Ansell Gloves

How to select correctly

Define what must be protected before choosing an Ansell product.

Ansell is not one glove category. Its portfolio includes sterile cleanroom gloves, processed nonsterile gloves, examination gloves, chemical-protective gloves, knitted cut-resistant gloves and fixed isolator glove assemblies. Each serves a different combination of product protection, operator protection and functional performance.

Start with the task

Ansell glove selection matrix for critical environments and industry.

This matrix provides candidate products, not a declaration of suitability. Facility assessment, governing chapters, manufacturer reports and actual-use testing determine final approval.

Brand architecture

Understand the Ansell families before comparing model numbers.

For a broader manufacturer catalogue view, use the SOSCleanroom Ansell Brochures & Technical Library and the Ansell BioClean official portfolio.

Material science

Nitrile, neoprene, polyisoprene and latex are not equivalent barriers.

Technical literacy

Nine glove claims buyers should never treat as interchangeable.

The exact product data sheet and revision are more reliable than an abbreviated catalog title. A nonsterile ISO 4 glove is not an alternative to a sterile ISO 5 glove when sterile handling is mandatory.

Aseptic manufacturing and compounding

Sterile BioClean and TouchNTuff are selected by the entire sterile workflow.

Sterile hand protection begins with the documented sterile barrier, but success also depends on operator behavior. Ansell markets Ansell BioClean Excell BEXS and Ansell BioClean Emerald BENS within its BioClean sterile nitrile portfolio. Another candidate is Ansell TouchNTuff 93-700 for sterile Class 100 / ISO 5 applications. These are examples for evaluation rather than automatic substitutes.

Explore the SOSCleanroom Sterile Nitrile Gloves category and the Ansell BEXS manufacturer data sheet hosted by SOSCleanroom.

Controlled manufacturing

Nitrilite and cleanroom MICROFLEX are useful only when process qualification supports them.

In nonsterile controlled processes, the glove may be chosen for cleanliness, electrostatic behavior, packaging and operator dexterity rather than microbial sterility. Ansell Nitrilite 93-311 and Ansell Nitrilite 93-401 are Nitrilite examples listed for distinct cleanroom-use contexts; Ansell MICROFLEX CE5-755 is another nonsterile cleanroom-nitrile candidate.

Latex sensitivities and gowning

Compare neoprene, synthetic polyisoprene and latex without unsupported allergy claims.

Where natural-rubber latex allergies or sensitivity risks matter, Ansell has sterile polychloroprene and synthetic polyisoprene alternatives. However, formulations and accelerator claims differ by model; do not use a material family as proof of an "allergy free" glove.

Check whether a model is hand-specific or ambidextrous, whether the cuff is beaded or straight, and how the glove behaves through full arm extension. A nominal "12-inch" description should not replace actual gown-interface testing.

Pharmacy and life sciences

USP 795, USP 797 and USP 800 answer different glove questions.

For a complete facility program, use the SOSCleanroom USP 797 Compliance Guide, USP 800 Hazardous Drug Handling Guide and Cleanroom Glove Selection Guide.

Hazardous-drug exposure

Chemotherapy glove testing is drug-specific; double-gloving is not optional in HD compounding.

Permeation is chemical movement through an intact glove. Penetration means passage through a physical defect or opening; degradation refers to changes in the material. An ordinary nitrile glove and an ASTM D6978-tested chemotherapy glove cannot be treated as equivalent just because both are blue nitrile.

Ansell candidates include Ansell BioClean Emerald BENS, Ansell TouchNTuff 93-700 and Ansell TouchNTuff DermaShield 73-701 where model-specific documentation supports ASTM D6978. Verify the actual drug list; a sterile product without that test claim must not be marketed as universally chemotherapy protective.

Primary references: USP 800 January 2026 FAQ, ASTM D6978-05(2023) standard listing and CDC/NIOSH hazardous-drug reference.

High-use disposable programs

MICROFLEX exam-glove selection should prioritize fit and actual barriers.

MICROFLEX supplies disposable glove choices for laboratories, medical examination and production support areas where operators may need high tactile sensitivity and frequent glove changes. Products such as Ansell MICROFLEX XCEED XC-310, Ansell MICROFLEX 93-260 and Ansell MICROFLEX MidKnight 93-732 address different tradeoffs; none should be assumed sterile merely because the line is used in a healthcare setting.

Chemical protection

AlphaTec and chemical-resistant MICROFLEX require exposure-specific selection.

AlphaTec addresses hazards where conventional cleanroom or exam gloves may not offer suitable chemical protection. The Ansell AlphaTec Solvex 37-155 product is an unflocked reusable nitrile chemical-handling model. Unflocked construction can matter in some support operations, but it is not proof of cleanroom qualification. For selected disposable chemical tasks, Ansell MICROFLEX 93-260 may be evaluated separately.

For chemical exposure assessment, consult Ansell chemical selection support and OSHA hand protection guidance. Chemical-specific compatibility data should be reviewed before use.

Cut, abrasion and grip

HyFlex belongs to mechanical-hazard programs, not automatic cleanroom gowning.

