High - Tech Conversions HBG703016797, Virtu - Clean Sterile 70% IPA, Case of 12 MTESolutions

High-Tech Conversions HBG703016797, Virtu-Clean Sterile 70% IPA, Case of 12

High-Tech Conversions SKU: HBG703016797
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High-Tech Conversions HBG703016797 Virtu-Clean Sterile 70% IPA Trigger Spray, 16 oz, Case of 12

Virtu-Clean™ HBG703016797 is a sterile 70% isopropyl alcohol / 30% purified water solution in a 16 oz trigger spray bottle, gamma-irradiated to a sterility assurance level (SAL) of 10⁻⁶, filtered at 0.1 microns — finer than the industry-standard 0.22 micron filtration — for use in ISO Class 5 and higher cleanrooms, compounding pharmacies, and pharmaceutical manufacturing environments. The 0.1 micron filtration removes a broader range of particulates and microbial contamination than standard 0.22 micron-filtered IPA, providing an additional layer of cleanliness assurance for critical surface disinfection applications. Pyrogen free and spot-free drying — no residue on cleaned surfaces. USP <797> and USP <800> compliant; sterile 70% IPA is referenced throughout USP <797> and <800> requirements as appropriate for a wide variety of compounding processes and procedures. Double-bagged for cleanroom introduction. Applications include wiping down gloved hands, vials, equipment, supplies, countertops, floors, and walls. Sold in cases of 12 bottles.

Sold in cases of 12 bottles (16 oz trigger spray bottle each).

Specifications

SKU HBG703016797
Brand High-Tech Conversions
Product Line Virtu-Clean™
Solution 70% isopropyl alcohol (IPA) / 30% purified water
Container 16 oz trigger spray bottle
Filtration 0.1 micron (exceeds industry standard 0.22 micron)
Sterility Gamma-irradiated, SAL 10⁻⁶
Pyrogen Free Yes
Residue Spot-free drying, no residue
Packaging Double-bagged, 12 bottles/case
Cleanroom Compatibility ISO Class 5 and higher
Regulatory Compliance USP <797> and USP <800> compliant
Application Surface disinfection, gloved hand wiping, vial and equipment cleaning, countertops, floors, walls in ISO Class 5+ cleanrooms and compounding pharmacies
Industries Pharmaceutical/biologics, compounding pharmacies, medical device, semiconductor, laboratories

Frequently Asked Questions

Why is 0.1 micron filtration better than the standard 0.22 micron for sterile IPA?

Filtration at 0.1 microns removes a broader range of particulates and microbial contamination than the industry-standard 0.22 micron filtration. While 0.22 micron filtration is the minimum required for sterile filtration per USP standards, 0.1 micron filtration provides an additional margin of cleanliness assurance — particularly important in ISO Class 5 aseptic processing environments and Grade A/B cleanrooms where the highest possible IPA purity is required for validated surface disinfection protocols.

What does gamma-irradiated to SAL 10⁻⁶ mean?

SAL 10⁻⁶ means there is no more than a 1-in-1,000,000 probability that a single viable microorganism remains in the product after sterilization. Gamma irradiation is a validated terminal sterilization method widely accepted in pharmaceutical manufacturing. This sterility assurance level meets the requirements for sterile IPA used in aseptic processing areas, Grade A/B cleanrooms, and USP <797>/<800> compounding environments.

Why is Virtu-Clean double-bagged?

Double-bagging allows the product to be introduced into ISO Class 5 and higher cleanrooms using standard bag-in/bag-out transfer procedures — the outer bag is wiped down and removed in the lower-classification anteroom, and the inner bag is wiped down before the product enters the critical zone. This prevents contamination from the external packaging from entering the cleanroom environment.

Is Virtu-Clean 70% IPA compliant with USP <797> and USP <800> requirements?

Yes — Virtu-Clean HBG703016797 is USP <797> and USP <800> compliant. Sterile 70% IPA is referenced throughout USP <797> and <800> requirements as appropriate for surface disinfection, gloved hand disinfection, and cleaning of equipment and supplies in sterile compounding environments. Always verify compliance with your facility’s specific SOPs and state board of pharmacy requirements.

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