an average molecular weight of approximately 400 Da, is represented by the chemical formula H(OCH₂CH₂)_nOH, where n denotes the average degree of polymerization around 9.[12][14] This formula reflects its composition as a linear polymer consisting of repeating ethylene oxide units, –CH₂CH₂O–, capped at both ends by hydroxyl groups, forming a flexible chain that imparts hydrophilic character due to the polar ether linkages and terminal alcohols.[6] Unlike a discrete chemical compound, PEG 400 exists as a polydisperse mixture, encompassing a distribution of oligomeric chains with varying lengths centered around the 400 Da average, typically characterized by a polydispersity index (PDI) of 1.1 to 1.2.[14] This heterogeneity arises from the polymerization process and is routinely confirmed through techniques such as gel permeation chromatography (GPC), which separates chains by hydrodynamic volume to reveal the molecular weight distribution.[14] PEG 400 is derived from the polymerization of ethylene oxide monomer (C₂H₄O), but as the hydrated polymer, it incorporates water to form the extended polyether backbone, distinguishing it from the cyclic epoxide precursor.[15]Solubility and Stability
PEG 400 exhibits high solubility in a variety of polar solvents due to its hydrophilic polyether chain structure. It is infinitely miscible with water, allowing for the formation of clear aqueous solutions without phase separation or precipitation.[16] Additionally, PEG 400 is very soluble in ethanol, acetone, and chloroform, which facilitates its use in mixed solvent systems for pharmaceutical formulations.[17] In contrast, it shows limited solubility in non-polar solvents, being only partially soluble in aromatic hydrocarbons and practically insoluble in aliphatic hydrocarbons and mineral oils.[17] Thermally, PEG 400 demonstrates good stability up to temperatures of 150–200°C, with low volatility that prevents significant evaporation under standard processing conditions.[18] At higher temperatures exceeding 200°C, thermal decomposition occurs, primarily yielding ethylene glycol and formaldehyde as degradation products through chain scission and depolymerization mechanisms.[19] This decomposition is more pronounced in dry conditions, where oxidative processes can accelerate breakdown even at moderately elevated temperatures around 75°C.[20] Chemically, PEG 400 is resistant to hydrolysis under neutral and mildly acidic or basic conditions, maintaining integrity across a pH range of 4–10 without significant degradation.[21] It remains stable in the presence of dilute acids and bases, but exposure to strong oxidants, such as potassium periodate in alkaline media, can lead to oxidation of the terminal hydroxyl groups, forming long-chain aldehydes and minor amounts of carboxylic acids.[22] This oxidative vulnerability underscores the need for antioxidants in formulations prone to aerial exposure.[23] As a hygroscopic material, PEG 400 readily absorbs moisture from humid environments via hydrogen bonding with its terminal hydroxyl groups and ether oxygens, which helps preserve its liquid state and prevents crystallization even at high relative humidities.[24] This property contributes to its stability in aqueous or semi-aqueous systems, where it forms stable solutions without phase changes under typical storage conditions.[25]Production
Synthesis Process
PEG 400 is synthesized through the ring-opening polymerization of ethylene oxide using water or ethylene glycol as the initiator. In this process, ethylene oxide, a cyclic ether, undergoes nucleophilic attack by the hydroxide ion derived from water, leading to the formation of a linear polymer chain with hydroxyl end groups. The reaction is typically conducted in the presence of an acidic or basic catalyst to facilitate the polymerization, with basic catalysts such as sodium hydroxide being commonly employed for producing low molecular weight PEGs.[10] The fundamental reaction can be represented by the simplified equation: where averages around 9 for PEG 400, corresponding to a molecular weight of approximately 400 Da. This polymerization proceeds via anionic (oxy anionic) or cationic mechanisms, depending on the catalyst; the anionic pathway, initiated by alkoxides under basic conditions, yields well-defined chains with narrow polydispersity due to its living character, while cationic mechanisms under acidic conditions can introduce branching but are less common for linear PEG 400.