p-Toluenesulfonic acid
Column: | Amaze HA |
Separation Modes: | reveresed-phase , anion-exchange |
Column Dimenstions: | 4.6x100, 3 um, 100A |
Mobile Phase: | "A: 2% ACN with 40 mM ammonium phosphate pH 4.0 B: 20% ACN with 100 mM ammonium phosphate pH 2.0 gradient from 100% A to 100% B in 15 minutes, 5 minutes hold " |
Detection: | 205 nm |
Sample: | 0.2-0.5 mg/ml |
Injection: | 2 uL |
Flow rate: | 1 ml/min |
Class of compounds: | Aromatic acid, Isomer, Organic acid, Organic compound, Preservative, Supplement, Vitamin |
Nature of compounds: | Acidic, Hydrophilic, Hydrophobic, Neutral, Polar |
Compounds: | Acetic acid, Ascorbic acid, Formic acid, Succinic acid, Citric acid, Malonic acid, Fumaric acid, Mandelic acid, Oxalic acid, Terephthalic acid, Benzoic acid, Maleic acid, Phthalic acid, Benzenesulfonic acid, p-Toluenesulfonic acid |
Column: | Heritage MA |
Separation Modes: | RP, anion-exchange |
Column Dimenstions: | 4.6x50 mm, 3 um, 100A |
Mobile Phase: | ACN with AmFm pH 3 |
Detection: | UV 255 nm |
Sample: | 0.2 mg/ml |
Injection: | 3 uL |
Flow rate: | 1 ml/min |
Class of compounds: | Aromatic acid, Organic acid, Organic compound |
Nature of compounds: | Acidic, Hydrophilic, Hydrophobic, Neutral, Polar |
Compounds: | Benzenesulfonic acid, p-Toluenesulfonic acid, 2-Naphthalenesulfonic acid |
Column: | Heritage MA |
Separation Modes: | RP, anion-exchange |
Column Dimenstions: | 4.6x50 mm, 3 um, 100A |
Mobile Phase: | ACN with AmFm pH 3 |
Detection: | UV 255 nm |
Sample: | 0.2 mg/ml |
Injection: | 3 uL |
Flow rate: | 1 ml/min |
Class of compounds: | Aromatic acid, Organic acid, Organic compound |
Nature of compounds: | Acidic, Hydrophilic, Hydrophobic, Neutral, Polar |
Compounds: | Benzenesulfonic acid, p-Toluenesulfonic acid, 2-Naphthalenesulfonic acid |
Benzenesulfonic and toluenesulfonic acids are common organic acids used as counter-ions in pharmaceutical industry. Both acids are hydrophilic in nature with strong acidic properties. When traditional RP columns are used, poor retention and peak shape are observed due to non-specific secondary interactions. We developed a robust mixed-mode approach for the separation of benzenesulfonic acid and p-toluenesulfonic acid on the Amaze TR reversed-phase anion- and cation-exchange column. Both acids are retained by a weak reversed-phase mechanism and strong anion-exchange mechanism. The elution of these compounds is controlled by the amount of pH of the buffer, concentration of ions and the amount of acetonitrile in the mobile phase. The method is reproducible and effective with a good retention control and peak shape. It is compatible with major detection techniques including mass spectrometry (MS), Evaporative Light Scattering Detection(ELSD), ultraviolet detection and refractive index detection.
Column: | Amaze TR |
Separation Modes: | reversed-phase, anion-exchange |
Column Dimenstions: | 4.6x50 mm, 5 um, 100A |
Mobile Phase: | 20% ACN with 15 mM AmFm pH 3 |
Detection: | UV 255 nm |
Sample: | 0.3 mg/ml |
Injection: | 3 ul |
Flow rate: | 1 ml/min |
Class of compounds: | Organic acid, Organic compound |
Nature of compounds: | Acidic, Hydrophilic, Neutral, Polar |
Compounds: | Benzenesulfonic acid, p-Toluenesulfonic acid |