Technical articles

Common Types of Buffer Solutions

To use buffer solutions effectively, you need a concrete understanding of different buffering systems. Below are several common buffer solutions and their uses to help deepen your understanding of buffers.

Phosphate Buffer Solutions

Because phosphoric acid is triprotic, phosphate buffering pairs can be HPO/HPO₄⁻, HPO₄⁻/HPO², or HPO²/PO³. In biochemical systems, commonly used phosphate buffers are typically prepared from sodium or potassium salts of the HPO₄⁻/HPO²⁻/ pair. pH stability in solution is mainly maintained by the equilibrium:

HPO₄⁻ + HO  HPO² + HO, with an effective pH range of approximately 6.28.2.

In biochemical applications, NaCl or KCl is often added to prepare phosphate-buffered saline (PBS) (commonly available in two versions: without/with Ca² and Mg²).

PBS is compatible with many biological samples and is commonly used for solution preparation, sample washing, and short-term suspension. Note:

a) In systems involving Ca²/Mg², phosphate may precipitate; choose PBS without divalent cations according to your experimental purpose.

b) Cryopreservation of cells generally requires osmoprotectants (e.g., DMSO) and nutrients; PBS alone is not suitable as a standard freezing medium.

c) PBS does not rely on the COHCO₃⁻ buffer; it is suitable for washing/short holds, not for maintaining long-term cell culture.

Borate Buffer Solutions

Borate buffer systems commonly use boric acid (HBO)/tetrahydroxyborate (B(OH)₄⁻) as the principal acidbase pair, with the fundamental equilibrium:

HBO + HO  B(OH)₄⁻ + HO.

Typical formulations include borax buffer (based on sodium tetraborate, NaBO·10HO) and boric acidborax buffers (boric acid and borax mixed in defined ratios). The effective pH range is usually about 8.010.0 (commonly 7.59.5); the exact range depends on component ratios and ionic strength. For biochemical applications, an appropriate amount of NaCl may be added to maintain isotonicity.

Applications and notes: The pH range of the boric acid/borax system is adjacent to that of tear fluid; consequently, it is used in some ophthalmic drops as a pH/isotonicity adjuster (typically together with other buffering/osmotic agents). In addition, borax buffer can serve as a release or solubilizing medium for certain drugs (particularly those containing vicinal diol structures). Use cautiously or avoid in cell culture and in systems involving polyols/sugar assays.

Tris(hydroxymethyl)aminomethane–Hydrochloric Acid Buffer (Tris-HCl)




Tris (CH₁₁NO) is a weak base and commonly forms the Tris-HCl buffer with hydrochloric acid. Typically, dissolve Tris in water first, then adjust to the target pH with HCl; add NaCl if isotonicity is needed (TBS: Tris-buffered saline).


Buffering principle and range: The primary amine (–NH) in Tris is protonated to form the ammonium salt (R–NH₃⁺), which, together with the unprotonated form, constitutes the buffer pair: Tris·H + HO  Tris + HO, with an effective pH range of approximately 7.09.0. The pH of Tris-HCl is strongly affected by solution concentration and temperature, and alkaline Tris solutions readily absorb CO from air, causing pH to decrease; fresh preparation is recommended.

Additional note: Tris contains a primary amine and may interfere with coupling chemistries involving amines (e.g., NHS esters). Avoid Tris buffers in such experiments.

Applications: Tris exerts minimal interference in many biochemical processes and does not precipitate with Ca², Mg², or most heavy metal ions. It is commonly used for dissolving and extracting biological macromolecules such as DNA and proteins and also appears in certain biopharmaceutical formulations (refer to product labeling).

HEPES (4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid)

HEPES (CH₁₈NOS) is a Goods buffer and a zwitterionic molecule. Its buffering capacity arises mainly from reversible protonation/deprotonation at one amine site on the piperazine ring (pK  7.5 at 25 °C); the other amine contributes little near pH 7 ± 0.5. The sulfonic acid group is essentially fully dissociated to –SO₃⁻ at pH 7.27.6. Buffering capacity is maximal when the solution pH is close to the pK. To prepare, dissolve HEPES and fine-tune to the target pH with NaOH (or HCl). The effective pH range is about 6.8–8.2. Compared with many buffers, HEPES exhibits relatively small pH dependence on concentration and temperature and shows good pH stability.

In aqueous solution, the sulfonic acid group (–SOH) is essentially fully dissociated to SO₃⁻ under physiological pH, while buffering is actually provided by reversible protonation/deprotonation at the tertiary amine site (RN  RNH, pK  7.5 at 25 °C). Upon addition of acid, RN is protonated to RNH, consuming H and inhibiting a drop in pH; upon addition of base, RNH loses a proton to form RN, consuming OH and inhibiting a rise in pH. The resulting conjugate acid/base pair coexists in comparable amounts at pH  pK (HendersonHasselbalch relationship), yielding maximal buffering capacity. The distribution of chemical species shifts with pH: in the neutral region the zwitterion (–SO₃⁻ with RNH, overall neutral) predominates; under acidic conditions one or both amines become further protonated to give cations; under basic conditions both amines are unprotonated, giving an anion (–1). Thus, HEPES resists acid–base perturbations and stabilizes solution pH via a dynamic equilibrium between amine protonation states and bulk pH.

Applications and notes: HEPES has low cytotoxicity, crosses biological membranes poorly, and minimally perturbs many intracellular processes. It is suitable for open-air cell handling and microscopy (short operations outside a CO incubator) and for a broad range of nucleic-acid/protein experiments. In studies involving metals or material corrosion/degradation, evaluate potential interactions between HEPES and metal ions that may affect the system.

Aladdin-Related Product List

Product Name

CAS No.

Notes

Orthophosphoric acid (Phosphoric acid)

7664-38-2

Sodium dihydrogen phosphate

7558-80-7

Common hydrate: monohydrate 10049-21-5

Disodium hydrogen phosphate

7558-79-4

Common hydrate: dodecahydrate 10039-32-4

Potassium dihydrogen phosphate (KHPO)

7778-77-0

Dipotassium hydrogen phosphate (KHPO)

7758-11-4

Boric acid

10043-35-3

Sodium tetraborate decahydrate (borax)

1303-96-4

Related: anhydrous 1330-43-4

Tris (tris(hydroxymethyl)aminomethane)

77-86-1

Tris·HCl (tromethamine hydrochloride)

1185-53-1

4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid

7365-45-9

Sodium chloride

7647-14-5

PBS component

Potassium chloride

7447-40-7

Optional PBS component

Hydrochloric acid

7647-01-0

For pH adjustment

Sodium hydroxide

1310-73-2

For pH adjustment

 

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Categories: Technical articles
Explore topics: Buffer Solutions

Da — when not otherwise indicated, molecular weight units are daltons.   Mw — weight-average molecular weight.   Mn — number-average molecular weight.

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Cite this article

Aladdin Scientific. "Common Types of Buffer Solutions" Aladdin Knowledge Base, updated Nov 5, 2025. https://www.aladdinsci.com/us_en/faqs/common-types-of-buffer-solutions-en.html
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