Key takeaways

Choosing the Right AHAM Testing Path

  1. Use AHAM AC-1 when the decision depends on CADR, smoke, dust, pollen, room-size guidance, or particulate clean-air delivery.
  2. Use AHAM AC-5 when the decision depends on experimentally generated bioaerosol reduction and viability in an aerobiology test chamber.
  3. Use ASHRAE 241 as the building and air-cleaning effectiveness frame, then select the test method that fits the device, claim, and authority having jurisdiction.
  4. Do not treat a particulate CADR result as a stand-alone microorganism, infection-risk, or public-health claim without checking the claim and regulatory context.

Start with the decision each standard answers

AHAM AC-1 and AHAM AC-5
In this article, AHAM AC-1 refers to the ANSI/AHAM standard for room-air-cleaner CADR and particulate performance. AHAM AC-5 refers to the ANSI/AHAM standard for assessing how quickly portable air cleaners reduce key bioaerosols in an aerobiology test chamber.1,2,4

AHAM is an accredited standards development organization. Its performance standards provide common methods for testing home appliances and reporting major performance attributes. For room air cleaners, AHAM lists ANSI/AHAM AC-1-2020 for CADR and ANSI/AHAM AC-5-2023 for bioaerosol performance.1

The practical distinction is the type of evidence each standard provides. AC-1 addresses clean-air delivery for nonbiological particulate challenges. AC-5 addresses bioaerosol reduction, including changes in concentration and viability. Both standards may inform filtration efficiency discussions, but their results should not be combined into a single generic air-cleaner claim.3,4,8

What AHAM AC-1 shows

AHAM Verifide defines CADR as the volume of filtered air delivered by an air cleaner and reports separate scores for tobacco smoke, pollen, and dust. Within the AHAM framework, a higher CADR for a listed pollutant indicates faster filtration of that pollutant. AHAM's consumer guidance also uses CADR to help select an air cleaner for a given room size.3

EPA states that it does not certify, register, recommend, or publish lists of acceptable air-cleaning devices, although it identifies AHAM as one source of information. EPA also notes that AHAM's air-cleaner certification program is known as AC-1. For that reason, AC-1 evidence is generally described as third-party performance verification, not EPA endorsement.9

CDC's ventilation FAQ treats CADR as a clean-air input for portable HEPA air cleaners. It explains that AHAM labels report smoke, dust, and pollen CADR values. Of those values, CDC identifies smoke CADR as the most relevant to viral particles associated with respiratory diseases because smoke is the smallest listed AHAM challenge particle.10

What AHAM AC-5 shows

AHAM's current AC-5 item page describes ANSI/AHAM AC-5-2023 as a method for measuring how quickly portable air cleaners reduce key bioaerosols in an aerobiology test chamber. The standard is intended to evaluate the ability of portable household air cleaners to reduce the concentration and viability of experimentally generated bioaerosols within a specified chamber.4

When AHAM announced the earlier AC-5 edition, it described the method as its first air-cleaner performance standard focused on microbiological pollutants, including viruses, bacteria, and mold. This purpose differs from AC-1. AC-5 applies when the study question concerns bioaerosol reduction rather than particulate CADR, room sizing, or CADR-to-watt efficiency alone.4,5,11

For compliance planning, AC-5 testing does not replace a review of the proposed claim language. EPA includes air purifiers, filters, and air treatment devices among examples of regulated devices when they claim to reduce microorganisms or purify the air. EPA also notes that HEPA filters limited to particle-size claims, without air-purification or microorganism claims, are generally outside FIFRA device regulation.8

How ASHRAE 241 uses AHAM methods

ASHRAE describes Standard 241 as establishing minimum requirements intended to reduce disease-transmission risk from exposure to infectious aerosols in new buildings, existing buildings, and major renovations. It therefore provides a risk-mitigation framework for buildings and air systems, not a stand-alone certification program for air cleaners.6

ASHRAE Addendum a to Standard 241-2023 identifies ANSI/AHAM AC-1 and ANSI/AHAM AC-5 as consensus standards that may be used to determine air-cleaning effectiveness when the method is appropriate for the system and accepted by the authority having jurisdiction. The addendum also states that commercial and industrial in-room air cleaners using only mechanical fibrous filters determine equivalent clean airflow rate using ANSI/AHAM AC-1, adapted for nonresidential applications according to the specified chamber-size criterion.7

