Advanced Acidic Phenolic Cleanroom Disinfectants (LpH)

Advanced Acidic Phenolic Cleanroom Disinfectants (LpH)

Advanced Acidic Phenolic Cleanroom Disinfectants

Optimize your contamination control program with our broad-spectrum acidic phenolic disinfectants. Engineered specifically for high-traffic pharmaceutical manufacturing and aseptic environments, these formulations provide highly effective, routine cleaning for hard, non-porous surfaces. With a rapid 10-minute contact kill time, they significantly reduce facility downtime while ensuring uncompromising environmental protection against common bacteria, viruses, and fungi.

Tailored Formats for Every Cleanroom Grade

We supply a versatile portfolio of phenolic disinfectants engineered to meet your facility's exact standard operating procedures:

  • Standard Concentrates: Powerful, cost-effective formulations ideal for routine disinfection in general controlled environments.
  • Sterile Formats: Gamma-irradiated and cleanroom double-bagged for simplified, secure introduction directly into strict aseptic processing areas.
  • Premeasured WFI Solutions: The ultimate in compliance and convenience. Features perfectly calibrated disinfectant pouches paired with 0.2-micron filtered USP Water for Injection (WFI), eliminating mixing errors on the facility floor.

 

Key Product Benefits & Compliance:

  • Proven Broad-Spectrum Efficacy: Highly effective against a wide range of pathogens, including tuberculosis, at a standard 0.8% v/v (1:128) dilution rate.
  • Ideal for Rotational Programs: Designed for flexible application (manual wiping or spraying), making them the perfect acidic component to rotate with alkaline disinfectants or sporicides to prevent microbial resistance.
  • Minimized Environmental Impact: Formulated with advanced biodegradable surfactants, delivering robust cleaning power while significantly reducing environmental impact upon disposal.
  • Complete Quality Assurance: Every batch includes complete lot traceability and is fully documented by a Certificate of Analysis (CoA) to seamlessly support your facility's validation protocols.

Talk to an Industry Specialist

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