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10357

Supelco

Amberlite XAD®-2

pkg of 500 g

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CAS Number:

form

beads (small)

Quality Level

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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This Item
2027552672-U3025-U
Supelco

Supelco

10357

Amberlite XAD®-2

Supelco

Supelco

20275

Amberlite XAD®-2

Supelco

Supelco

52672-U

Amberlite XAD®-2

Supelco

Supelco

3025-U

Amberlite XAD®-2

packaging

pkg of 500 g

packaging

pkg of 100 g

packaging

pkg of 10 kg

packaging

pkg of 25 kg

technique(s)

HPLC: suitable, LPLC: suitable

technique(s)

HPLC: suitable, LPLC: suitable

technique(s)

HPLC: suitable, LPLC: suitable

technique(s)

HPLC: suitable, LPLC: suitable, ion chromatography: suitable

matrix

styrene-divinylbenzene (macroreticular)

matrix

styrene-divinylbenzene (macroreticular)

matrix

styrene-divinylbenzene (macroreticular)

matrix

styrene-divinylbenzene (macroreticular)

matrix active group

polymer

matrix active group

polymer

matrix active group

polymer

matrix active group

polymer

particle size

20-60 mesh

particle size

20-60 mesh

particle size

20-60 mesh

particle size

20-60 mesh

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 The Dow Chemical Company or an affiliated company of Dow
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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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)
Tim J Causon et al.
Journal of chromatography. A, 1217(21), 3519-3524 (2010-04-21)
Alternative approaches to conventional acetonitrile gradient methods for reversed-phase liquid chromatographic analysis of intact proteins have been investigated using commercial poly(styrene-co-divinylbenzene) monolithic columns (Dionex ProSwift RP-2H and RP-4H). Alternative solvents to acetonitrile (2-propanol and methanol) coupled with elevated temperatures demonstrated
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