HPLC Method for Separation of Amines on BIST B and BIST B+ Columns

HPLC Method for Separation of Amines on BIST B and BIST B+ Columns by SIELC Technologies

Separation type: Bridge Ion Separation Technology, or BIST™ by SIELC Technologies

HPLC Method for Separation of of Amines on BIST B and BIST B+ Columns by SIELC Technologies
HPLC Method for Separation of Amines on BIST B and BIST B+ Columns by SIELC Technologies

m-Xylylenediamine (MXDA) is a popular curing agent used on epoxy resins. 2,4,6-Tris(dimethylaminomethyl)phenol is another amine-based curing agent used on epoxy resins. Using SIELC’s newly introduced BIST™ method, these amines can be retained and separated on a positively charged, anion-exchange BIST™ B or BIST™ B+ column. The surface chemistry of BIST™ B+ columns are designed to have stronger ionic retention capabilities, resulting in the marked increase in retention compared to BIST™ B columns.

There are two keys to this retention method: 1) a multi-charged, negative buffer, such as Sulfuric acid (H2SO4), which acts as a bridge, linking the positively charged dipeptide to the positively 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, these two amines can be UV detected at 210 nm.

High Performance Liquid Chromatography (HPLC) Method for Analysis of Amines

Condition

ColumnBIST B, 3.2 x 100 mm, 5 µm, 100 A
Mobile PhaseMeCN – 70%
BufferH2SO4 – 0.2%
Flow Rate0.5 ml/min
DetectionUV 210 nm
Peak Retention Time

Description

Class of CompoundsAmines
Analyzing Compoundsm-Xylylenediamine, 2,4,6-Tris(dimethylaminomethyl)phenol

Application Column

BIST B

Column Diameter: 3.2 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

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BIST B+

Column Diameter: 3.2 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
2,4,6-Tris(dimethylaminomethyl)phenol
m-Xylylenediamine
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.