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Bacteriostatic Water is a sterile, preservative-containing diluent formulated with 0.9% benzyl alcohol. It is commonly utilized for the reconstitution and dilution of lyophilized research compounds and peptides in laboratory settings.
Independent analytical testing performed on supported batches.
Documentation linked to production and verification records.
Verification resources available for supported products and batches.
Synonym: Bacteriostatic Water for Injection
CAS Number: 7732-18-5 (Water)
Composition: Sterile Water for Injection containing 0.9% Benzyl Alcohol as a preservative
Format: Multi-dose sterile diluent solution
Bacteriostatic Water is a sterile, non-pyrogenic aqueous solution commonly utilized as a diluent for the reconstitution of lyophilized compounds in laboratory and research settings. The solution contains 0.9% benzyl alcohol, which acts as a preservative to inhibit the growth of microorganisms following initial puncture of the vial.
Its preservative content distinguishes it from Sterile Water for Injection, allowing for multiple withdrawals under appropriate handling conditions.
Bacteriostatic Water serves as a reconstitution and dilution medium rather than an active research compound.
Key characteristics include:
The solution itself possesses no pharmacological activity beyond its role as a preservative-containing vehicle.
Bacteriostatic Water consists of:
Key features include:
Bacteriostatic Water is commonly utilized for:
It serves as a standard diluent for numerous peptide and biochemical research applications.
This product is intended for laboratory research use only and is not approved for human or veterinary applications.
Every batch undergoes independent third-party analytical testing for purity, identity, and consistency. Relevant documentation is maintained to support verification and traceability.
Yes. Analytical documentation is maintained for supported products and batches. Verification resources are available to help researchers review relevant testing information.
Each production batch is assigned documentation that links materials to associated testing records and verification resources, helping maintain consistency and transparency.
Yes. Analytical documentation is maintained for supported products and batches. Verification resources are available to help researchers review relevant testing information.
Each production batch is assigned documentation that links materials to associated testing records and verification resources, helping maintain consistency and transparency.
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