Lot #2657261

$12.00

Pharmaceutical-Grade Peptide Reconstitution Solvent

RECONSTITUTION SOLUTION [10ml]

10ml / vial

Bacteriostatic water

≥99% HPLC

4.9 / 5

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Stock up. Stable for 24 months lyophilized at −20°C.
$12.00
1 bottle · RECONSTITUTION SOLUTION [10ml]

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≥99% HPLC Purity

Made in the USA

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Compound Profile

Bacteriostatic Water for Injection (BWFI)

Bacteriostatic Water for Injection (BWFI) is a sterile, non-pyrogenic aqueous preparation containing 0.9% benzyl alcohol (9 mg/mL) as a bacteriostatic preservative, prepared in accordance with United States Pharmacopeia (USP) standards. The 0.9% benzyl alcohol concentration inhibits microbial growth, enabling multi-dose use of reconstituted research solutions when stored under appropriate conditions. BWFI is the standard diluent for reconstituting lyophilized peptide research compounds prior to experimental use. Each vial is sterility-tested and endotoxin-screened.

— Component 01
Bacteriostatic Water · 10ml
Class
Sterile bacteriostatic water for injection (BWFI)
Sequence
Non-peptide pharmaceutical solvent — 0.9% benzyl alcohol in sterile water
CAS Number
7732-18-5 (water) / 100-51-6 (benzyl alcohol)
Molecular Formula
H₂O / C₇H₈O
Molecular Weight
18.02 / 108.14 g/mol
Per-component purity
USP Grade
Form
Sterile aqueous solution, multi-dose vial
Identity (LC-MS)
All confirmed
Sterility / LAL
PASS
Storage
15-25°C (room temp), sealed, dry
Origin
Made in the USA
In the Literature

Reconstitution Reference

Bacteriostatic Water for Injection (BWFI) is a pharmaceutical-grade solvent standardized under USP and screened for sterility per USP and endotoxin per USP . The 0.9% benzyl alcohol preservative provides antimicrobial protection through membrane disruption of microbial cells. For peptide reconstitution research, BWFI is preferred over plain sterile water because it extends the usable life of reconstituted solutions when stored refrigerated (2-8°C) and used within 28 days. Research compounds should be reconstituted by injecting BWFI along the vial wall, gently swirling (never vortexing), and allowing complete dissolution before use.

For research use only. Statements above describe published research literature and do not constitute health, medical, or therapeutic claims for either compound or for the blend. Not for human or veterinary use. Not evaluated by the FDA.

Documented Research Areas

  • Bacteriostatic preservation via 0.9% benzyl alcohol (w/v) per USP specification
  • Sterility tested per USP <71> — membrane filtration and direct inoculation methods
  • Endotoxin burden tested via LAL assay per USP <85>
  • Compatible with lyophilized peptide solubility and stability profiles
  • Multi-dose septum vial rated for repeated needle access without coring
  • pH 4.5–7.0 compatible with standard 1ml insulin syringe reconstitution protocols

Selected Studies · Peer-Reviewed Literature

A curated list of published peer-reviewed papers indexed in PubMed where BPC-157 has been studied. Provided for research-context only. Linking to the literature does not constitute endorsement of any therapeutic application.

Compound database reference for chemical and structural data:

Transparency

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Each batch ships with a third-party Certificate of Analysis from BioRegen Analytical. HPLC purity, mass-spectrometry identity, sterility, and LAL endotoxin screening. Every test, every lot.

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Certificate of Analysis

ProductBacteriostatic Water for Injection (BWFI)
Preservative0.9% Benzyl Alcohol (w/v) · CAS 100-51-6
SolventSterile Water for Injection · CAS 7732-18-5
Volume10ml / vial
pH4.5–7.0
Sterility (USP <71>)PASS
Endotoxin (LAL)PASS
Date TestedOn file

Pairs With

Related compounds.

Other research peptides in the Elixser catalog cited alongside the BPC-157 + TB-500 blend in the published research literature.

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