High-Purity Cleanroom Alcohol Solutions (Septihol)

High-Purity Cleanroom Alcohol Solutions (Septihol)

Ensure optimal surface cleanliness and rapid residue removal with our premium, ready-to-use cleanroom alcohol solutions. Formulated with USP 70% reagent-grade alcohol (Isopropyl or Ethyl) and 30% USP Purified Water, these solutions are designed for frequent, effective use on critical production surfaces, equipment, and gloved hands. Engineered entirely without stabilizers or denaturants, our alcohols provide a rapid evaporation rate that minimizes facility downtime while completely preventing particulate or chemical residue left behind.

Tailored Formats for Strict Aseptic Compliance

We supply cleanroom alcohol in formats specifically designed to seamlessly integrate into your standard operating procedures while eliminating the risk of in-house dilution errors:

  • Standard Ready-To-Use (RTU): Pre-mixed and 0.22-micron filtered for immediate, effective cleaning in general controlled environments.
  • Sterile WFI Solutions: The ultimate standard for Grade A/B aseptic areas. Blended with high-quality USP Water for Injection (WFI), these solutions are double-bagged, gamma-irradiated, and rigorously sterility-tested prior to release.
  • Optimized Aerosol Delivery: Available in specialized bag-on-valve aerosol cans that enable maximum discharge and angled use, reducing waste and improving operator safety. Perfect for pairing with wall-mounted or portable stainless-steel dispensers.

Key Product Benefits & Quality Assurance:

  • Reliable Broad-Spectrum Performance: Demonstrated biocidal and fungicidal effectiveness (including EPA-registered formulations), making them the ideal component for your qualified microbial control program, even in the presence of organic soil.
  • Rapid Evaporation: Fast-acting formulas minimize downtime and dramatically reduce contamination risks during critical interventions.
  • Proven Quality Assurance: Every lot includes complete traceability and is documented by a Certificate of Analysis (CoA) to effortlessly support your facility’s stringent validation assistance protocols.

Talk to an Industry Specialist

Our team understands GMP environments, classification requirements, and what your QA team needs to stay audit-ready.

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