How AC-1, AC-5, and ASHRAE 241 differ3,4,6,7,8
FrameWhat it showsWhat it does not decide alone
ANSI/AHAM AC-1Portable room-air-cleaner CADR for particulate challenges such as smoke, dust, and pollen.Bioaerosol viability, microorganism claim support, ozone safety, or installed HVAC performance.
ANSI/AHAM AC-5Bioaerosol reduction rate, concentration reduction, and viability reduction in a specified aerobiology chamber.Particulate CADR room-size labeling, CADR-to-watt efficiency, or all public-health claim obligations.
ASHRAE 241A building and air-cleaning effectiveness framework for infectious-aerosol risk mitigation.Product approval, EPA device compliance, or automatic acceptance of any one laboratory report.

Scoping questions before testing

  • Name the decision first: particulate CADR comparison, bioaerosol reduction, ASHRAE 241 equivalent clean airflow, EPA claim support, or engineering screening.3,4,7,8
  • Define the product configuration: portable household room air cleaner, larger in-room commercial device, ducted HEPA unit, in-duct UV system, HVAC filter, or custom recirculating system.7,10
  • Separate particle removal, filter efficiency, bioaerosol viability, ozone or byproduct safety, and energy-efficiency questions before writing the protocol.3,4,10,11
  • Check whether marketing language reaches microorganisms, air purification, pathogen mitigation, or public-health outcomes, because those words can change the EPA device and evidence discussion.8,9

Practical questions

Q.Is AHAM AC-1 the same as AHAM AC-5?
A.No. AHAM AC-1 provides the CADR and particulate-performance framework for portable room air cleaners. AHAM AC-5 provides the bioaerosol reduction-rate framework for portable household air cleaners tested in an aerobiology chamber.
Q.Does an AC-1 CADR result prove bioaerosol inactivation?
A.Not by itself. AC-1 CADR measures clean-air delivery for particulate challenges such as smoke, dust, and pollen. AC-5 is the AHAM method for evaluating reductions in the concentration and viability of experimentally generated bioaerosols.
Q.How does ASHRAE 241 use AHAM standards?
A.ASHRAE 241 is a building and air-system standard for mitigating risks associated with infectious aerosols. Addendum a allows ANSI/AHAM AC-1 and ANSI/AHAM AC-5 to be used as consensus standards for determining air-cleaning effectiveness when the method fits the system and is accepted by the authority having jurisdiction.
Q.When does EPA pesticide-device context matter?
A.EPA context becomes important when an air purifier, filter, UV unit, or other air treatment device claims to reduce microorganisms, purify the air, or mitigate pests. EPA notes that HEPA filters limited to particle-size claims, with no air-purification or microorganism claims, are generally outside FIFRA device regulation.
Q.Which AHAM result is most useful for respiratory-particle room sizing?
A.CDC explains that AHAM labels report separate smoke, dust, and pollen CADR values. CDC considers smoke CADR the most applicable of these values to viral particles associated with respiratory diseases because smoke is the smallest of the listed AHAM challenge particles.
Q.What should be provided before scoping AHAM-related testing?
A.Helpful scoping information includes the device type, operating mode, intended claim, target standard, and whether the project requires particulate or bioaerosol evidence. The study team should also define the chamber or installed configuration, airflow basis, safety considerations, and whether the report will support ASHRAE 241 calculations, EPA claim review, procurement, or engineering screening.
Next step

Discuss testing context

Use the article as a starting point, then bring product, device, formulation, claim, or regulatory context into a project scoping conversation.

Request a quote

Why ARE Labs

ARE Labs connects technical topics to practical study design, method selection, controlled aerosol work, and reportable evidence without turning technical pages into sales pages.

Reviewed byJamie Balarashti (25 yrs - cascade & inhalation methods) - Weston Schaper (7 yrs - real-time sizing & nanoparticle work)
QualityDocumented study records
900+Studies Performed
17+Years in operation
300+Clients supported
Testing relevance

How ARE Labs scopes AHAM-related testing

ARE Labs uses the intended claim, device configuration, standard, target aerosol, chamber condition, airflow basis, and reporting goal to choose between CADR, filtration efficiency, bioaerosol reduction, ASHRAE 241 support, and air-device safety testing.

Primary ARE Labs test paths

Related ARE Labs links