[10] Control of the molecular weight in PEG 400 synthesis is primarily achieved by adjusting the monomer-to-initiator ratio, with an excess of water relative to ethylene oxide ensuring the low degree of polymerization required. Reaction conditions, such as short reaction times or low monomer concentrations, further contribute to limiting chain growth and obtaining the target low molecular weight, resulting in a Poisson distribution of chain lengths characteristic of living polymerizations.[10] Following polymerization, purification involves the removal of unreacted ethylene oxide, which is accomplished through vacuum distillation to ensure residual levels below regulatory limits. The catalyst is then neutralized, typically by quenching with an acid such as acetic acid for basic catalysts, followed by filtration or precipitation to isolate the product.[26]Commercial Production
PEG 400 is commercially produced through the anionic ring-opening polymerization of ethylene oxide, a key raw material derived from the catalytic oxidation of ethylene sourced from petroleum refining processes, with water or ethylene glycol serving as the initiator to control the degree of polymerization and achieve the desired average molecular weight of approximately 400 Da.[27] This process occurs on an industrial scale in specialized reactors designed to handle the reactive and volatile nature of ethylene oxide safely. The manufacturing typically employs either batch or continuous polymerization methods under elevated temperatures of 120–140°C and pressures to facilitate the exothermic addition reaction, ensuring efficient conversion while minimizing side reactions.[28] Major global producers include The Dow Chemical Company and BASF, which operate large-scale facilities to meet demand across pharmaceutical, cosmetic, and industrial sectors.[29] Global production of polyethylene glycols, including PEG 400, surpassed 450,000 metric tons in 2024, with PEG 400 comprising a notable portion due to its widespread use; the process is energy-intensive primarily owing to the requirements for high-pressure containment and thermal management of the polymerization.[30] Quality control in commercial production rigorously adheres to pharmacopeial standards to limit residual impurities from the synthesis, such as unreacted ethylene oxide (not more than 10 ppm per USP, 1 ppm per EP) and the byproduct 1,4-dioxane (not more than 10 ppm per both USP and EP), achieved through vacuum stripping and purification steps followed by analytical verification using gas chromatography.[31][32]Applications
Pharmaceutical Applications
PEG 400 functions as a key excipient in pharmaceutical formulations, primarily serving as a solvent and solubilizer for active pharmaceutical ingredients (APIs) with poor water solubility. Its high hydrophilicity and miscibility with water and organic solvents enable it to dissolve drugs effectively in various dosage forms, including oral liquids, injectables, and soft gelatin capsules, thereby enhancing drug stability and bioavailability. According to the FDA Inactive Ingredient Database, PEG 400 is approved for oral administration in forms such as capsules, elixirs, solutions, suspensions, and syrups, with maximum potencies ranging from 4.4 mg to 324.5 mg per unit dose and up to 1378 mg daily exposure.[33] For example, in ibuprofen syrup formulations, PEG 400 is combined with other cosolvents like propylene glycol at concentrations up to 40% w/v to achieve complete solubilization of the API, facilitating uniform drug delivery in pediatric and adult oral suspensions.[34] In parenteral applications, PEG 400 acts as a solubilizing agent in intramuscular and intravenous injections, where it is permitted at concentrations up to 18-20.3% v/v or 75.58% w/v, equivalent to a maximum of 7470 mg per dose.[35] This use supports the formulation of injectable solutions for APIs requiring enhanced solubility, such as in antibiotic or analgesic preparations, while maintaining low toxicity profiles suitable for systemic administration. Additionally, PEG 400 contributes indirectly to the efficacy of PEGylated therapeutics—where higher molecular weight PEGs are conjugated to proteins or drugs—by serving as an excipient that improves overall formulation stability and API dispersion without altering the conjugation chemistry itself.