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èvelan Bio-Molecular Reference: Analytical-grade Bacteriostatic Water for Injection (USP) formulated with 0.9% (9 mg/mL) benzyl alcohol preservative. Designated as the standardized reconstitution solvent for laboratory research into lyophilized peptides, recombinant proteins, and enzymatic assays requiring repeated multi-dose septum penetration.

Chemical & Analytical Specifications

Solvent Identifier Bacteriostatic Water (BAC Water) Reagent Grade
Chemical Formula H2O + C7H8O (Benzyl Alcohol 0.9% w/v)
CAS Registry Numbers 7732-18-5 (Water) / 100-51-6 (Benzyl Alcohol)
pH & Osmolarity pH 4.5 – 7.0 | ~83 mOsmol/L (Non-pyrogenic, <0.25 EU/mL)
Vial Architecture Type I Borosilicate Glass with Chlorobutyl Rubber Septum
Research Classification In-Vitro Reconstitution & Analytical Storage Diluent

Laboratory Reconstitution & Handling Protocol

To maintain sterility and peptide integrity, swab the vial septum with sterile 70% isopropyl alcohol prior to needle insertion. Using a sterile luer-lock syringe (27G to 30G), slowly introduce the diluent into the lyophilized peptide vial by directing the liquid stream down the interior glass wall. Allow the lyophilized powder to dissolve naturally through gentle circular swirling; avoid vigorous shaking or vortexing to prevent protein denaturing. Sealed vials should be stored at room temperature (15°C to 30°C). Post-puncture solutions must be maintained at 2°C to 8°C and utilized within 28 days.

REGULATORY COMPLIANCE NOTICE All èvelan research products are strictly synthesized and supplied for laboratory research, analytical characterization, and scientific assay evaluation only. These materials are not intended, formulated, or approved for human, clinical, veterinary, or diagnostic application. Distribution is restricted to authorized personnel who affirm adherence to relevant institutional and laboratory safety protocols.

BAC Water (Bacteriostatic Water)

$220.36

Research Pathways & Profile

Bacteriostatic Water (BAC Water) supplies an analytical-grade, sterile non-pyrogenic reconstitution solvent formulated with 0.9% (9 mg/mL) benzyl alcohol USP. In biochemical and molecular research, it serves as the essential diluent for lyophilized peptides, proteins, and biochemical reagents. The benzyl alcohol bacteriostatic agent suppresses microbial and fungal proliferation across repeated vial access, allowing multi-dose laboratory aliquoting for up to 28 days under refrigerated conditions (2°C to 8°C) without compromising peptide solubility or bio-activity. Supplied strictly for laboratory research and analytical assay evaluation.

Format & Concentration: 3ml Vial
≥99% HPLC Analytical Standard
Synthesized in Certified Facility
Direct Express Lab Fulfillment
Analytical Specifications & Sequence

Solvent Formulation: Sterile Water for Injection (USP) containing 0.9% w/v Benzyl Alcohol (C7H8O, CAS: 100-51-6, Molecular Weight: 108.14 g/mol). Osmolarity: ~83 mOsmol/L. pH Range: 4.5 to 7.0. Pyrogenicity: Non-pyrogenic (<0.25 EU/mL endotoxin verified). Purity: USP Reagent Grade. Container Closure: Type I borosilicate glass vial with chlorobutyl elastomeric stopper and tamper-evident aluminum flip-off crimp seal.

Handling, Solvent & Storage Guidelines

Laboratory Reconstitution Protocol: Cleanse vial septum using a sterile 70% isopropyl alcohol prep pad prior to needle puncture. Use a sterile luer-lock syringe (27G to 30G) to draw the required volume. When reconstituting lyophilized peptide vials, aim the needle toward the inner glass wall and introduce solvent slowly, allowing it to trickle down without creating foam. Do not vortex or shake vigorously. Storage: Store sealed vials at room temperature (15°C to 30°C) shielded from direct light. Once punctured, preserve between 2°C and 8°C and utilize within 28 days. Discard if particulate matter, cloudiness, or discoloration is observed. Strictly for laboratory in-vitro investigation only.

1All peptide compounds cataloged are intended exclusively for laboratory research, biochemical assays, and analytical characterization. Strictly not for human, veterinary, diagnostic, or therapeutic administration.
2Analytical purity (≥99%) is validated via High-Performance Liquid Chromatography (HPLC) and Mass Spectrometry (MS). Compound integrity is dependent on adherence to cold-chain storage and inert handling protocols.
3The acquiring entity assumes sole responsibility for regulatory compliance, laboratory safety protocols, and safe handling in accordance with federal, state, and local standards. èvelan expressly disclaims liability for off-label or unapproved application.
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