Laboratory ancillaries

Popular product

BAC Water

Also known as Bacteriostatic Water

Benzyl-alcohol-preserved aqueous laboratory diluent · nominal composition must be verified per lot

Component-specific · Batch COACAS 7732-18-5RUO
Batch COA
MOQ1 kit (10 vials) per SKU
Supplied formNon-peptide aqueous ancillary; water plus a lot-specified benzyl-alcohol preservative concentration
Lead time7–14 days
BAC Water — Lot-specific clear aqueous material; confirm colour, clarity and particulate specification on the released-batch COA
BAC Water — Lot-specific clear aqueous material; confirm colour, clarity and particulate specification on the released-batch COA · Representative packaging image · verify the ordered lot
Representative packaging image · verify the ordered lot

Decision summary

Key benefits

  • Laboratory applications include preserved aqueous diluent studies, formulation screening, container-closure workflows and method development where a defined benzyl-alcohol concentration is appropriate
  • Preservative activity may reduce microbial proliferation under validated conditions, but it does not sterilize a contaminated vial or establish analyte stability.
Published research context is presented for literature orientation only. It is not a dosing, treatment or human-use instruction.

Qualification data

Specifications to confirm against the released lot

CAS
7732-18-5
Formula
Not applicable — mixture or multi-component material
Molecular weight
Component-specific; no single molecular weight
Appearance
Lot-specific clear aqueous material; confirm colour, clarity and particulate specification on the released-batch COA
Purity
Component-specific released results; confirm water grade and benzyl-alcohol assay on the batch COA · target, verify batch COA
Storage
Follow the released lot COA, SDS, label and stability statement. Temperature, light protection, container orientation, first-access period and excursion limits depend on the exact water grade, preservative concentration, container-closure system and claimed microbiological quality. Do not transfer storage instructions from Pfizer/Hospira or another finished product unless the offered lot is that labelled product.
MOQ
1 kit (10 vials) per SKU
Lead time
7–14 days

Qualification matrix

Identity, purity and content are separate release questions.

Identity

Confirm the stated molecule and supplied form. Start with the matching batch COA; request sequence-level evidence only when the buyer's written procedure requires it and availability or a separate scope has been agreed.

Purity

Review RP-HPLC method conditions, wavelength, integration and related-peak handling. A percentage without the method is not enough.

Stability

Follow the storage condition stated on the batch COA or label from receipt onward.

Research context

What researchers study about BAC Water

“Bacteriostatic water” generally denotes water containing a preservative, commonly benzyl alcohol. Approved Bacteriostatic Water for Injection products have product-specific labels, concentrations, containers and microbiological controls. An RUO ancillary with a similar name is not automatically USP-compliant, sterile, nonpyrogenic or injectable. Procurement should specify water grade, benzyl-alcohol concentration, pH, container closure, chemical assays and any separately claimed sterility, endotoxin or bioburden limits.

  • Laboratory formulation and reconstitution-method development, preservative-compatibility studies, analytical sample preparation and ancillary qualification
  • These are laboratory applications, not clinical indications.

Mechanism context

The question the literature is testing

Benzyl alcohol is used as a bacteriostatic preservative: at an appropriate concentration it can inhibit microbial growth through membrane and protein effects. Bacteriostatic is not bactericidal or sterilizing. Water is the solvent component, while peptide dissolution, chemical stability and assay performance depend on the complete formulation and handling conditions. No universal mixing, swirling or injection instruction is provided.

Evidence map

Research routes and exposure context

Evidence tierAnalytical / laboratory context
Routes reported in sources
No administration route applies
Dose / exposure contextProtocol-specific; verify the cited primary source
Routes and exposure contexts summarize cited studies or approved finished-product labels. They are not instructions for administering this RUO material; no customer dose is provided.

Evidence boundaries

Compatibility, limitations and decision context

  • For laboratory use only
  • Follow the lot SDS and institutional chemical and microbiological controls
  • Benzyl alcohol has recognized systemic toxicity and labelled Bacteriostatic Water for Injection products warn against neonatal use, but this toxicology context is not an administration instruction
  • Preservative content does not establish sterility or permit use of a compromised container
  • This catalogue provides no injection, aseptic-puncture or patient-use procedure.

Interactions reported in the literature

  • Compatibility is analyte-, concentration-, pH-, buffer-, container- and method-specific
  • Benzyl alcohol may be incompatible with some peptides, proteins, cells or analytical endpoints
  • Preservative-free water is not automatically interchangeable; use direct stability and performance evidence for the intended system.
Literature context is not a supplier release result or human-use instruction. Follow your institution's approved laboratory risk assessment.

Batch documentation

BAC Water batch COAs

Laboratory: Manufacturer's QC laboratory

  • Blurred preview of a BAC Water 3 mL batch COA3 mL
  • Blurred preview of a BAC Water 10 mL batch COA10 mL

Previews are blurred on purpose so the documents cannot be reused; third-party reports show their first page only. Sales sends the clear full version for the product and strength you ask about.

Independent test fails? Full refund.

Representative records, refreshed periodically

Published COAs show recent representative batches and may not be the newest. For a quote or shipment, sales confirms the lot and sends its COA.

Third-party reports, added progressively

Previews of the first page of third-party reports are on our Quality page and on the matching product pages; sales sends the full report on request. You can also send any vial from your order to an independent laboratory of your choice. Unless agreed otherwise in writing, the buyer pays for optional testing.

Help reviewing your COA

Need help reading a batch COA or third-party report? Sales can explain the test items, specifications and how the results relate to the lot under discussion.

