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What is Acetal Also Known As? A Guide to Polyoxymethylene (POM)

4 min read

Over 95% of applications can use either of the two main types of acetal plastic, a versatile engineering thermoplastic [1.5.2]. Acetal is chemically known as Polyoxymethylene (POM) and is also referred to as polyacetal and polyformaldehyde [1.2.2].

Quick Summary

Acetal is a high-strength, low-friction engineering thermoplastic chemically known as Polyoxymethylene (POM) [1.2.1, 1.2.2]. It exists in homopolymer and copolymer forms and is used for precision parts in various industries, including medical devices.

Key Points

  • Alternate Names: Acetal is chemically known as Polyoxymethylene (POM), polyacetal, and polyformaldehyde [1.2.2].

  • Two Main Types: It comes in two primary forms: homopolymer (POM-H), like Delrin®, and copolymer (POM-C), like Celcon® [1.2.1, 1.2.7].

  • Homopolymer Strengths: POM-H offers higher stiffness, tensile strength, and creep resistance [1.2.1].

  • Copolymer Advantages: POM-C has better chemical resistance, less porosity, and is preferred for medical/food applications [1.2.5, 1.2.7].

  • Chemical Definition: In chemistry, an acetal is a functional group with a carbon atom single-bonded to two oxygen atoms [1.3.1].

  • Formation: Acetals are formed by reacting an aldehyde or ketone with an excess of alcohol in the presence of an acid catalyst [1.7.1].

  • Medical Uses: In pharmacology, acetal is used for drug delivery devices like insulin pens, surgical instruments, and prosthetics [1.6.3, 1.6.4].

  • Key Properties: Acetal is valued for high strength, low friction, excellent dimensional stability, and low moisture absorption [1.2.6, 1.3.2].

In This Article

Understanding Acetal: Beyond the Name

Acetal is an engineering thermoplastic widely utilized for precision components that demand high stiffness, low friction, and exceptional dimensional stability [1.2.6]. But what is acetal also known as? Its formal chemical name is Polyoxymethylene, frequently abbreviated as POM [1.2.3]. It may also be referred to as polyacetal or polyformaldehyde [1.2.2]. This material is a staple in engineering due to its well-rounded characteristics, making it suitable for applications in wet environments and for parts requiring high strength and stiffness [1.2.1]. The polymer is created from formaldehyde, and its discovery is credited to German chemist Herman Staudinger, though it wasn't commercialized until the 1960s due to initial issues with thermal stability [1.5.5].

Acetal's structure is semi-crystalline, which contributes to its intrinsic opaque white appearance, high strength, and hardness at temperatures as low as -40°C [1.2.2]. This structure means it has a sharp melting point rather than gradually softening with heat, transitioning quickly from a solid to a low-viscosity liquid [1.5.3]. This property is advantageous for manufacturing processes like injection molding and extrusion [1.2.2].

The Two Faces of Acetal: Homopolymer vs. Copolymer

Acetal is primarily produced in two formulations: homopolymer (POM-H) and copolymer (POM-C) [1.2.1]. While they can be used interchangeably in most applications, key differences in their structure and properties make them suitable for specific uses [1.5.2].

  • Acetal Homopolymer (POM-H): This type is formed by the polymerization of formaldehyde directly [1.5.5]. It is known for having higher crystallinity, which results in better mechanical properties like higher tensile strength, stiffness, creep resistance, and hardness compared to the copolymer [1.2.1, 1.5.2]. A well-known trade name for POM-H is Delrin®, manufactured by DuPont [1.2.1, 1.2.7]. However, a significant disadvantage of POM-H is its potential for centerline porosity—microscopic voids in the center of the material, especially in thicker sections. This can be a concern in applications where a uniform, solid structure is critical [1.2.4, 1.2.5].

  • Acetal Copolymer (POM-C): This type is created by polymerizing trioxane (derived from formaldehyde) along with a co-monomer [1.5.5, 1.2.2]. This structure gives it superior chemical resistance, especially to hot water and high pH solutions, better dimensional stability, and less outgassing during machining compared to the homopolymer [1.2.1, 1.2.7]. Crucially, POM-C is largely free of the centerline porosity found in POM-H, making it the preferred choice for medical and food-contact applications [1.2.5, 1.2.2]. Common trade names include Celcon® and Hostaform® [1.2.5].

Feature Acetal Homopolymer (POM-H) Acetal Copolymer (POM-C)
Mechanical Strength Higher tensile strength and stiffness [1.2.7] More flexible, higher impact resistance [1.5.1]
Porosity Prone to centerline porosity [1.2.4] Little to no centerline porosity [1.2.5]
Chemical Resistance Good Better, especially to high pH and hot water [1.2.7]
Thermal Stability Lower processing window Wider processing window, less outgassing [1.2.2]
Common Trade Name Delrin® [1.2.7] Celcon®, Hostaform® [1.2.5]
Primary Application High-strength gears, structural parts [1.5.2] Medical and food-contact parts [1.2.5]

The Chemistry of Formation and Protection

In organic chemistry, the term 'acetal' refers to a functional group where a central carbon is bonded to two ether (-OR) groups [1.4.3]. These are formed when an aldehyde or a ketone reacts with an excess of alcohol in the presence of an acid catalyst [1.7.1]. This reaction is reversible and proceeds through an intermediate stage called a hemiacetal, which has one -OR group and one hydroxyl (-OH) group on the same carbon [1.7.1, 1.4.4].