[6] As a vehicle in topical and ophthalmic products, PEG 400 provides viscosity modification and lubrication, forming the base for ointments, creams, and eye drops. In ophthalmic solutions, it is approved at up to 4% w/w, as seen in artificial tear formulations like Systane Ultra, where 0.4% PEG 400 combines with propylene glycol to relieve dry eye symptoms by augmenting tear film stability and reducing irritation.[36] For topical creams and gels, concentrations up to 7.5% are utilized to enhance API penetration and moisturization. PEG 400 is also included in laxative formulations at lower doses than higher molecular weight PEGs (e.g., PEG 3350), acting as a solvent to improve consistency and mild osmotic effects in oral suspensions or soft capsules.[37] Studies demonstrate that PEG 400 can boost oral bioavailability of certain BCS Class III drugs, such as ranitidine and cimetidine, by 34% or more through mechanisms involving increased gastrointestinal absorption and reduced efflux transporter activity.[38][39] Overall, PEG 400's approval in numerous FDA New Drug Applications underscores its safety and versatility as an inactive ingredient across dosage forms, with oral solutions commonly incorporating up to 30% to optimize API dissolution while adhering to regulatory limits.[33]Cosmetic and Personal Care Applications
PEG 400 serves as a versatile ingredient in cosmetic and personal care formulations, primarily functioning as a humectant to attract and retain moisture in the skin and hair, thereby preventing dryness in products such as creams, lotions, and shampoos.[40][41] In moisturizers, it is typically incorporated at concentrations of 5-10% to enhance hydration without compromising texture, leveraging its water-binding properties to maintain skin suppleness during application.[42] This hygroscopic quality, derived from its polymeric structure, allows PEG 400 to absorb atmospheric moisture, making it ideal for daily hygiene items like body washes and facial cleansers where sustained moisture is essential.[43] As an emulsifier and solubilizer, PEG 400 stabilizes oil-in-water mixtures in emulsions, ensuring uniform distribution of ingredients in formulations like soaps and toothpaste, while also dissolving lipophilic components such as fragrances and essential oils that would otherwise separate.[40][44] Concentrations in these products generally range from 1-20%, promoting better spreadability and a non-greasy feel upon application.[45] In hair conditioners, it aids detangling by coating strands and reducing friction, often at 1-5% to improve manageability without residue buildup.[46] In deodorants, PEG 400 acts as a carrier for active agents, facilitating even application and enhancing product efficacy in underarm hygiene products at levels around 1-3%.[40][42] Similarly, in lip care formulations like balms, it contributes to smoothness by solubilizing waxes and oils, typically at low concentrations to provide a lightweight, hydrating layer on the lips.[47] Overall, these roles enable PEG 400 to improve sensory attributes across beauty and hygiene items, from shampoos to skin emollients, at usage levels of 1-20% depending on the desired viscosity and stability.[43][45]Industrial Applications
PEG 400 serves as a versatile plasticizer and lubricant in various industrial manufacturing processes, enhancing flexibility and processability in materials such as inks, resins, and rubber compounds. In printing inks, it functions as a humectant, solvent, lubricant, and dye carrier, preventing drying and improving flow properties.[48][49] For rubber production, PEG 400 acts as a mold-release agent and lubricant for both natural and synthetic rubbers, facilitating easier demolding while being readily removable with water.[48][49] In resin formulations, particularly urea and polyester types, it improves plasticity and water dispersibility, aiding in the creation of flexible coatings.[50][49] In the food industry, PEG 400 (mean molecular weights 200-9,500) is approved for use as a direct food additive under 21 CFR 172.820 for purposes such as a binder, plasticizing agent, lubricant, and adjuvant, and as a component of defoaming agents in processing under 21 CFR 173.340, in amounts not exceeding those reasonably required for the intended technical effect.[5][51] Its low toxicity and solubility properties make it suitable for these roles without altering food quality.[52] Beyond these, PEG 400 finds application as a carrier and excipient in pesticide and agrochemical formulations, where its humectant nature helps reduce dusting and improve solubility of active ingredients.[49] It also serves as a humectant in tobacco processing to maintain moisture levels, and as a viscosity modifier in paints, acting as a binder, dispersant, and flow enhancer in water-based and latex formulations to optimize application consistency.[53][48][54] Overall, PEG 400's industrial consumption in non-pharmaceutical sectors, including lubricants and related applications, reaches thousands of tons annually, underscoring its scale in manufacturing.[55] Its moderate viscosity contributes to these roles by providing effective lubrication without excessive thickening.[48]Safety and Regulations
