Ansell BIOTAC BioClean Cleanroom Nitrile Gloves Class 100 (ISO 5)

Description
Technical Vault

Ansell BioClean™ BIOTAC Nitrile Cleanroom Gloves (White) — Class 100 (ISO 5) Non-Sterile, Antistatic, EasyTear Packaging

Nitrile Class 100 / ISO 5 Non-sterile Antistatic Textured fingers 12 in / 300 mm 1.5 AQL

BioClean™ BIOTAC nitrile cleanroom gloves are built for controlled-environment handling where operators need reliable chemical resistance, wet grip, and dexterity without introducing avoidable particulate risk. These latex-free, powder-free, ambidextrous white gloves are 300 mm (12”) long for practical wrist coverage, feature a beaded cuff for strength, and use non-particulating EasyTear packaging to reduce entry-related contamination risk.

Why customers choose BIOTAC in ISO 5 work

Nitrile formulation supports comfort, flexibility, and resistance to a range of chemicals for day-to-day cleanroom tasks.
Textured fingers improve wet handling confidence without compromising tactile sensitivity for delicate procedures.
Chlorinated interior promotes smoother donning and helps reduce tackiness during extended wear.
EasyTear inner/outer bag presentation supports cleaner gowning room workflow and controlled dispensing.
SOSCleanroom focuses on best-in-class glove lines for critical environments — we do not compromise glove quality when process yield, contamination control, and operator safety are on the line.

Recommended applications

Cleanroom cleaning and preparing
Chemical handling
Enhanced grip in wet environments
Enhanced tactile sensitivity and dexterity for delicate procedures
Food processing and handling (where non-sterile cleanroom nitrile gloves are appropriate)

Key specifications (from published product details)

SKU	BIOTAC
Cleanroom compatibility	Class 100 / ISO 5
Sterility	Non-sterile
Material	Nitrile
Color	White
Length	300 mm / 12 in
Cuff	Standard length; beaded cuff
Glove shape	Ambidextrous
Surface finish	Textured fingers (external); chlorinated (internal)
Freedom from holes	1.5 AQL (Inspection Level I), Performance Level 2
Thickness (palm)	0.11 mm / 4.33 mil
Thickness (finger)	0.17 mm / 6.69 mil
Antistatic	Yes
Chemo drug testing	Not tested for use with chemotherapy drugs
Case pack	Case (1000 gloves): 100 pieces per sealed inner PE bag; one inner PE bag per sealed outer PE bag; 10 outer bags per lined carton (1000 pieces)

Controlled-environment handling guidance (CCS mindset)

In U.S. cleanroom programs, glove selection and glove-handling discipline are a core element of contamination control strategy (CCS): the right glove reduces particle/chemical transfer risk, but only when it is donned, disinfected, and changed on a defined cadence. If your workflow aligns to FDA expectations for aseptic processing and contamination control, and you reference ISO cleanroom terminology (ISO 14644), BIOTAC supports ISO 5 operations where non-sterile gloves are appropriate. As a global benchmark, EU GMP Annex 1 emphasizes risk-based contamination control and routine glove disinfection/changes in higher-grade areas; use it as an improvement lens without treating it as a U.S. legal requirement.

Gowning room control: Open inner/outer bags deliberately; avoid tearing in turbulent air zones; present gloves for one-at-a-time dispensing.
Disinfection compatibility: Validate compatibility with your site-approved disinfectants/solvents; use published permeation data as a planning tool, not as a safe-wear-time guarantee.
Change discipline: Define glove change triggers (tears, punctures, tacky feel, chemical contact, time-in-use, or after high-contact tasks).
Material transfer: Keep outer surfaces off uncontrolled packaging; stage materials and open bags in a controlled, documented sequence.
Non-sterile note: If your process step requires sterile gloves (e.g., aseptic manipulations inside ISO 5 critical zones under a sterile program), select sterile gloves validated for that operation.

Documentation

Use these references for qualification files, EHS review, and glove selection justification.

SOSCleanroom supports customers who demand best-in-class consumables for critical environments — with fast shipping, excellent customer service, fair pricing, and continuity of supply. If you have any questions please email us at Sales@SOSsupply.com or give us a call at (214)340-8574. If you need additional information please try our SOSCleanroom specific AI ChatBot which draws from our extensive cleanroom specific libraries. Last updated: January 10, 2026 © 2026 SOSCleanroom.com

When Tactile Sensitivity Matters: How Cleanroom Nitrile Gloves Influence Handling Precision, Residue Risk, and ISO 5 Process Stability

The Technical Vault By SOSCleanroom

ISO 14644 Personnel Controls ISO 5 / Class 100 Operations Low-Residue Hand Contact Tactile Control & Dexterity Operator-Induced Contamination

Ansell BioTac™ BioClean™ Cleanroom Nitrile Gloves — what this glove is designed to control

Ansell BioTac™ BioClean™ cleanroom nitrile gloves are designed for Class 100 / ISO 5 and cleaner environments where both contamination control and tactile sensitivity are critical to process outcomes. In many cleanroom workflows, especially precision assembly, optical handling, inspection, and fine cleaning tasks, the glove becomes the dominant interface between the operator and the product.