The reversibility of this reaction is crucial. To form an acetal, water must be removed from the mixture to drive the reaction forward [1.7.4]. Conversely, to break an acetal apart (hydrolysis), one can add excess water in the presence of an acid catalyst, which regenerates the original aldehyde or ketone and alcohol [1.7.2]. This property makes acetals excellent 'protecting groups' in organic synthesis. They can be used to shield a carbonyl group from reacting while other parts of a molecule are modified, and then be easily removed [1.7.5].

It's important to distinguish acetals from ketals. Historically, 'acetal' was used for derivatives of aldehydes, and 'ketal' for derivatives of ketones. Under current IUPAC nomenclature, 'acetal' is the general term for both, but 'ketal' is still acceptable as a subclass of acetals derived specifically from ketones [1.4.1, 1.4.2].

Acetal in Pharmacology and Medical Applications

Acetal's unique combination of properties—biocompatibility, sterilizability, strength, and low friction—makes it a valuable material in the medical and pharmaceutical fields [1.6.6].

Key Medical Uses:

  • Drug Delivery Devices: Low-friction grades are used in components for devices like insulin pens and metered-dose inhalers, ensuring smooth and accurate dose delivery [1.6.4, 1.6.5].
  • Surgical Instruments: Its ability to withstand repeated sterilization makes it ideal for handles, trays, and various components of surgical and dental instruments [1.6.1].
  • Prosthetics: The material's durability and built-in lubricity are beneficial for functional parts in prosthetic feet, elbows, and knee joints [1.6.3].
  • Diagnostic and Imaging Equipment: Components in MRI machines, endoscopic probes, and handheld diagnostic wands are often made from acetal due to its dimensional stability and chemical resistance [1.6.1].

Medical-grade acetal copolymers, such as Celcon® M25, are specifically formulated and tested for contact with blood and tissue [1.2.7, 1.6.2]. The lack of porosity in copolymers is a key reason for their preference in these sensitive applications [1.2.5].

Conclusion

So, what is acetal also known as? It is most commonly known by its chemical name, Polyoxymethylene (POM), and by famous trade names like Delrin® and Celcon® [1.2.6, 1.2.7]. This versatile engineering thermoplastic is far more than just a plastic; its distinct homopolymer and copolymer forms offer a range of properties tailored for specific needs. From high-performance gears in cars to life-saving components in medical devices, acetal's strength, low friction, and stability have cemented its role as a critical material in modern manufacturing and pharmacology. Its ability to be precisely machined and its resistance to chemicals and moisture ensure its continued use in demanding applications where reliability is paramount [1.3.2].


For more information on the chemical compatibility of Acetal (POM), you can refer to resources provided by industrial suppliers such as the Industrial Specialties Mfg. (ISM) blog. [1.2.5]

Frequently Asked Questions

The most common trade names depend on the type. For acetal homopolymer (POM-H), the most widely known trade name is Delrin®. For acetal copolymer (POM-C), common names include Celcon® and Hostaform® [1.2.1, 1.2.5].

Delrin® is a specific brand name for an acetal homopolymer (POM-H). 'Acetal' is the general term that refers to both homopolymer (POM-H) and copolymer (POM-C) materials [1.3.2].

The chemical name for acetal plastic is Polyoxymethylene, often abbreviated as POM. It is also sometimes called polyacetal or polyformaldehyde [1.2.3, 1.2.2].

Homopolymer (POM-H) has higher mechanical strength and hardness. Copolymer (POM-C) has better chemical resistance, superior dimensional stability, and is not prone to the centerline porosity that can be found in homopolymers, making it better for medical applications [1.2.1, 1.2.5].

Yes, specific medical-grade acetal resins are used in medical devices. Acetal copolymers are often preferred due to having little or no porosity and can be sterilized repeatedly. They are used in surgical instruments, prosthetics, and drug delivery devices [1.2.7, 1.6.1, 1.6.3].

An acetal has a carbon atom bonded to two -OR (ether) groups. A hemiacetal, which is an intermediate in acetal formation, has one -OR group and one -OH (hydroxyl) group attached to the same carbon [1.7.1].

Acetal is used in pharmacology and medical devices for its high strength, low friction (lubricity), chemical resistance, dimensional stability, and ability to be sterilized. These properties are ideal for precision parts in devices like insulin pens and inhalers [1.6.3, 1.6.4, 1.6.6].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.