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Supelco

SP®-2331 Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.20 μm

Synonym(s):

SP-2331, 30M .25MM .20UM

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About This Item

UNSPSC Code:
41115710
eCl@ss:
32119290

material

fused silica

Agency

suitable for EPA 1613

parameter

≤25-275 °C temperature (isothermal or programmed)

Beta value

313

df

0.20 μm

technique(s)

gas chromatography (GC): suitable

L × I.D.

30 m × 0.25 mm

application(s)

agriculture
environmental
food and beverages

column type

capillary highly polar

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General description

Application: A highly polar cyanosiloxane column specially tested for analyses of dioxins, specifically tetrachlorodibenzodioxin (TCDD) isomers. Because the phase is stabilized, it has a maximum temperature slightly higher than non-bonded cyanosiloxane columns.
USP Code: None
Phase:
  • Stabilized
  • Proprietary
Temp. Limits:
  • Subambient to 275 °C (isothermal or programmed)

Application

SP® 2331 capillary column may be used in in high-resolution gas chromatography coupled with mass selective detection (HRGC-MSD) for selective separation of 2, 3, 7, 8-tetrachlorodibenzofuran. It was also used in HRGC-MSD for the analysis of chlorinated biphenyls, chlorinated dibenzodioxins, and chlorinated dibenzofurans. It was also used in the gas chromatographic separations of pyrethroid insecticides allethrin and cypermethrin in various achiral and chiral stationary phases.

Other Notes

We offer a variety of chromatography accessories including analytical syringes

Legal Information

SP is a registered trademark of Sigma-Aldrich Co. LLC

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Agriculture and Soil Pollution.
Nature, 41-44 (2005)
Selective separation of 2, 3, 7, 8-tetrachlorodibenzofuran by high-resolution gas chromatography and by alumina column liquid chromatography.
Ballschmiter K
Analytical Chemistry, 59 (20), 2536-2538 (1987)
Diastereoselective and enantioselective chromatography of the pyrethroid insecticides allethrin and cypermethrin.
Kutter JP and Class TJ.
Chromatographia, 33 (3-4), 103-112 (1992)
The determination of chlorinated biphenyls, chlorinated dibenzodioxins, and chlorinated dibenzofurans by GC-MS.
Karlheinz B
Journal of High Resolution Chromatography, 15 (4), 260-270 (1992)
Anna Malmvärn et al.
Environmental science & technology, 39(21), 8235-8242 (2005-11-22)
Polybrominated dibenzo-p-dioxins (PBDDs) are known to be formed as byproducts in connection with the manufacture and combustion of products containing brominated flame retardants. However, to date little is known about the occurrence of PBDDs in biological samples. The aim of

Related Content

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

Chromatograms

suitable for GC

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