Gloves that are too thick, inconsistent, or residue-prone can drive handling errors, dropped components, excessive pressure during cleaning, or repeated rework cycles. BioTac™ gloves are typically selected when programs require a balance between low particle contribution and reliable tactile feedback, allowing operators to maintain controlled movements without excessive grip force or repeated contact.

Operations takeaway: In ISO 5 work, glove feel and consistency influence how operators clean, handle, and assemble— which directly affects defect rates and contamination events.

ISO-first context: gloves are a primary contamination control interface

ISO 14644 operations guidance consistently identifies personnel as a primary contamination source. Gloves form the boundary layer between the operator and the controlled environment. Even when garments and air cleanliness are appropriate, glove material, cleanliness, and handling discipline determine whether contamination is transferred to tools, components, or surfaces.

USP-aligned environments reinforce this concept by emphasizing controlled hand contact, defined change intervals, and prevention of residue transfer. Even in non-sterile workflows, glove-derived residues can compromise analytical results, visual inspection outcomes, or cleaning effectiveness.

Technical reference summary (consult current manufacturer documentation for controlled programs)

Product family	Ansell BioTac™ BioClean™
Material	Nitrile (see manufacturer datasheet for formulation details)
Cleanroom compatibility	Class 100 / ISO 5 and cleaner (per product positioning)
Primary use intent	Low-particle, low-residue hand protection with enhanced tactile control
Sterility	Refer to product page and packaging (sterile vs. non-sterile variants)

Quality note: For controlled programs, document glove lot numbers and prohibit substitutions without written approval.

Best-practice use (donning discipline, touch control, and glove change strategy)

Best practice begins with correct donning per your gowning SOP. Hands should be clean and dry prior to donning, and gloves should be pulled on without excessive stretching or snapping, which can generate particles. Once donned, gloves should only contact approved cleanroom surfaces, tools, and materials within the defined work zone.

During precision work, glove behavior directly influences technique. Excess grip force, repeated repositioning, or overhandling can all be signs that glove fit or tactile feedback is suboptimal. Define glove sizes appropriately and discourage extended glove use beyond defined time or task limits, as residue loading and surface changes increase with use.

Establish clear glove change triggers: after contact with non-controlled surfaces, after solvent-heavy tasks, after leaving the controlled zone, or whenever gloves become visibly soiled or compromised. Treat gloves as a consumable contamination control—not as a cost-saving item.

Typical cleanroom failures and how to avoid them (ISO & USP perspective)

Residue transfer during handling: Gloves overloaded or used too long. Prevention: defined change intervals and task-based replacement.
Particles introduced during donning: Poor gowning technique. Prevention: trained donning procedures and audits.
Inconsistent cleaning or assembly results: Loss of tactile feedback. Prevention: proper glove fit and selection.
Unapproved glove substitutions: Changes particle/residue profile. Prevention: lock approved SKUs in SOPs and procurement.
Extended glove reuse: Progressive contamination loading. Prevention: treat gloves as consumables, not durable PPE.

Suggested companion products and technical rationale

Gloves set the baseline for contamination control. Pairing them with compatible swabs, wipers, and cleaning solutions helps maintain method consistency and reduces operator-driven variability.

Suggested swab: Texwipe TX761 Alpha® Polyester Cleanroom Swab — enables precision cleaning while keeping gloved hands away from sensitive surfaces.
Suggested wiper: Texwipe TX1010 Vectra® Alpha® 10 Polyester Cleanroom Wiper — sealed-edge control for surface wipe-downs following handling or swabbing.
Suggested solution: Texwipe TX167 Non-Sterile 70% IPA — supports controlled damp-film cleaning and glove-compatible surface preparation (follow SOPs for sterile workflows).

Disclaimer

This Technical Vault content is provided as supplemental operational guidance only and does not replace manufacturer instructions, facility SOPs, validation protocols, quality risk assessments, or regulatory requirements. Always follow applicable ISO standards, USP chapters, and site-specific procedures. Refer to current manufacturer documentation for sterility status, performance data, and compatibility.