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TX3270 Sterile 70% Isopropanol Alcohol Solution (16 oz.)

Texwipe TX3270 Sterile 70% IPA Isopropanol Alcohol Solution (16 oz.)

$183.80
(No reviews yet)
SKU:
TX3270
Availability:
Stock Item
Shipping:
Calculated at Checkout
Quantity Option (Case):
12 Poly Bottles Per Case (16 Fluid Ounce Trigger Spray Bottles)
Solution Type:
70% Isopropyl Alcohol
Sterile:
Yes

Texwipe TX3270 Sterile 70% IPA Isopropanol Alcohol Solution (16 oz. Trigger Spray)

Texwipe TX3270 is a sterile, ready-to-use 70% isopropanol (IPA / isopropyl alcohol) and 30% USP-purified water solution packaged in fully assembled 16 fl oz (473 mL) trigger-spray bottles. It is designed for contamination-sensitive wipe-downs, pass-through prep, and routine controlled-environment cleaning where consistent wetting, low residue, and lot-level traceability matter. The solution is 0.2 µm filtered, filled in an ISO Class 5 environment, double-bagged in solvent-safe bags, and gamma irradiated to support sterile workflows.

Shipping note: This is a flammable liquid. Ground shipping only (air-freight restrictions may apply).

Specifications:
  • Part number: TX3270
  • Format: Sterile 70% IPA trigger spray (ready-to-use)
  • Composition: 70% by volume USP-grade isopropanol + 30% USP-purified water
  • Filtration / fill: 0.2 µm filtered; filled in an ISO Class 5 environment
  • Sterility assurance: Gamma irradiated to a Sterility Assurance Level (SAL) of 10-6 (per manufacturer documentation)
  • Size: 16 fl oz (473 mL) trigger spray bottle
  • Case pack: 12 poly bottles per case
  • Packaging: Double-bagged in solvent-safe bags
  • Sprayer: Fully assembled; stream delivery or coarse spray
  • % IPA content (typical): 68%–72%
  • NVR (typical): Does not exceed 5 mg in 50 mL (0.01%)
  • Shelf life (sterile): 2 years from date of manufacture
  • Storage conditions: Ambient 59°F to 86°F (15°C to 30°C); keep away from ignition sources
  • Traceability: Individually lot coded with expiration date; Certificates of Compliance/Analysis/Irradiation available (manufacturer certificate center)
About the Manufacturer: 

TX3270 is produced by ITW Texwipe, a contamination-control manufacturer known for controlled filling/packaging practices and documentation discipline that supports qualification workflows. For sterile IPA, the manufacturer positions the product around repeatability and audit readiness: ISO Class 5 filling, 0.2 µm filtration into cleaned containers, double-bagging for controlled entry, and gamma irradiation for sterile-use programs.

 

In day-to-day cleanroom operations, the biggest value is operational consistency: one standard bottle format, one standard spray output, and predictable wetting when paired with compatible low-linting cleanroom wipers (no wiper is truly ‘zero-lint’ in every process condition). SOSCleanroom supports standardization with dependable supply, practical selection guidance, and customer service that understands controlled-environment realities.