On every batch COA: Batch COA · Verify LyoPep

Ask for the current packet, not a generic certificate

  • Require water grade, benzyl-alcohol identity and quantitative content, relevant chemical limits, visible-particle criteria, fill volume, container-closure specification, traceable lot and stability basis
  • If sterility, bacterial endotoxin or bioburden is claimed, require separate released-lot results with named methods and acceptance limits
  • Clear colourless appearance alone cannot prove composition, microbiological quality or suitability.
Batch COA for the released lotHPLC purity with method contextMS identity resultEndotoxin resultFill amount (measured content per vial)SDS and handling statement

Available fills

Quote the fill and pack configuration you need

Reference SKUFillBase pack
BAC33 ml10 vials
BAC55 mL10 vials
BAC1010 ml10 vials
BAC3030 ml25 vials

Handling

Plan storage before the parcel arrives

Follow the released lot COA, SDS, label and stability statement. Temperature, light protection, container orientation, first-access period and excursion limits depend on the exact water grade, preservative concentration, container-closure system and claimed microbiological quality. Do not transfer storage instructions from Pfizer/Hospira or another finished product unless the offered lot is that labelled product.

State the destination and timing so receipt can be planned, then move the material into its stated storage condition on arrival.

Buyer FAQ

Terms to settle before the purchase order

Can a buyer arrange third-party testing?+

Yes. You can send any vial from your order to an independent laboratory of your choice. If you want the laboratory, specification, sampling, method and acceptance rule agreed with us before testing, sales confirms them in writing. Unless otherwise agreed in writing, the buyer pays the cost of this optional testing.

What if my own lab test shows the product is out of specification?+

Send any vial from your order to an independent laboratory of your choice. If the report shows the product does not meet the specification on its COA — purity below the stated minimum, or an identity that does not match — share the report with our sales team and we refund that product in full.

Does HPLC purity prove peptide content?+

No. Chromatographic purity describes the relative peak profile under a stated method. Identity, water, counter-ion, residual solvents and assay/content may require separate methods.

How should material be stored after delivery?+

Move it into the storage condition stated on the batch COA or label as soon as it arrives, and record the package condition on receipt.

How are payment terms handled?+

Available methods and milestones depend on order value, destination and project type. The pro forma invoice should state currency, bank details, fees, payment milestones and the release condition.

Why must the testing laboratory understand peptide chemistry?+

Free-base and salt forms, hydrophilic and hydrophobic sequences, aggregation and adsorption can change sample preparation and method suitability. Use a laboratory experienced with the molecule class.

These are buyer-qualification references, not claims that this RUO material is regulated, certified or released under those frameworks. Applicability depends on the buyer's workflow and jurisdiction.

Selected sources

Literature behind the research context

  • Component identity: NIH PubChem CID 962 identifies water and CID 244 identifies benzyl alcohol as C₇H₈O, 108.14 g/mol and CAS 100-51-6; component records do not define the supplied blend.
  • Product-specific labelling: DailyMed records for approved Bacteriostatic Water for Injection products identify their own benzyl-alcohol concentration, pH, container and warnings. A 0.9% label and a 1.1% label are distinct records or presentations, not interchangeable proof for this RUO lot.
  • Multi-dose-vial context: current CDC Injection Safety guidance states that an opened, labelled multi-dose vial is generally discarded within 28 days unless the manufacturer states another date. This does not establish sterility, approved multi-dose status or peptide stability for an RUO vial.
  • Neonatal toxicology: Gershanik et al., N Engl J Med. 1982, PMID 7133084, documents fatal neonatal toxicity associated with benzyl-alcohol exposure; this is safety context, not an administration instruction.
  • Current allergy context: Le and Wu, Dermatitis. 2026, PMID 41649135, reviews benzyl alcohol as a potential contact allergen.
  1. 01

    The Gasping Syndrome and Benzyl Alcohol Poisoning

    New England Journal of Medicine · 1982 · peer-reviewed original research (landmark clinical report)

    Open source
  2. 02

    Toxicity of Benzyl Alcohol in Adult and Neonatal Mice

    Journal of Pharmaceutical Sciences · 1986 · peer-reviewed original research (animal toxicology)

    Open source
  3. 03

    Benzyl Alcohol: Allergen of the Year 2026

    Dermatitis (official journal of the American Contact Dermatitis Society) · 2026 · peer-reviewed review (society-commissioned 'Allergen of the Year' designation)

    Open source
  4. 04

    Bacteriostatic Water Injection, USP -- 0.9% Benzyl Alcohol Product Label

    DailyMed (US National Library of Medicine) / FDA-approved manufacturer label · 2014 · regulatory document (FDA-approved manufacturer package insert, hosted on DailyMed)

    Open source
  5. 05

    Preventing Unsafe Injection Practices

    CDC Injection Safety · 2026 · public-health guidance

    Open source
  6. 06

    PubChem Compound Summary: Benzyl Alcohol (CID 244)

    NIH PubChem · 2026 · authoritative chemical database

    Open source

Product FAQ

Questions buyers ask about BAC Water

How should a laboratory choose between preserved and preservative-free water?+

Follow the exact method or formulation specification being replicated. Benzyl alcohol can change peptide stability, adsorption, assay response and cell compatibility, so a preserved diluent is not universally interchangeable with preservative-free water. Confirm the supplied preservative concentration, peptide/formulation compatibility, container and intended analytical endpoint; do not infer injectable suitability from the word “bacteriostatic”.

Which documents should support a preserved aqueous diluent?+

The batch package should state water grade, benzyl-alcohol identity and quantitative assay, other relevant chemistry, visible-particle criteria, fill volume, container-closure details, lot and expiry or retest basis. Sterility, bacterial endotoxin and bioburden are different tests and should be reported only when performed with named methods and acceptance limits. A clear appearance or preservative assay cannot prove sterility.

Evidence before order

Buyer intelligence