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10357

Supelco

Amberlite™ XAD®-2

pkg of 500 g

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About This Item

CAS Number:
9003-70-7
UNSPSC Code:
23151817

form

beads (small)

packaging

pkg of 500 g

availability

not available in (Currently experiencing backorder delays due to raw material supply disruption)

technique(s)

HPLC: suitable
LPLC: suitable

surface area

~300 m2/g

matrix

styrene-divinylbenzene (macroreticular)

matrix active group

polymer

particle size

20-60 mesh

pore size

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

density

1.02 g/mL at 25 °C (true wet)(lit.)
1.08 g/mL at 25 °C (skeletal)(lit.)

separation technique

reversed phase

storage temp.

2-8°C

InChI

1S/C24H27NO5/c1-24(2,3)30-22(27)13-12-16(14-26)25-23(28)29-15-21-19-10-6-4-8-17(19)18-9-5-7-11-20(18)21/h4-11,14,16,21H,12-13,15H2,1-3H3,(H,25,28)/t16-/m0/s1

InChI key

BCIPGSZQUDLGSY-INIZCTEOSA-N

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General description

Amberlite XAD-2, a hydrophobic copolymer of styrene-divinylbenzene resin, requires longer purification process and is used as a sorbent. Amberlite XAD-2 resin depending upon the aromaticity and size of the hydrophobic groups sorbs organic compounds through low-energy physical interactions.
Nonionic macroreticular resin that adsorbs and releases ionic species through hydrophobic and polar interactions; usually used under isocratic conditions.
Specifications:

Application

Amberlite™ XAD®-2 was used:
  • as adsorbent in the extraction of organochlorine compounds using Soxhlat extraction technique
  • as adsorbent in the extraction of honey samples using column chromatography for HPLC analysis
  • 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 for catalyst or metals removal. For cleaned US EPA versions, see Supelpak-2 and Supelpak-2B.
     

Legal Information

Amberlite is a trademark of DuPont de Nemours, Inc.
XAD is a registered trademark of The Dow Chemical Company or an affiliated company of Dow

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
190735
187847
187325
184320
180397

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M Tamura et al.
The Journal of biological chemistry, 260(17), 9672-9677 (1985-08-15)
Na+,K+-ATPase inhibitors have been found to exist in acutely saline-infused hog plasma, which also inhibit the specific binding of ouabain to Na+,K+-ATPase and the binding of digoxin to specific anti-digoxin antibody. Two of these inhibitors were purified by a combination
I Martos et al.
Journal of agricultural and food chemistry, 48(5), 1498-1502 (2000-05-23)
European Eucalyptus honeys showed a common and characteristic HPLC profile in which the flavonoids myricetin (3,5,7,3',4', 5'-hexahydroxyflavone), tricetin (5,7,3',4',5'-pentahydroxyflavone), quercetin (3,5,7,3',4'-pentahydroxyflavone), luteolin (5,7,3', 4'-tetrahydroxyflavone), and kaempferol (3,5,7, 4'-tetrahydroxyflavone) were identified. Their contents, and relative amounts, in the analyzed honey samples
Trapping efficiency of polyurethane foam and Amberlite XAD-2 for various organochlorine compounds
Nerin, C., et al.
Fresenius Journal of Analytical Chemistry, 352, 609-611 (1995)
Vinod K Jain et al.
Talanta, 79(5), 1331-1340 (2009-07-29)
Two novel azocalix[4]pyrrole Amberlite XAD-2 polymeric chelating resins were synthesized by covalently linking diazotized Amberlite XAD-2 with calix[4]pyrrole macrocycles. The chelating resins were used for extraction, preconcentration and sequential separation of metal ions such as Cu(II), Zn(II) and Cd(II) by
Ayako Kanno et al.
The Journal of toxicological sciences, 35(6), 817-826 (2010-12-09)
Amberlite XAD-2 resin extracts of river and drinking water sampled from the Northwest district of Chiba Prefecture in each month during the period from January to December 2008 were investigated to characterize and determine their mutagenic potentials and polycyclic aromatic
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