TX3270 Features:
  • 70% USP-grade IPA / 30% USP-purified water (by volume)
  • 0.2 µm filtered and packaged into cleaned containers
  • Filled in an ISO Class 5 environment (per manufacturer TDS)
  • Double-bagged in solvent-safe bags for controlled entry
  • Fully assembled trigger sprayer; stream delivery or coarse spray
  • Individually lot coded with expiration date for traceability and recordkeeping
  • Gamma irradiated sterile to SAL 10-6 (per AAMI guidelines, manufacturer documentation)
  • Meets USP <797> and USP <800> requirements (per manufacturer TDS)
  • Meets FDA guideline for medical device bacterial endotoxin limit of not more than 20 EU/device (per manufacturer TDS)
TX3270 Benefits:
  • Process consistency: Ready-to-use sterile IPA reduces variability from in-house mixing, filtration, and bottle assembly.
  • Controlled application: Stream delivery supports precise wetting; coarse spray supports broader wipe coverage.
  • Low residue expectation: Evaporates leaving low residue on compatible surfaces (no rinse required in typical wipe-down use).
  • Audit-ready traceability: Lot coding and manufacturer documentation help support SOPs, batch records, and cleaning logs.
Common Applications:
  • Surface cleaning and residue removal on non-porous cleanroom surfaces
  • Wipe-down for pass-through to controlled environments (when sterile packaging is required by SOP)
  • Glove wipe-downs in sterile suites and controlled environments (per site SOP)
  • Cleaning notebooks, phones, and supplies that enter controlled areas (when allowed by site SOP)
  • Pairing with sterile cleanroom wipers for critical wipe-down steps
Best-Practice Use:
  • Spray onto the wipe for critical work: In high-sensitivity areas, wet a compatible low-linting cleanroom wiper first to reduce overspray and airborne droplets.
  • Use a disciplined wipe pattern: Wipe in one direction with overlapping strokes; rotate to a fresh wipe face frequently to avoid re-depositing contaminants.
  • Two-pass cleaning when needed: First pass lifts soils/residue; second pass supports a cleaner finish (as required by your process).
  • Compatibility check: Confirm compatibility with plastics, elastomers, coatings, and adhesives before broad deployment.
  • Cleaning vs. disinfection: IPA is widely used for cleaning and residue removal; for validated disinfection/sporicidal control, follow your site-approved disinfectant rotation and required wet-contact times.

Safety reminder: Highly flammable liquid and vapor. Use in a well-ventilated area, keep away from ignition sources, and follow your site PPE and EHS program. Refer to the current SDS for full hazard, handling, and disposal guidance.

Selection Notes (TX3270 16 oz. Sterile Trigger Spray vs. Other Options)
  • Sterile vs. non-sterile IPA: Choose sterile when your SOP requires sterile packaging, irradiation documentation, and sterile-use workflows (e.g., USP <797> / <800> contexts).
  • Trigger spray vs. bulk bottles: Trigger sprays support controlled, repeatable application; bulk formats can be preferred for higher-volume wetting or refill programs (where permitted by SOP).
  • 70% vs. higher concentration alcohol: 70% IPA is commonly selected for routine wipe-downs and residue removal; higher concentrations are typically chosen when required by process needs and material compatibility.

Notes: Need help standardizing sterile IPA for pass-through wipe-downs, glove wipe steps, or routine controlled-environment cleaning? Contact SOSCleanroom for practical selection guidance based on surfaces, residues, and workflow constraints—including compatible low-linting wipers and dispensing best practices.

SOSCleanroom.com supports contamination-control programs with dependable supply, fair pricing, and responsive support backed by customer service that understands real cleanroom workflows.

Product page updated: Jan. 7, 2026 (SOS Technical Staff)

© 2026 SOS Supply. All rights reserved.

The Technical Vault Sterile 70% IPA · Routine/Intermediate Disinfection Support · Clean Entry Packaging

Texwipe TX3270 Sterile 70% IPA Isopropanol Alcohol Solution (16 oz. Trigger Spray)

Texwipe TX3270 is a sterile, ready-to-use solution of 70% isopropanol (IPA) and 30% USP-purified water, packaged in fully assembled 16 fl oz (473 mL) trigger-spray bottles. It is commonly used for contamination-sensitive wipe-downs, pass-through prep, and routine controlled-environment cleaning where consistent wetting, low residue, and lot-level traceability matter.

At-a-glance (published attributes)
  • Solution type: 70% Isopropyl Alcohol (IPA) / 30% USP-purified water
  • Format: Fully assembled trigger-spray bottle, 16 fl oz (473 mL)
  • Case pack: 12 poly bottles per case
  • Sterility: Yes (sterile product)
  • Filtration / packaging notes: 0.2 µm filtered; double-bagged for clean entry (as listed on the product page)
  • Shipping constraint: Ground shipping only (flammable / ORM-D acknowledgement on checkout workflow)

1) Where TX3270 fits in a contamination control program

Sterile 70% IPA is widely used as a routine or intermediate disinfectant step in ISO-classified environments. In practice, it is used to: (a) support frequent wipe-down of cleanroom contact surfaces, (b) prep items for controlled entry (e.g., pass-through staging), and (c) sanitize gloved hands during operations, when defined in the facility SOP.

