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TX650 TexQ Sterile Disinfectant Ready-to-Use 22 oz. Trigger Spray

Texwipe TX650 TexQ Sterile Disinfectant Ready-to-Use 22 oz. Trigger Spray

$202.35
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SKU:
TX650
Availability:
Stock Item
Shipping:
Calculated at Checkout
Quantity Option (Case):
12 Bottles Per Case (22 Fluid Ounce Trigger Spray Bottles)
Solution Type:
Quaternary Ammonium
Sterile:
Yes

Texwipe TX650 TexQ® Sterile Disinfectant (Ready-to-Use) — 22 oz Trigger Spray (12/Case)

Texwipe TX650 TexQ® is a ready-to-use, sterile, gamma-irradiated quaternary ammonium (quat) one-step cleaner/disinfectant in a fully assembled 22 oz trigger spray bottle. It is positioned for routine controlled-environment disinfection where repeatable application, broad-spectrum efficacy, and lot-level documentation matter. TexQ is 0.2 µm filtered, dye free, fragrance free, and designed to support daily use within a disinfectant rotation program (per your site SOP and required wet-contact time on the EPA label).

Program note: SOSCleanroom lists TexQ as gamma irradiated at no additional cost. Each bottle includes a functional-use label intended to support documentation (for example, date opened and operator initials) to reinforce day-to-day compliance.

Specifications:
  • Part number: TX650
  • Solution type: Quaternary Ammonium (Quat) disinfectant / cleaner (ready-to-use)
  • Sterile: Yes (gamma irradiated; sterile validated per manufacturer guidance)
  • Filtration: 0.2 µm filtered
  • Container: 22 oz trigger spray bottle (fully assembled)
  • Case pack: 12 bottles per case
  • EPA registration: EPA Reg. No. 10324-85
  • Active ingredients (per SDS): Quaternary ammonium compounds, benzyl-C12-16-alkyldimethyl, chlorides (≤0.3%); Dimethyldioctylammonium chloride (≤0.1%)
  • Performance positioning: Broad-spectrum bacteria/virus/fungi claims (multiple kill claims; contact time varies by organism — follow EPA label)
  • pH / odor profile (positioning): Neutral pH; free of dyes and fragrance
  • Shelf life (manufacturer guidance): 2 years (expiration date shown on label), including after opening/spraying
  • Transport note (per SDS): Not regulated as dangerous goods for DOT / IMDG / IATA
  • Sales restriction: For sale only in the United States
About the Manufacturer: 

TX650 is produced by ITW Texwipe, a long-established contamination-control manufacturer known for documentation discipline and process consistency across controlled-environment consumables. In the TexQ platform, the manufacturer emphasizes repeatable execution: an EPA-registered one-step formulation, 0.2 µm filtration, sterile validation and gamma irradiation for sterile-use programs, and packaging/labeling intended to support traceable, auditable cleaning and disinfection workflows.

 

From a program standpoint, TX650 is commonly staged for benches, carts, pass-through prep, and hard-surface disinfection where the team needs a ready-to-use, no-mix solution with a consistent application method (stream/coarse spray delivery, per the sprayer design) and an on-bottle documentation cue. Pair with compatible low-linting cleanroom wipers (no wiper is truly ‘zero-lint’ in every process condition) and straight-line wipe patterns to reduce re-deposition.

