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13682-U

Supelco

Supelpak™-2SV

matrix styrene-divinylbenzene, 20-60 mesh, pkg of 250 g

Synonym(s):

xad-2

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About This Item

UNSPSC Code:
23151817
NACRES:
SB.52

form

beads

Quality Level

100

packaging

pkg of 250 g

technique(s)

LPLC: suitable
NMR: 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

separation technique

reversed phase

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General description

Supelpak™-2SV is purified Amberlite™ XAD2 that has been specially cleaned and tested for optimal performance in the capturing and extraction of semivolatile organics. Packaged in glass containers.

Application

  • Supelpak™-2SV resin was used as column packing material to extract sesquiterpenes.
  • Supelpak™-2SV resin was used in glass column as packing material to capture limonene.
  • Supelpak™-2SV resin was used as packing material to capture the off gas for NMR analysis.

Legal Information

Amberlite is a trademark of DuPont de Nemours, Inc.
Supelpak is a trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCG1384
MKCK1710

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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
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

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