Sterile, ready-to-use 70% denatured ethanol (EtOH) solution is ideal for cleanroom use. Solution is filtered to 0.2 µm to remove particulate contamination. It evaporates completely, leaving no residue.
Solution is filtered to 0.2 µm to remove particulate contamination
- Evaporates completely, leaving no residue
- Bottled and double-bagged within an ISO 5 cleanroom
- Gamma-irradiated to a sterility assurance level (SAL) of 10⁻⁶
Made according to USP specifications and packaged in a cleanroom. Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits and each lot also undergoes a USP 14-day sterility test. Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits.
: Each lot is tested for sterility via the USP 14-day sterility test and for bacterial endotoxins prior to release. A QR code can be found on each case of Sanihol® ST which is linked to a copy of the lot specific document which details QC, irradiation, sterility, and bacterial endotoxin limits. All lots of Sanihol® ST are guaranteed to contain less than 0.25 EU/ml, the endotoxin level criterion for WFI.
: Each container is double-bagged and gamma-irradiated to ensure sterility.
Sterile, ready-to-use 70% denatured ethanol (EtOH) solution is ideal for cleanroom use. Solution is filtered to 0.2 µm to remove particulate contamination. It evaporates completely, leaving no residue.
Solution is filtered to 0.2 µm to remove particulate contamination
- Evaporates completely, leaving no residue
- Bottled and double-bagged within an ISO 5 cleanroom
- Gamma-irradiated to a sterility assurance level (SAL) of 10⁻⁶
Made according to USP specifications and packaged in a cleanroom. Each lot undergoes a bacterial endotoxin test to ensure that the product meets or exceeds Water-for-Injection quality in endotoxin limits and each lot also undergoes a USP 14-day sterility test. Each case is shipped with lot specific documentation which details QC, irradiation, sterility, and bacterial endotoxin limits.
: Each lot is tested for sterility via the USP 14-day sterility test and for bacterial endotoxins prior to release. A QR code can be found on each case of Sanihol® ST which is linked to a copy of the lot specific document which details QC, irradiation, sterility, and bacterial endotoxin limits. All lots of Sanihol® ST are guaranteed to contain less than 0.25 EU/ml, the endotoxin level criterion for WFI.
: Each container is double-bagged and gamma-irradiated to ensure sterility.