TX650 Features:
  • One-step cleaner/disinfectant: Cleans and disinfects in a single step to reduce labor and simplify SOP execution.
  • Gamma irradiated / sterile validated: Designed for sterile-use programs that require sterile packaged disinfectants.
  • Broad-spectrum claim set: Positioned with extensive kill claims against common bacteria, viruses, and fungi (follow EPA label for required contact time).
  • Mold/mildew control positioning: Includes an Aspergillus niger kill claim (per manufacturer literature/label claim set).
  • Dye free / fragrance free: Designed to avoid added dyes/fragrances and associated odor concerns.
  • Functional-use label: Intended to support documentation such as date opened and operator initials.
  • Neutral pH positioning: Designed to be less aggressive on many hard surfaces (always verify compatibility).
TX650 Benefits:
  • Repeatable disinfection: Ready-to-use sterile format reduces variability associated with mixing/dilution and supports consistent operator execution.
  • Audit-friendly documentation: Lot traceability plus on-bottle documentation cues help support cleanroom logs, deviations review, and routine inspections.
  • Workflow efficiency: A trigger-spray delivery format supports quick wetting of wipes and targeted application on equipment, carts, fixtures, and surfaces.
  • Rotation-program fit: Quat chemistry is commonly used as a routine disinfectant step in rotation with other chemistries (per your contamination-control strategy).
Common Applications:
  • Hard, non-porous surface disinfection in controlled environments
  • Equipment, carts, racks, shelves, and work-surface wipe-downs
  • Glass, stainless steel, plastic, vinyl upholstery, Plexiglas®, windows, and polycarbonate (verify compatibility and site SOP)
  • Commonly referenced in biotechnology, hospitals, medical device manufacturing, pharmaceutical manufacturing, and pharmacy environments
Best-Practice Use:
  • Pre-clean when needed: If visible soil or residues are present, pre-clean per SOP so the disinfectant can contact the surface effectively.
  • Control overspray: For critical work areas, apply TexQ to a compatible low-linting cleanroom wiper first, then wipe the surface to reduce airborne droplets.
  • Wet-contact time: Keep the surface visibly wet for the required EPA label contact time (varies by organism; many claims are 5–10 minutes, with select claims shorter — verify on label/TDS).
  • Straight-line wipe technique: Use overlapping straight strokes; rotate to a fresh wipe face frequently to avoid re-depositing contamination.
  • Documentation discipline: Use the bottle label fields (as applicable) and your log sheets for date opened, operator initials, and area/equipment identifiers.
  • Surface compatibility: Confirm compatibility with plastics, coatings, elastomers, adhesives, and sensitive finishes before broad deployment.

SOP disclaimer: The guidance above is a general best-practice template and must be adapted to your facility requirements, risk assessment, and validated cleaning/disinfection SOPs. Always follow the current Texwipe label instructions and SDS for safe handling, PPE, contact time, and disposal.

Selection Notes (This Sterile TexQ RTU Trigger Spray vs. Other Options)
  • Sterile vs. non-sterile disinfectants: Select sterile when your program requires sterile packaging/irradiation validation and controlled entry; use non-sterile formats where allowed by SOP and risk assessment.
  • Trigger spray vs. bulk formats: Trigger spray supports point-of-use control and repeatability; gallon formats can reduce change-outs for higher-volume areas.
  • Quat in a rotation: Quat disinfectants are often deployed for routine disinfection and paired with periodic sporicidal steps depending on your contamination-control strategy.
  • Documentation requirements: If your audits require lot traceability, expiration tracking, and “date opened” controls, TX650’s labeling/documentation ecosystem is a strong fit.
Other Similar Products Available From SOSCleanroom.com

TexQ Disinfectants

  • TX652: TexQ® Sterile Disinfectant Ready-to-Use (RTU), 1 gallon bottle, 4 bottles/case
  • TX651: TexQ Concentrate, 1 gallon concentrate, 4 bottles/case (confirm current availability/discontinuation status on the product page)

Notes: Building or tightening a disinfectant rotation, contact-time discipline, and wipe technique training? SOSCleanroom can help you align the right disinfectants and low-linting wipers to your surface set, residue profile, and audit expectations—with dependable supply and responsive support that understands real cleanroom workflows.

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

© 2026 SOS Supply. All rights reserved.

The Technical Vault Sterile Quat Disinfectant · EPA-Registered Claims · Contact-Time Discipline · ISO/USP/Annex 1 Mindset

Texwipe TX650 TexQ® Sterile Disinfectant (Ready-to-Use) — 22 oz Trigger Spray (12/Case)

Texwipe TX650 TexQ® is a ready-to-use, sterile, gamma-irradiated quaternary ammonium (quat) one-step cleaner/disinfectant supplied in a fully assembled 22 oz trigger-spray bottle. It is positioned for routine controlled-environment disinfection where repeatable application, documented execution, and EPA label compliance (wet-contact time by organism) are required.

