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Cidehol St 70% 12X32Oz
CiDehol® ST Sterile 70% IPA with WFI, Decon Labs
Catalog #: CA89125-196
Supplier:  Decon Labs
Cidehol St 70% 12X32Oz
CiDehol® ST Sterile 70% IPA with WFI, Decon Labs
Catalog #: CA89125-196
Supplier:  Decon Labs
Restricted Products: To process your orders without delay, please provide the required business documentation to purchase this product.

To order chemicals, medical devices, or other restricted products please provide ID that includes your business name & shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of ID are:

  • • State issued document with your organization's Federal Tax ID Number
  • • State issued document with your organization's Resale Tax ID Number
  • • City or County issued Business License
  • • State Department of Health Services License
  • • Any other ID issued by the State that includes the business name & address

* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. VWR will not lift restrictions for residential shipping addresses.

Specifications

  • Description:
    Trigger Spray Bottle
  • Size:
    946 mL (32 oz.)
  • Supplier No.:
    8332F

Specifications

About this item

Sterile, ready-to-use 70% isopropyl alcohol (IPA) solution made with WFI is ideal for cleanroom use

Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) 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.

Sterile, ready-to-use 70% isopropyl alcohol (IPA) solution made with WFI is ideal for cleanroom use

Solution is filtered to 0.2µm to remove particulate contamintion. It evaporates completely, with no rinsing required. Made according to USP specifications and packaged in an ISO Class 5 (FED-STD-209E Class 100/M3.5) 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.

Ordering information: Each lot is double-bagged and gamma-irradiated to ensure sterility.
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