We report net peptide content, not just purity — so the milligrams you dose aren't padded with water and counter-ion. RP-HPLC purity and ESI-MS identity, on a lot-numbered COA.
Net peptide content, not just purity — RP-HPLC + ESI-MS, lot-numbered COA.
Net peptide content on every lot's COA.
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0.9% benzyl-alcohol bacteriostatic reconstitution diluent (multi-use)
Overview
Bacteriostatic Water for Injection (BAC Water) is sterile water containing 0.9% benzyl alcohol as a preservative, used as a multi-use reconstitution diluent. The benzyl-alcohol preservative inhibits microbial growth in a vial whose septum has been pierced repeatedly, supporting multi-dose use over the conventional ~28-day window after first puncture (the USP-compendial expectation for preserved injectable solutions). For preservative-compatible peptides it is the workhorse diluent in workflows where a single vial supports many small aliquots over a multi-week period. It is supplied as a characterized ancillary diluent rather than a research-target molecule. Lyochem supplies BAC Water in sterile vial formats prepared from pharmaceutical-grade benzyl alcohol and Water for Injection, with the benzyl-alcohol content documented explicitly on the label and release packet alongside sterility and endotoxin data. BAC Water is not universally compatible: some short peptides interact with benzyl alcohol, and for those preservative-free Sterile Water for Injection in single-use aliquots is the recommended alternative. Confirm the recommended diluent for the specific peptide on its COA before defaulting to BAC Water.
Applications & buyer fit
Solvents and ancillaries are the bench-support consumables a lab pairs with a reference standard once it leaves the freezer — bacteriostatic and sterile water, isotonic saline, 0.6% acetic-acid water, and glacial acetic acid for in-house diluent prep. These are diluents and process auxiliaries rather than research targets, so the documentation is diluent / solvent-grade (component identity, sterility, endotoxin, pH / osmolality, pharmacopeia monograph) rather than the peptide HPLC + MS + sequence packet. Diluent selection follows the peptide's stability profile: acidic-pH-requiring proteins use the acetic-acid water; preservative-incompatible peptides use sterile water; preservative-compatible peptides for multi-use vials use BAC water.
Academic Laboratories
Universities, medical schools, and government research institutes qualifying a reference standard for a method-development or in vivo workflow.
Core Facilities & Instrumentation Cores
Shared instrumentation cores, mass-spec facilities, and departmental analytical labs holding reference standards for cross-PI method validation and reagent qualification.
Contract Research Organisations (CROs)
CROs running preclinical and translational studies on behalf of academic, biotech, or pharma sponsors who need traceable reference material across multi-site campaigns.
Every release ships with its own batch-specific CoA — identity, purity, and the analytical scope agreed at quote stage, tied to the exact lot you receive.
Review a representative batch CoA before you order, so you can confirm the packet matches what your method or sponsor audit needs.
Supplied strictly as a research reagent to research institutions — not a finished dosage form and not for human administration. Buyer qualification runs at the inquiry stage.
Specifications
Documentation available on request
Regulatory note
Reconstitution diluent containing benzyl-alcohol preservative; supplied for Research Use Only. Not universally compatible with all peptides — some require preservative-free SWFI. Verify sterility, endotoxin, and injectable-grade compliance with the destination market's requirements before use.
Frequently asked questions
The benzyl-alcohol concentration is stated explicitly on the product label and the release packet, alongside sterility and endotoxin data, so a lab can check preservative compatibility against its specific peptide before the vial is opened. This matters because some short peptides interact with benzyl alcohol, and for those the documented preservative-free Sterile Water for Injection is the alternative diluent. The recommended diluent for a given reference standard is noted on that standard's own COA, so the pairing is traceable rather than assumed.
Per USP convention it is the expected window for preserved injectable solutions and a conservative operational default, not a hard per-peptide limit. The 0.9% benzyl alcohol suppresses microbial growth after repeated septum punctures, which supports the multi-use window, but the actual in-solution stability of a specific peptide-in-diluent combination is an empirical question for the lab's own protocol: some warrant a shorter window, others tolerate longer. The 28-day default suits most reference-standard reconstitutions held refrigerated, with peptide-specific stability confirmed against the intended assay.
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