Bacteriostatic Water

For research use only — not for human or veterinary use.

Analytical Verification (COA)

Each batch of Bacteriostatic Water supplied by Grail Formula undergoes independent third-party laboratory verification to confirm formulation accuracy, chemical composition and microbiological safety.

Analytical testing for this batch was performed by Liquilabs s.r.o. (Czechia) using validated analytical methods and laboratory testing protocols.

Batch: GF082025018

Key analytical results include:

• Benzyl Alcohol Content: 0.9090 percent
• pH Level: 6.83
• Bacterial Endotoxins: not detected

Independent laboratory testing confirms that the solution composition falls within validated analytical specifications and demonstrates no detectable endotoxin contamination.

These analytical procedures ensure traceability, composition verification and laboratory-grade formulation consistency.

Product Overview

Bacteriostatic Water is a sterile aqueous solution containing a small concentration of benzyl alcohol used as a preservative agent.

The presence of benzyl alcohol helps inhibit microbial growth in multi-use laboratory preparations and experimental compound reconstitution procedures.

This preparation is supplied in a sealed sterile vial designed for controlled laboratory environments. The formulation is intended for research applications requiring sterile solvent systems for compound dilution or reconstitution.

The defined chemical composition and laboratory verification make bacteriostatic water a commonly used solvent system in biochemical research and experimental laboratory protocols.

Compound Overview

Bacteriostatic water consists primarily of sterile water combined with a low concentration of benzyl alcohol as a bacteriostatic preservative.

In laboratory environments, bacteriostatic solutions are used to reduce the risk of microbial growth when preparing or storing reconstituted research compounds.

Benzyl alcohol acts as a preservative by inhibiting the growth of certain bacteria and microorganisms, thereby supporting stability during short-term laboratory use.

The controlled composition and sterile preparation allow the solution to be used in experimental protocols requiring high-purity solvent systems.

Historical Background and Scientific Context

Sterile water preparations have long been utilised in laboratory science and pharmaceutical research as a base solvent for compound preparation.

The addition of bacteriostatic preservatives such as benzyl alcohol became common practice during the twentieth century to allow multi-use solutions with reduced microbial contamination risk.

These preservative-containing solutions are widely referenced in research environments where sterile reconstitution of experimental compounds is required.

Modern laboratory-grade bacteriostatic water formulations are produced under strict analytical verification procedures to ensure composition accuracy and microbiological safety.

Mechanistic Focus in Research

Within laboratory environments, bacteriostatic water is commonly utilised as a sterile solvent system supporting experimental compound preparation.

Research protocols frequently involve the solution in laboratory procedures examining:

• Reconstitution of lyophilized research compounds
• Preparation of experimental peptide solutions
• Laboratory solvent system testing
• Biochemical dilution protocols
• Controlled laboratory formulation studies
• Experimental compound stability evaluation
• Preparation of in vitro testing solutions

These applications support laboratory research requiring sterile solvent systems and controlled experimental preparation conditions.

Research Applications

In controlled laboratory environments, bacteriostatic water may be utilised as a sterile solvent for preparation and dilution of experimental research compounds.

Examples of research applications include:

• Lyophilized compound reconstitution
• Peptide preparation protocols
• Experimental solvent systems
• Laboratory dilution procedures
• Biochemical solution preparation
• Controlled in vitro testing solutions
• Research compound formulation studies

Grail Formula Quality

Every Grail Formula research compound and laboratory preparation is produced under strict quality control procedures designed to support reliable laboratory experimentation.

Each batch undergoes independent analytical testing to verify:

• Composition accuracy
• Chemical identity
• Formulation verification
• Microbial safety
• Endotoxin levels
• Batch traceability

All testing is performed by independent laboratories to ensure transparent verification and reproducible research material.

Research Use Limitation

• Used solely for laboratory research
• Not permitted for clinical trials involving humans
• Not permitted for human or veterinary administration
• Not permitted for investigational human use

Independently verified by Liquilabs s.r.o. (Czechia)
Benzyl alcohol content 0.9090 percent
pH value 6.83 within validated range
Bacterial endotoxin not detected (USP )
Validated chromogenic LAL assay testing
Batch GF082025018
For research use only — not for human or veterinary use

For laboratory research only. Not intended for human consumption, injection, or cosmetic use.

This product is for research purposes only. Not for human use or diagnostic/therapeutic applications. Keep out of reach of children.