Important scope note (accuracy-first)

70% IPA is not a sporicide. Many validated programs use IPA for routine/intermediate disinfection and implement a separate sporicidal agent on a defined schedule as part of a rotation. Always follow your site’s contamination control strategy and validation protocol.

2) Standards alignment (USP, ISO, Annex 1) — educational reference

In critical environments, standards and guidance consistently emphasize: (1) the need for clean and disinfected surfaces, (2) trained personnel using appropriate garb/PPE, and (3) documented, validated procedures. USP <797> and USP <800> expect cleaning/disinfection activities to be controlled through SOPs using suitable agents and appropriate PPE for the task. EU GMP Annex 1 reinforces the need for a robust contamination control strategy, including validated disinfection processes and disciplined operator behavior. ISO cleanroom operations guidance (e.g., ISO 14644-5) supports establishing an operations control program covering personnel practices, cleaning, and material movement.

Key compliance reality: these frameworks do not “approve” a specific brand or bottle style. Facilities are responsible to select, validate, document, and train on the exact products and methods used in their rooms.

3) Application technique (what auditors look for)

A. Prefer “spray-to-wipe,” not “spray-to-surface” (when feasible)

For many critical surfaces, applying IPA onto the wiper (then wiping) improves control of saturation and reduces aerosolization and overspray. Where your SOP allows direct spray on a surface, define the target area, spray distance, and maximum wetting to prevent pooling or drip transfer.

B. Single-pass, unidirectional wiping with overlap

Use single-pass strokes (do not “scrub back and forth” with the same face of the wiper). Overlap strokes to avoid missed lanes. Change to a clean wiper face (or a new wiper) as soon as it becomes loaded, dries out, or contacts a non-controlled surface.

C. Contact time is defined by your SOP and validation

Maintain the surface visibly wet for the contact time specified in your procedure. Contact time and technique should be validated for the way your team actually uses the product (surface type, wiping method, and environmental conditions).

4) Donning discipline and PPE interface control

Cleaning and disinfection should be performed by trained, appropriately garbed personnel. A common failure mode in audits is not the chemical—it’s touch events (adjusting eyewear, re-touching non-controlled objects, poor glove-sleeve overlap) that reintroduce contamination.

Practical, SOP-aligned reminders
  • Be fully gowned before introducing sterile solutions into ISO-classified areas.
  • Don sterile gloves last (typical practice), then sanitize gloves with sterile IPA per SOP.
  • If you must adjust goggles/hood/mask, follow your SOP (e.g., re-sanitize gloves, replace PPE, or step out).
  • Confirm PPE needs for splash risk (eye protection) and chemical exposure (e.g., USP <800> hazardous drug handling).

5) System pairings (to standardize performance)

TX3270 is typically most effective when paired with cleanroom consumables engineered for low residue transfer and controlled wiping. Below are common pairings used in validated programs (final selection must match your ISO class, room behavior, and SOP validation):

6) Selection notes (why this 16 oz sterile trigger format)

  • Repeatable dosing: trigger format supports consistent surface wetting when the spray pattern and distance are standardized in SOP.
  • Clean entry readiness: double-bagging supports staged de-bagging for controlled introduction.
  • Operational efficiency: assembled bottles reduce setup steps and variability across shifts.
  • Traceability: sterile solutions are commonly managed with lot-level traceability in validated programs.

7) Safety and handling (non-negotiables)

Flammability & SDS

70% IPA is a highly flammable liquid and vapor. Use in a well-ventilated area, keep away from ignition sources, and follow your site’s PPE and EHS program. Always refer to the current SDS for full hazard, handling, storage, and disposal guidance.

Revision control

Technical Vault entry (SOSCleanroom): This content should be reviewed whenever manufacturer documentation, USP chapters, ISO standards, or Annex 1 guidance is revised, or whenever your site changes cleaning SOPs or validation parameters.

Disclaimer: This Technical Vault content is provided for educational and reference purposes only. It does not constitute regulatory, quality, engineering, environmental health & safety, or legal advice. Cleaning agents, contact times, wiping techniques, PPE requirements, disinfectant rotation, and all related procedures must be defined, validated, and documented by the end user in accordance with internal SOPs, risk assessments, and applicable standards and regulations. Always follow manufacturer instructions and the current SDS.

© 2026 SOS Supply. All rights reserved.