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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
187847
187325
184320
180397
178186

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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
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)
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
Paolo Leva et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 44(1), 51-57 (2008-12-18)
The fate of the active ingredients of insecticide sprays after use in indoor environments was investigated. Indoor air sampling was performed through two types of adsorbents, namely, TENAX TA and XAD-2 (10 L). After sampling, both adsorbents were ultrasonically extracted
Xinghui Xia et al.
Chemosphere, 78(11), 1329-1336 (2010-02-02)
Carbonaceous sorbents including black carbon (BC) and carbon nanotubes have attracted research attention around the world because of their effects on bioavailability of hydrophobic organic compounds (HOCs) in sediments and soils. In this research, (14)C-labeled and unlabeled phenanthrene were spiked
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