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HPLC Buffers

Heap of buffer salt crystals

Buffers are solutions of a weak acid and its conjugate base, or a weak base and its conjugate acid. In analytical chemistry, buffers are typically used in reversed-phase high performance liquid chromatography (RP-HPLC), when the sample contains acidic or basic functional groups. Buffers mitigate the influence of hydrogen/hydronium and hydroxide ions, subsequently reducing pH fluctuation.   


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HPLC (25)
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Formic acid 98 - 100%
5.43804

Formic acid 98 - 100%

for HPLC LiChropur

Sodium perchlorate monohydrate
56581

Sodium perchlorate monohydrate

suitable for HPLC, LiChropur, 99.0-101.0% (T)

Ammonium hydrogen carbonate
5.33005

Ammonium hydrogen carbonate

for LC-MS LiChropur

Acetic acid 100%
5.43808

Acetic acid

100%, for HPLC LiChropur

Triethylamine
81101

Triethylamine

suitable for HPLC, LiChropur, ≥99.5% (GC)

Triethylammonium bicarbonate buffer
18597

Triethylammonium bicarbonate buffer

1 M, suitable for HPLC, LiChropur

Potassium phosphate monobasic
57618

Potassium phosphate monobasic

suitable for HPLC, LiChropur, 99.5-101.0% (T)

Sulfuric acid 98%
5.43827

Sulfuric acid

98%, for HPLC LiChropur

Sodium acetate
79714

Sodium acetate

suitable for HPLC, LiChropur, 99.0-101.0% (NT)

Methanesulfonic acid
59510

Methanesulfonic acid

suitable for HPLC, LiChropur, ≥99.5% (T)

Sodium phosphate monobasic
52074

Sodium phosphate monobasic

suitable for HPLC, 99.0-101.0% (T)

Ammonium dihydrogen phosphate
5.43837

Ammonium dihydrogen phosphate

for HPLC LiChropur

Potassium phosphate dibasic
5.43839

Potassium phosphate dibasic

anhydrous for HPLC LiChropur

Sodium phosphate dibasic
5.43838

Sodium phosphate dibasic

anhydrous for HPLC LiChropur

Borate buffer
89273

Borate buffer

suitable for HPLC, LiChropur, 0.127-0.140 M

Potassium phosphate dibasic
59678

Potassium phosphate dibasic

suitable for HPLC, LiChropur, 99.0-101.0% (T)

Sodium chloride
5.43832

Sodium chloride

for HPLC LiChropur

Ethylenediaminetetraacetic acid disodium salt dihydrate
79884

Ethylenediaminetetraacetic acid disodium salt dihydrate

suitable for HPLC, LiChropur, 99.0-101.0% (KT)

Phosphoric acid solution
93752

Phosphoric acid solution

49.5-50.5%, suitable for HPLC, LiChropur

Ammonium phosphate dibasic
79762

Ammonium phosphate dibasic

suitable for HPLC, LiChropur, 99.0-101.0% (T)

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Related Resources


Mobile Phase Buffers

Proper buffer choice, in terms of buffering species, ionic strength, and pH, is the most critical step in RP-HPLC method development for ionic analytes. Ionic analyte retention in RP-HPLC is fundamentally effected by the pH of the mobile phase. Thus, pH control of the mobile phase in RP-HPLC is one of the most important parameters for effective analyte separation.

The typical pH range for reversed-phase separations on silica-based columns is between 2 to 8. The buffer must have a pKa close to the desired pH, since buffers control pH best at their pKa. As a rule of thumb, it is ideal to choose a buffer with a pKa value <2 units of the desired mobile phase pH. We offer HPLC grade buffers for a wide pH range for all your lab chromatographic requirements.

Factors to be considered while choosing a HPLC Buffer

Chemical Purity

The quality of mobile phase additives (buffers, salts, acids and bases) along with organic solvents utilized in an HPLC experiment must be adapted to the detector sensitivity and elution protocol. High-quality solvents and reagents are recommended for optimal chromatography.

Chemical Compatibility

Buffer composition along with mobile phase pH must be chosen in agreement with column housing material and nature of the stationary phase. This prevents damage to the column hardware and bed.

Buffer Solubility

Ideally, the buffer should be completely water soluble and should not precipitate. Buffer concentration must be carefully chosen to avoid precipitation at higher concentrations, when the buffer is blended with the organic solvent. If neglected, it can create operational problems in the pumps and instigate HPLC column blockage.

Buffer Strength

An eluent showing weak interaction with the stationary phase is only capable of eluting weakly bonded analytes from the column, whereas a strong interaction causes elution of strongly bonded sample molecules. The elution or solvent strength of various solvents depends on the type of stationary phase used. After the elution strength, the viscosity and UV absorbance of the buffer plays an important role in terms of their suitability for use in HPLC analyses. 



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