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Hospira Bacteriostatic Water, USP 30mL

Bacteriostatic Water, USP is a sterile, non-pyrogenic pharmaceutical-grade aqueous solution manufactured by Hospira Inc., a Pfizer company operating under current Good Manufacturing Practice regulations. This preparation consists of Water for Injection, USP preserved with 0.9% (9 mg/mL) benzyl alcohol, which functions as a bacteriostatic antimicrobial agent inhibiting microbial growth in opened containers during laboratory use. The benzyl alcohol preservative permits aseptic withdrawal of aliquots from a single container across multiple experimental sessions while maintaining sterility between uses. This USP-grade water serves as a reconstitution solvent for lyophilized peptides, proteins, and other research compounds requiring sterile aqueous diluents in laboratory settings. Each production lot undergoes terminal steam sterilization and comprehensive quality testing to ensure compliance with United States Pharmacopeia monograph specifications.

Product Specifications:

  • Composition: Water for Injection, USP with 0.9% (9 mg/mL) Benzyl Alcohol, NF (bacteriostatic preservative)
  • Volume: 30mL per sterile vial
  • Container Type: Type I borosilicate glass vial with sterile rubber closure and aluminum overseal
  • pH: 4.5 – 7.0 (per USP monograph)
  • Osmolality: Hypotonic (approximately 0 mOsm/kg)
  • Sterility Assurance Level: 10⁻⁶ (terminal steam sterilization)
  • Bacterial Endotoxin: <0.5 EU/mL per USP <85> Bacterial Endotoxins Test
  • Particulate Matter: Complies with USP <788> Particulate Matter specifications

FOR RESEARCH USE ONLY. NOT FOR HUMAN OR VETERINARY USE.

Strength

30mL

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SKU: PBL-HOSPIRA-BAC-WATER-VAR
Hospira BAC Water 30mL

Hospira BAC Water 30mL

$22.99

Pharmaceutical-grade sterile water containing 0.9% benzyl alcohol as bacteriostatic preservative. Used for reconstituting lyophilized peptides in laboratory settings. Multiple-dose 30mL vials maintain sterility for research applications. For research use only. Not intended for human or animal therapeutic use.

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Testing & Quality Assurance

Trust starts with transparency. Premier Bio Labs subjects every batch to comprehensive third-party testing before release, ensuring the materials powering your research meet pharmaceutical-grade standards.

Complete Batch Testing

Each product includes a Certificate of Analysis (COA) with verifiable data from independent laboratories.

COA Testing Parameters

  • Identity Verification – HPLC and Mass Spectrometry confirm molecular structure
  • Purity Analysis – HPLC quantification, typically ≥98%
  • Concentration Accuracy – Verified dosing levels
  • Molecular Weight – Mass spectrometry confirmation
  • Endotoxin Screening – LAL assay, <1.0 EU/mg
  • pH Testing – Solution stability validation
  • Sterility – Microbial contamination screening
  • Heavy Metals – Lead, mercury, cadmium analysis
  • Residual Solvents – Organic solvent detection
  • Moisture Content – Karl Fischer titration
  • Physical Inspection – Color, clarity, appearance
  • Traceability – Batch numbers, test dates, storage specs

All COAs include methodology, acceptance criteria, actual results, and QC team verification.

Legal Disclaimer:

The products offered by Premier Bio Labs are intended strictly for laboratory research purposes only and are sold exclusively to qualified professionals, institutions, and entities. These products are not for human consumption, veterinary use, or any application involving living organisms, including but not limited to diagnostic, therapeutic, or recreational purposes.
 

Prohibited Uses:

These products are not to be used as active pharmaceutical ingredients (APIs)for compounding or manufacturing drugs for human or veterinary use. It is strictly prohibited to administer these products to humans or animals under any circumstances. Premier Bio Labs does not condone, endorse, or permit the use of its products for the development, testing, or production of controlled substances or illegal compounds.

Regulatory Compliance:

Premier Bio Labs makes no claims, representations, or warranties that its products are approved by the U.S. Food and Drug Administration (FDA) or any other regulatory agency for any specific purpose. The statements regarding these products have not been evaluated by the FDA. These products are not intended to diagnose, treat, cure, or prevent any disease.
 

Liability Statement:

The purchaser assumes full responsibility for the safe handling, storage, transport, and use of any product obtained from Premier Bio Labs. Under no circumstances shall Premier Bio Labs, its owners, employees, or affiliates be held liable for any damages, injuries, or losses — direct or indirect — resulting from misuse, mishandling, or unauthorized application of its products.
 
Premier Bio Labs reserves the right to refuse sales to any individual or entity suspected of misuse, illegal activity, or non-compliance with these terms.
If you are uncertain about the safe and lawful use of these products, consult a qualified professional with expertise in laboratory research before purchase or use.
 
By completing a purchase with Premier Bio Labs, you acknowledge that you have read, understood, and agreed to this disclaimer in full.

Hospira Bacteriostatic Water, USP 30mL

Bacteriostatic Water, USP is a sterile, non-pyrogenic pharmaceutical-grade aqueous solution manufactured by Hospira Inc., a Pfizer company operating under current Good Manufacturing Practice regulations. This preparation consists of Water for Injection, USP preserved with 0.9% (9 mg/mL) benzyl alcohol, which functions as a bacteriostatic antimicrobial agent inhibiting microbial growth in opened containers during laboratory use. The benzyl alcohol preservative permits aseptic withdrawal of aliquots from a single container across multiple experimental sessions while maintaining sterility between uses. This USP-grade water serves as a reconstitution solvent for lyophilized peptides, proteins, and other research compounds requiring sterile aqueous diluents in laboratory settings. Each production lot undergoes terminal steam sterilization and comprehensive quality testing to ensure compliance with United States Pharmacopeia monograph specifications.

Product Specifications:

  • Composition: Water for Injection, USP with 0.9% (9 mg/mL) Benzyl Alcohol, NF (bacteriostatic preservative)
  • Volume: 30mL per sterile vial
  • Container Type: Type I borosilicate glass vial with sterile rubber closure and aluminum overseal
  • pH: 4.5 – 7.0 (per USP monograph)
  • Osmolality: Hypotonic (approximately 0 mOsm/kg)
  • Sterility Assurance Level: 10⁻⁶ (terminal steam sterilization)
  • Bacterial Endotoxin: <0.5 EU/mL per USP <85> Bacterial Endotoxins Test
  • Particulate Matter: Complies with USP <788> Particulate Matter specifications

FOR RESEARCH USE ONLY. NOT FOR HUMAN OR VETERINARY USE.

Strength

30mL

Reviews

There are no reviews yet.

Only logged in customers who have purchased this product may leave a review.

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