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Aūra BAC Water

Aūra BAC Water

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Description

Aūra BAC Water is bacteriostatic water for research use, formulated with 0.9% benzyl alcohol as a preservative. It is used as a sterile diluent for reconstituting lyophilized materials in controlled laboratory environments.

Research Characteristics:

  • Sterile diluent for reconstitution of research peptides and other lyophilized materials.
  • Contains benzyl alcohol to help inhibit microbial growth in multi-use research vials.
  • Intended for use in controlled laboratory environments under appropriate research protocols.
Strength
30 mL
Appearance
Clear sterile solution
CAS Number
100-51-6 (benzyl alcohol)
Molecular Formula
C₇H₈O
Molecular Weight
108.14 g/mol
SKU
AURA-BAC-30
Category
Research Diluent
Stock Status
● Only 24 vials left
!

THIS PRODUCT IS INTENDED AS A RESEARCH CHEMICAL ONLY

This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only. Bodily introduction of any kind into humans or animals is strictly forbidden by law. This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused, or mislabeled as such.

Always quality-tested, verified with third-party COAs

At every stage, Aūra Peptides batches are screened by independent labs for identity, purity, sterility, and endotoxins. Each lot is released only after it meets strict research-grade specifications and is backed by a third-party Certificate of Analysis (COA) for full transparency.

This multi-step process helps ensure that what’s on the label is exactly what’s in the vial—so researchers can focus on data, not doubt.

Identity Test

Passed

Verifies the peptide’s sequence and structure so the correct compound is present in each vial.

Purity Test

Passed

Measures purity and concentration to confirm ≥99% purity on qualifying batches.

Sterility Test

Passed

Screens for bacteria, fungi, and other microorganisms to verify sterile handling.

Endotoxicity

Passed

Tests for lipopolysaccharides (LPS) to ensure endotoxin levels stay within research limits.

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