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MilliporeSigma

13674-U

Supelpak™-2SV polymeric adsorbent

greener alternative

matrix styrene-divinylbenzene, 20-60 mesh, pkg of 1000g

Synonym(s):

xad-2

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About This Item

UNSPSC Code:
23151817
NACRES:
SB.52

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Product Name

Supelpak™-2SV, matrix styrene-divinylbenzene, 20-60 mesh, pkg of 1000 g

form

beads

packaging

pkg of 1000 g

Quality Level

100

sustainability

Greener Alternative Product

technique(s)

LPLC: suitable

surface area

~300 m2/g

matrix

styrene-divinylbenzene

matrix active group

polymer

particle size

20-60 mesh

pore size

~0.65 mL/g pore volume
90 Å mean pore size

application(s)

environmental

greener alternative category

DfS-Developed

separation technique

reversed phase

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This Item
13673-U14056-U13682-U
Supelpak™-2SV matrix styrene-divinylbenzene, 20-60 mesh, pkg of 1000 g

Supelco

13674-U

Supelpak™-2SV

Supelpak™-2SV matrix styrene-divinylbenzene, 20-60 mesh, pkg of 100 g

Supelco

13673-U

Supelpak™-2SV

Supelpak™-2SVM pkg of 500 g

Supelco

14056-U

Supelpak™-2SVM

Supelpak™-2SV matrix styrene-divinylbenzene, 20-60 mesh, pkg of 250 g

Supelco

13682-U

Supelpak™-2SV

particle size

20-60 mesh

particle size

20-60 mesh

particle size

20-60 mesh

particle size

20-60 mesh

matrix active group

polymer

matrix active group

polymer

matrix active group

polymer

matrix active group

polymer

pore size

~0.65 mL/g pore volume, 90 Å mean pore size

pore size

~0.65 mL/g pore volume, 90 Å mean pore size

pore size

~0.65 mL/g pore volume, 90 Å mean pore size

pore size

~0.65 mL/g pore volume, 90 Å mean pore size

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

matrix

styrene-divinylbenzene

matrix

styrene-divinylbenzene

matrix

Styrene-Divinyl-benzene

matrix

styrene-divinylbenzene

technique(s)

LPLC: suitable

technique(s)

LPLC: suitable, NMR: suitable

technique(s)

LPLC: suitable, thin layer chromatography (TLC): suitable

technique(s)

LPLC: suitable, NMR: suitable

Application

  • Supelpak™-2SV resin was used as column packing material to extract sesquiterpenes.[1]
  • Supelpak™-2SV resin was used in glass column as packing material to capture limonene.[2]
  • Supelpak™-2SV resin was used as packing material to capture the off gas for NMR analysis.[3]
  • Used as adsorbent in the extraction of organochlorine compounds by Soxhlet extraction technique
  • Adsorbent in the extraction of honey samples using column chromatography for HPLC analysis
  • Used in adsorption chromatography
Polyaromatic adsorbent resin for hydrophobic compounds up to MW 20,000: phenols, organic removal, surfactants, aroma compounds, antibiotic recovery. May be used as support catalyst or metals removal. For cleaned US EPA versions, see Supelpak-2 and Supelpak-2B.

Legal Information

Supelpak is a trademark of Sigma-Aldrich Co. LLC

General description

We are committed to bringing you Greener AlternativeProducts. This product is a Design for Sustainability (DfS) developed product,which belongs to one of the four categories of greener alternatives. Click here to view its DfS scorecard.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCX2519
MKCQ8745
MKCQ7836
MKCM3400
MKCL8487

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Grayson T Wawrzyn et al.
Methods in enzymology, 515, 83-105 (2012-09-25)
Fungi produce a myriad of terpenoids with a broad range of biological activities, many of which can be adapted to human use. This requires knowledge of the enzymes responsible for the biosynthesis of these compounds. Herein, we describe strategies for
Engineering cyanobacteria for the production of a cyclic hydrocarbon fuel from CO2 and H2O
Halfmann, Charles, Liping Gu, and Ruanbao Zhou
Green Chemistry, 16, 3175-3185 (2014)
Sean A Agger et al.
Journal of bacteriology, 190(18), 6084-6096 (2008-07-29)
Cyanobacteria are a rich source of natural products and are known to produce terpenoids. These bacteria are the major source of the musty-smelling terpenes geosmin and 2-methylisoborneol, which are found in many natural water supplies; however, no terpene synthases have

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