At-a-glance (published attributes)
  • Part number: TX650
  • Solution type: Quaternary Ammonium (Quat) disinfectant / cleaner (ready-to-use)
  • Sterile: Yes (gamma irradiated; sterile validated per manufacturer guidance)
  • Filtration: 0.2 µm filtered
  • Format: Fully assembled 22 oz trigger spray bottle
  • Case pack: 12 bottles per case
  • EPA registration: EPA Reg. No. 10324-85
  • Fragrance / dye: Fragrance free; dye free
  • Active ingredients (per SDS excerpt on product page): Quaternary ammonium compounds, benzyl-C12-16-alkyldimethyl, chlorides (≤0.3%); Dimethyldioctylammonium chloride (≤0.1%)
  • Shelf life (manufacturer guidance on product page): 2 years (expiration date shown on label), including after opening/spraying
  • Sales restriction: For sale only in the United States

1) Where TX650 fits in a contamination control strategy

Quat disinfectants are commonly used as a routine disinfectant step for hard, non-porous surfaces (equipment exteriors, worktables, carts, racks, shelving, and touch points). TX650’s ready-to-use sterile format is typically selected to reduce variability associated with dilution/mixing and to support controlled-environment handling where sterile packaged disinfectants are required by SOP.

Important scope note (accuracy-first)

A quat disinfectant is not automatically a sporicide. Many validated programs use quat chemistry for routine disinfection and add a separate sporicidal step on a defined schedule based on risk assessment and facility CCS/SOPs.

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

In regulated cleanrooms, compliance is built on validated procedures, trained behavior, and documentation control. USP <797> and USP <800> expect cleaning/disinfection activities to be governed by SOPs (agent selection, technique, frequencies, PPE), and EU GMP Annex 1 emphasizes a contamination control strategy (CCS), validated disinfection processes, and disciplined operator practices. ISO cleanroom operations guidance similarly supports an operations control program covering personnel practices, cleaning, and material movement.

Key compliance reality: standards do not “approve” a specific disinfectant brand. Facilities must select, qualify, and document disinfectants and then execute exactly as validated (including dwell time and wipe technique).

3) What actually drives performance (EPA label discipline)

Disinfectants most often “fail” operationally due to missed wet-contact time, poor wiping technique (re-deposition), and weak documentation across shifts. TX650 is positioned to reduce those variables with a ready-to-use format and a functional-use label concept (e.g., open date/initials) as part of a documentation-driven program.

Best-practice use (audit-resilient technique)
  • Confirm dwell time on the current EPA label/TDS: contact time varies by organism—your SOP must match the label.
  • Spray-to-wipe for control: in sensitive zones, wet a sterile wiper (damp, not dripping) and wipe to reduce overspray/aerosolization.
  • One direction + overlap: straight strokes with overlap; rotate to a fresh wipe face often to prevent re-depositing soils.
  • Keep the surface visibly wet: if it dries early, re-apply per your SOP to maintain the validated wet-contact condition.
  • Follow with sterile 70% IPA when required: many programs use IPA as a “finish” step to manage residues and standardize surface state (per SOP).

4) Donning discipline & PPE interface control

In critical environments, deviations commonly trace to touch events and interface gaps (adjusting eyewear/hoods, contacting non-controlled objects, poor glove–sleeve overlap). Ensure personnel are fully gowned before introducing disinfectants into ISO-classified areas, and define glove sanitization, re-entry, and “touch-event” recovery steps in SOPs.

5) System pairings (repeatable wipe-down discipline)

TX650 is typically paired with sterile, low-linting cleanroom wipers and a validated PPE system. Final selection must match your ISO class, surface set, residue limits, and SOP validation.

6) Selection notes (why teams standardize TexQ RTU)

  • Reduces dilution risk: ready-to-use chemistry supports consistent execution versus in-house dilution practices.
  • Supports documentation discipline: lot traceability plus functional-use labeling concepts help standardize shift-to-shift control.
  • Rotation-program fit: quat chemistry is commonly used as the routine disinfectant step within broader rotation strategies (per CCS/SOP).
  • Controlled-environment handling: sterile, gamma-irradiated positioning supports aseptic programs requiring sterile-packaged disinfectants.

7) Surface compatibility (validate — don’t assume)

Even “mild” disinfectants can interact with certain labels, inks, adhesives, coatings, and plastics. Treat compatibility as a qualification activity: test on representative materials, define acceptance criteria, and document outcomes in SOPs before broad deployment.

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. Disinfectant selection, EPA label compliance, required wet-contact time, application technique, residue controls, rotation strategy, PPE requirements, 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 label/TDS/SDS.

© 2026 SOS Supply. All rights reserved.