Cleanroom wipe-downs fail most often for simple reasons: inconsistent wetting, “mystery” spray bottles with unclear history, and gaps in lot documentation during audits or deviations. TX3273 is designed to reduce those variables. It is a sterile, ready-to-use 70% isopropanol (IPA) solution packaged in a fully assembled 32 fl oz trigger sprayer, double-bagged for controlled entry, with lot coding and an expiration date to support traceable use in critical areas.

• Routine surface cleaning and residue removal on compatible materials (benches, carts, pass-through staging, equipment exteriors).
• Wipe-down of items entering controlled environments (phones, notebooks, tools, secondary containers) where your program calls for sterile alcohol.
• Glove wipe steps in sterile suites when your SOP specifies sterile IPA as part of an aseptic workflow.
• Standardized wetting for cleanroom wipers (often used to achieve repeatable “spray-to-wipe-to-surface” coverage across shifts).

• Sterile, documented, and audit-friendly: gamma-irradiated sterile alcohol with lot traceability and an expiration date.
• Repeatable application: fully assembled trigger sprayer supports consistent wetting without ad-hoc decanting.
• Cleanroom-ready packaging: double-bagged packaging supports controlled entry and cleaner handling at the gowning boundary.
• Low-residue cleaning behavior: 70% IPA is widely selected for wipe-downs where fast evaporation and minimal residue are important (surface-dependent).
• Program continuity: SOSCleanroom’s long-standing relationship with ITW Texwipe supports steady supply and predictable documentation sets for receiving and QA review.

TX3273 is a 70% by volume USP-grade isopropanol (isopropyl alcohol) and 30% USP-purified water solution. The solution is submicron/0.2 µm filtered and filled into cleaned containers, then double-bagged and gamma-irradiated for sterility assurance.

The delivery format is a fully assembled 32 oz (946 mL) trigger spray bottle designed for controlled dispensing. Texwipe describes an adjustable, non-atomizing spray with stream delivery or coarse spray options. Texwipe also describes identification features such as 5 color indicator dots to support bottle segregation in multi-chemical environments.

The table below consolidates attributes that matter most for cleanroom receiving, SOP alignment, and day-to-day wipe-down consistency. If an attribute is not published for TX3273 in the source basis, it is shown as “not published.”

Attribute	TX3273
Part number	TX3273
Solution type	70% Isopropyl Alcohol (sterile)
Composition	70% by volume USP-grade isopropanol + 30% USP-purified water
Filtration	0.2 µm filtered (submicron)
Sterilization / sterility assurance	Gamma-irradiated; SAL 10-6
Bottle size / format	32 fl oz (946 mL) trigger spray bottle; fully assembled
Packaging	Double-bagged in solvent-safe packaging
Case pack	12 poly bottles per case
Traceability	Lot coded; expiration date marked; certificates (CoC/CoA/irradiation) referenced by manufacturer
Shelf life	Sterile: 2 years from date of manufacture
Storage conditions	Ambient storage defined as 59°F (15°C) to 86°F (30°C)
Shipping constraints	Ground shipping only (Consumer Commodity ORM-D / limited quantity handling per seller programs)
Country of origin	Not published in source basis for this SKU

In cleanrooms, “performance” for 70% IPA usually means: predictable evaporation, low residue, and reliable control of handling variability (who sprayed what, when, and with which bottle). TX3273 is positioned as a standardized, sterile, traceable alcohol format for those outcomes. It is commonly paired with low-linting cleanroom wipers when your process calls for a controlled wet wipe step.

Characteristic	What it means for use	Published basis (typical/statement)
Residue (NVR)	Helps reduce film risk on optics, stainless, and critical assemblies when surfaces are compatible and wiping is controlled.	Typical limit referenced: does not exceed 5 mg (0.01%) / 5 mg in 50 mL (TDS).
Sterility assurance	Supports sterile-area entry and documentation expectations where sterile alcohol is specified by SOP.	Gamma irradiated; SAL 10-6 (manufacturer TDS references AAMI guidance).
Endotoxin control	Relevant for medical device and aseptic workflows that track bioburden/endotoxin risk on handled surfaces.	Manufacturer sheet references endotoxin testing and an FDA guideline limit statement (medical device context).
Fill/pack environment	Reduces variability compared to in-house decanting, supporting more repeatable incoming quality and use consistency.	TDS states filled in an ISO Class 5 environment; double-bagged in solvent-safe bags.
SDS hazard profile	Drives EHS controls: ignition source control, ventilation, eye protection, and spill response discipline.	SDS classifies as highly flammable; eye irritation hazard; may cause drowsiness/dizziness (single exposure).

TX3273 is supplied as 12 poly bottles per case, each a fully assembled 32 oz trigger sprayer. Packaging is described as double-bagged for contamination control and controlled entry practices. The solution is described as 0.2 µm filtered and gamma-irradiated to a sterility assurance level of 10^-6.

For QA and receiving: each bottle is described as lot coded with an expiration date. Manufacturer documentation commonly references certificates of compliance and analysis, and (for sterile products) irradiation documentation.

Country of origin: not stated for TX3273 in the source basis listed below. If your program requires COO confirmation, treat it as a receiving requirement and request it as part of supplier documentation before qualification.

Cleaning vs. disinfection note: 70% IPA is widely used for cleaning and residue removal. For validated disinfection or sporicidal control, follow your site-approved disinfectant rotation, wet-contact times, and documentation requirements. Always reference the current SDS for handling, ventilation, ignition-source control, spill response, and disposal guidance.

• Overspray and aerosol risk in sensitive work: move to “spray-to-wipe” where needed.
• Cross-use bottle confusion: maintain segregation and labeling so “one bottle becomes one chemistry.”
• Dirty trigger/nozzle handling: treat the sprayer head as a critical contact point.
• Residue redeposition: rotate wipe faces and do not polish with a loaded wipe.
• Material incompatibility: qualify before broad rollout to avoid stress-cracking or coating haze.

Closest alternatives are typically other sterile 70% IPA trigger-spray programs in comparable bottle sizes and documentation depth. Compare sterility method, case pack, and certificate availability—not just concentration.

• Decon Labs CiDehol ST (sterile 70% IPA formats): validate bottle format and documentation for your SOP.
• Fisherbrand / house-brand sterile 70% IPA trigger sprays: confirm sterility documentation and traceability depth for audits.
• Other cleanroom alcohol programs (Avantor/VWR or specialty suppliers): compare packaging discipline and certificate availability.

TX3273 is typically selected for cleanrooms and controlled environments where sterile alcohol is part of a documented wipe-down process and where lot traceability is expected. It is a strong fit when your operation wants fewer variables: consistent bottle format, consistent packaging, and consistent supporting documentation. SOSCleanroom’s long-standing partnership with ITW Texwipe supports that reliability emphasis through continuity of supply and predictable documentation sets.