HPLC Method for Analysis of  Sucrose octasulfate on BIST A+  Column

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Description

· HPLC Method for Analysis of [compouneds] on BIST A+ Column by SIELC Technologies

Sucrose octasulfate is a chemical compound derived from sucrose, a common sugar, with the chemical formula C 12 H 22 O 35 S 8 . It is characterized by the substitution of eight sulfate groups for hydroxyl groups in the sucrose molecule. This modification significantly changes the properties of the original sugar molecule, making sucrose octasulfate more complex and specialized in its applications.

In terms of its structure, sucrose is a disaccharide composed of glucose and fructose units. When these hydroxyl groups are replaced with sulfate groups in sucrose octasulfate, the molecule becomes highly polar and acidic due to the presence of sulfate groups, which are strong acid residues.

You can find detailed UV spectra of Sucrose octasulfate and information about its various lambda maxima by visiting the following link .

Using SIELC’s newly introduced BIST™ method, sucrose octasulfate can be retained on a negatively-charged, cation-exchange BIST A+ column. There are two keys to this retention method: 1) a multi-charged, positive buffer, such as TMEDA formate, which acts as a bridge, linking the negatively charged dye to the negatively-charged column surface and 2) a mobile phase consisting mostly of organic solvent (such as MeCN) to minimize the formation of a solvation layer around the charged analytes. Using this new and unique analysis method, oligonucleotide can be separated, retained, and detected at ELSD

Method Parameters

Mobile PhaseGradient MeCN – 70-40%, 15 min
BufferDMP acetate pH 4.0 – 5 mM
Flow Rate0.4 ml/min
DetectionELSD, the nebulizer and evaporator temperatures 70°C,with a gas flow rate of 1.6 Standard Liters per Minute (SLM
Sample1 mg/ml in MeCN/H2O – 50/50%
Injection volume5 µl
Class of CompoundsSulfated polysaccharides
Analyzing CompoundsSucrose octasulfate

HPLC Column Used

BIST A+, 2.1 x 100 mm, 5 µm, 100 A, dual ended