In a controlled environment, “70% IPA” sounds interchangeable until you are the person explaining a residue streak, a missing lot record, or a compromised clean-entry step during an audit. TX3270 is built for the day-to-day reality of cleanroom wipe-down: predictable composition, sterile presentation, lot traceability, and packaging that supports disciplined pass-through and point-of-use handling.

This SKU is a ready-to-use sterile 70% isopropanol solution in an assembled 16 fl oz trigger spray bottle, intended to reduce in-house variability (mixing, filtration, bottle assembly) and tighten the documentation trail for routine cleaning tasks.

• Surface cleaning and residue removal on compatible non-porous surfaces (benches, carts, trays, pass-through items).
• Wipe-down of items entering controlled environments where sterile packaging and lot traceability are required.
• Glove wipe-downs in sterile suites when permitted by your facility’s SOP and risk assessment.
• Routine cleaning workflows where low residue and repeatability matter more than “whatever alcohol is available.”

• Sterile, ready-to-use control: avoids in-house blending and bottle handling that can introduce variability and documentation gaps.
• Clean-entry packaging: double-bagged packaging supports controlled introduction into critical areas.
• Process and audit readiness: lot-coded bottles with expiration dating support recordkeeping; manufacturer documentation supports lot-level certification workflows.
• Spray discipline: adjustable output (stream/coarse spray) helps reduce overspray risk while still covering large wipe-downs efficiently.
• Partnership reliability: SOSCleanroom maintains a close working relationship with ITW Texwipe to support continuity of supply, documentation handoff, and practical application guidance for customers standardizing cleanroom solutions.

The solution is a blend of 70% by volume USP-grade isopropanol and 30% USP-purified water. The formulation is filtered (0.2 µm), then filled into cleaned containers and packaged for sterile workflows, including double-bagging and gamma irradiation per manufacturer documentation.

The bottle is supplied as a fully assembled trigger-spray unit so operators are not opening packaging to attach spray heads at point-of-use—an often-overlooked contamination pathway when teams are moving fast during setup and changeovers.

IPA is widely used in controlled environments because it evaporates quickly and, when properly applied, can leave low residue on compatible surfaces. The practical performance difference is usually not the alcohol itself—it is how consistently the blend, filtration, packaging, and operator technique stay inside your defined process window.

Important operational note: 70% IPA is commonly used for cleaning and residue removal. If your process requires validated disinfection claims (and especially sporicidal performance), follow your site disinfectant program and validation—do not assume a cleaning alcohol replaces a validated disinfectant rotation.

• Sterile workflow packaging: solution is filtered, filled into cleaned containers, double-bagged, and gamma-irradiated per manufacturer documentation.
• Traceability: bottles are lot coded and labeled with an expiration date to support recordkeeping.
• Lot-level documentation support: manufacturer indicates certificates of compliance/analysis/irradiation are available for sterile lots via its certificate center workflow.
• Endotoxin / sterile-suite relevance: manufacturer literature indicates lot endotoxin testing and references a medical-device bacterial endotoxin guideline (verify applicability to your product and acceptance criteria).
• Country of origin: not stated on the SOSCleanroom product page or in the listed manufacturer PDFs for this SKU; treat COO as “not published” unless confirmed by labeling or manufacturer documentation.

The most common cleanroom mistake with alcohol solutions is not the choice of IPA—it is uncontrolled delivery. Overspray, misting over open work, and “spray-and-wipe” habits can create airborne droplets and re-deposition. Use TX3270 to reinforce discipline, not speed-run cleaning.

• Overspray over open work: misting across benches or into airflow can drive droplets and redeposit contaminants.
• Treating “cleaning alcohol” as a disinfectant program: relying on IPA where your SOP requires validated disinfectants (or sporicidal agents) creates compliance and microbial risk.
• Re-using the same wipe face: a wet wipe with captured soils becomes a transfer mechanism and leaves streaks or films.
• Ignoring expiration / lot control: missing lot number capture or using expired bottles creates audit and QA exposure.
• Storage drift: storing outside stated ambient range or near heat sources can increase leakage risk and create avoidable EHS nonconformances.

If your process is written around sterile 70% IPA in a trigger spray, the meaningful comparison points are usually packaging/sterility validation, lot documentation, and delivery control (stream/mist) rather than “does it contain IPA.”

• Decon Labs CiDehol ST (sterile 70% IPA trigger spray formats): commonly selected for sterile cleanroom programs where WFI-based formulations or specific documentation packages are required (confirm exact bottle format and certificates per SKU).
• Contec Sterile 70% IPA (trigger spray formats): a comparable sterile alcohol solution with controlled packaging and lot identification; verify shelf life, trigger handling method, and SAL documentation for your workflow.
• Generic “sterile IPA” private labels: may fit less stringent programs, but often vary in documentation discipline and packaging details—evaluate carefully if your audit posture depends on lot-level certificates and validated sterile entry.

• Cleanroom range (manufacturer-stated, sterile): suitable for ISO Class 3–8 workflows (and corresponding legacy Class 1–100,000 / EU Grade A–D references) as published in manufacturer literature.
• Compounding pharmacy relevance: manufacturer technical data sheet indicates alignment with USP <797> and USP <800> requirements; validate against your facility program and documentation needs.
• Receiving/QA cues: verify double-bag integrity, lot number, expiration date, and request/retain the CoA and irradiation/processing certificate if your quality system requires it.
• Shipping constraints: treat as a flammable liquid; plan procurement lead times accordingly because air/expedited options may be restricted.