HyFlex gloves serve a different safety need: cut, abrasion, grip, precision assembly and selected electrostatic control. They are generally knitted industrial products rather than sterile, pair-packed disposable cleanroom gloves. Match the actual mechanical hazard and model revision to the employer PPE program.

The dedicated SOSCleanroom HyFlex Guide examines ANSI/ISEA 105 and EN 388, coated-knit limitations, grip, oil exposure, ESD and model-specific specification changes in greater depth.

Microelectronics and ESD

An electrostatic claim does not certify the total cleanroom or ESD program.

Static can attract particles and damage sensitive electronic components, but electrostatic performance must be assessed as a system. Even an industrial glove marketed as ESD-safe can have an unsuitable particle or residue profile for an exposed wafer, optical component or device.

Closed-barrier systems

RABS and isolator gauntlets need equipment-specific qualification and integrity testing.

Fixed gloves used in restricted access barrier systems and isolators are engineered components of the equipment barrier. Ansell BioClean GGL sterile isolator glove and Ansell BioClean CGL clean isolator glove are separate sterile and clean BioClean product concepts. They should not be treated as interchangeable with a disposable hand glove or with each other.

See Ansell RABS and isolator documentation and Ansell biopharma portfolio overview for model-family context. Use equipment- and lot-specific information for purchase approvals.

Contamination control

Particle, ion and extractable risk must be evaluated apart from sterile status.

Gloves are high-frequency contact surfaces. In a semiconductor or optical environment, transfer of particles, fibers, nonvolatile residue, ions, silicone or chemical additives can matter more than nominal glove thickness. In pharmaceutical aseptic work, loss of sterility through poor handling or compromised packaging is a different but equally important control failure.

Ergonomics and barrier integrity

Fit influences dexterity, cuff coverage, fatigue and glove failure.

Glove selection fails when sizing is treated as an afterthought. A tight glove can fatigue hands and be more difficult to don safely; loose fingertips can catch on small fittings, stoppers, microscope controls and small components. Test glove sizes with the tools, movements and double-glove arrangements actually used.

Use the SOSCleanroom Glove Sizing Chart when planning operator samples and approved size profiles.

People and process

Donning, disinfection, glove changes and doffing require distinct SOPs.

Gowning and removal should preserve both product cleanliness and worker safety. Build distinct procedures for sterile work, routine nonsterile lab work, hazardous-drug handling, and reusable industrial chemical gloves. The correct sequence is not universal across those environments.

Sterile 70% isopropyl alcohol is used on gloves during USP <797> compounding under the chapter, but disinfection does not mend a torn glove or neutralize all hazardous-drug residues. Glove changes must consider integrity and contamination, not only elapsed time.

Audit-ready records

Build a glove qualification file tied to exact models and lots.

A product listing is helpful for screening, but a controlled program needs documentary evidence that survives a product change, inspection or contamination investigation. Different families require different documentation; not all glove styles provide certificates of irradiation or pharmaceutical-specific certificates.

Helpful manufacturer access: Ansell Certificates Portal, Ansell BioClean portfolio, and SOSCleanroom Ansell Brochures.

Direct catalog destinations

Compare 23 exact Ansell glove listings on SOSCleanroom.

These are direct SOSCleanroom product listings, not broad category shortcuts. Selection examples are not blanket approvals, regulatory certifications, or guarantees of chemical compatibility. Follow the product page for current pack formats, variant options, availability and manufacturer documentation.

For the full Ansell assortment, use Ansell Gloves category, Sterile Nitrile Gloves, Ansell Exam Gloves and Industrial Gloves.

Application examples

What changes when the customer works in pharmacy, chips, biotech or industrial maintenance?

Eight-step program

Turn a glove purchase into a document-controlled qualification decision.

Purchasing and supply continuity

Specify what you really need before accepting substitutions.

Matching a unit price without comparing sterile presentation, contamination controls, change frequency and qualified waste is not a meaningful total-cost comparison. Ask about SOSCleanroom B2B purchasing programs once the approved products and sizes have been identified.

Troubleshooting

Recognize glove selection failures before they become quality or exposure events.

Frequently asked questions

Technical answers to the most common Ansell glove selection questions.

Continue your learning

Connect Ansell selections to the SOSCleanroom knowledge base.

Source basis and verification

Authoritative Ansell, USP, OSHA, NIOSH, ASTM and EU GMP references.

Manufacturer PDFs and commercial websites are subject to revision, and some standards require paid access. Consult the current official publications and the specific lot/model documentation before changing approved procedures. This guide is a selection aid, not legal, clinical, compliance or PPE certification advice.

SOSCLEANROOM  |  ANSELL GLOVE PROGRAMS & B2B SOURCING

Choose a Glove You Can Specify, Qualify & Reorder with Confidence.

Tell SOSCleanroom your application, sterile or cleanroom needs, chemical or hazardous-drug exposure, preferred material, sizes, annual usage and documentation requirements. We can help identify candidate Ansell products and sourcing options, while your QA, pharmacy, EHS and engineering teams retain final qualification authority.

Contact: 800-443-7101  |  Sales@SOSsupply.com