Toxicity Profile
PEG 400 exhibits low acute toxicity, with an oral LD50 greater than 30 g/kg in rats, indicating minimal risk from single high exposures.[56] It causes minimal skin and eye irritation and is non-sensitizing in standard dermal tests. In chronic exposure studies, PEG 400 shows no evidence of carcinogenicity or reproductive toxicity across standard animal models, including rats and rabbits.[57] At high oral doses exceeding 10 g/day, it may induce gastrointestinal effects such as nausea and diarrhea, though these are reversible and primarily osmotic in nature. PEG 400 is metabolized minimally and rapidly excreted unchanged, primarily in urine, with approximately 40-50% recovery within 24 hours following oral administration in animal and human studies.[56] Its high hydrophilicity prevents bioaccumulation, as it does not bind to tissues and is efficiently cleared via renal pathways.[59] Potential risks from impurities in PEG 400 include residual ethylene oxide, a known carcinogen, and 1,4-dioxane, classified as likely carcinogenic to humans if present above controlled levels.[60] These contaminants arise from the manufacturing process and must be minimized to ensure safety. Potential risks also include ethylene glycol and diethylene glycol, limited to not more than 0.25% combined per USP/NF for PEG 400, with enhanced testing mandated following 2023 FDA alerts on contaminated PEG excipients.[61][62]Regulatory Approvals
Polyethylene glycol 400 (PEG 400) is recognized by the U.S. Food and Drug Administration (FDA) as generally recognized as safe (GRAS) for use as a direct food additive under 21 CFR 172.820, permitting its incorporation in food products at levels consistent with good manufacturing practices.[5] Additionally, PEG 400 is included in the FDA's Inactive Ingredient Database as an approved pharmaceutical excipient for various routes of administration, including oral and topical formulations, with reported maximum concentrations up to 40% in approved drug products to ensure safety and efficacy.[63] In the European Union, PEG 400 is authorized for use in cosmetic products under Regulation (EC) No 1223/2009, listed in the CosIng database as a solvent without a specific maximum concentration limit in Annex III, but subject to stringent purity requirements to minimize impurities such as ethylene oxide and 1,4-dioxane. Under the REACH regulation (EC) No 1907/2006, PEG 400 is registered (EC number 500-038-2) and does not qualify as a substance of very high concern (SVHC), supporting its widespread industrial and consumer applications.[64] The World Health Organization (WHO) acknowledges PEG 400 as an acceptable excipient in pharmaceutical formulations through its technical reports and alignment with international pharmacopeial standards, facilitating its inclusion in essential medicines where low inherent toxicity enables safe use in oral and topical preparations. The United States Pharmacopeia/National Formulary (USP/NF) provides a dedicated monograph for Polyethylene Glycol 400, mandating purity specifications such as heavy metals not exceeding 5 ppm and average molecular weight between 380 and 420 to ensure compliance in medicinal products.[65] As of 2025, global pharmacopeias impose strict limits on residual impurities in PEG 400 to mitigate potential risks, including ethylene oxide not exceeding 10 μg/g (10 ppm) per USP/NF and 1 ppm per European Pharmacopoeia, and 1,4-dioxane not exceeding 10 ppm across major standards like USP/NF and ICH guidelines, with recent enhancements to EG/DEG testing per USP-NF (April 2025) and Ph. Eur. (effective January 2025).[61][66][67] These thresholds require labeling disclosures and testing protocols during manufacturing to verify compliance, reflecting harmonized regulatory efforts for safe excipient use.[68]References
- https://www.sciencedirect.com/topics/[neuroscience](/page/Neuroscience)/polyethylene-glycol