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20275
Amberlite™ XAD®-2
pkg of 100 g
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Product Name
Amberlite™ XAD®-2, pkg of 100 g
SMILES string
N([C@@H](CCC(=O)OC(C)(C)C)C=O)C(=O)OCC1c2c(cccc2)c3c1cccc3
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
agency
suitable for ASTM® D4861
suitable for EPA Method 10A, Method 23 and OTM-45
form
solid
packaging
pkg of 100 g
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
Quality Level
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Related Categories
1 of 4
This Item | 10357 | SU853005 | 52672-U |
|---|---|---|---|
| matrix styrene-divinylbenzene (macroreticular) | matrix styrene-divinylbenzene (macroreticular) | matrix styrene-divinylbenzene (macroreticular) | matrix styrene-divinylbenzene (macroreticular) |
| 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 |
| 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 |
| separation technique reversed phase | separation technique reversed phase | separation technique reversed phase | separation technique reversed phase |
| technique(s) HPLC: suitable, LPLC: suitable | technique(s) HPLC: suitable, LPLC: suitable | technique(s) LPLC: suitable, solid phase extraction (SPE): suitable | technique(s) HPLC: suitable, LPLC: suitable |
Application
- Amberlite™ XAD®-2 was used as adsorbent in the extraction of organochlorine compounds using Soxhlat extraction technique.[1]
- Amberlite™ XAD®-2 was used as adsorbent in the extraction of honey samples using column chromatography for HPLC analysis.[2]
- Amberlite™ XAD®-2 was used in adsorption chromatography.[3]
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.
General description
Amberlite XAD-2, a hydrophobic copolymer of styrene-divinylbenzene resin, requires longer purification process and is commonly used as a sorbent.[4] Amberlite XAD-2 resin sorbs organic compounds depending upon the aromaticity and size of the hydrophobic groups through low-energy physical interactions.[5]
Nonionic macroreticular resin that adsorbs and releases ionic species through hydrophobic and polar interactions; usually used under isocratic conditions.
Specifications:
Specifications:
Legal Information
ASTM is a registered trademark of American Society for Testing and Materials
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Sorption of sodium dodecyl sulfate on amberlite XAD-2 resin.
HIRAIDE, Masataka, Toshihiko SHIMA, and Hiroshi KAWAGUCHI.
Analytical Sciences, 10, 505-507 (1994)
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
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
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
Claude Schummer et al.
Environmental pollution (Barking, Essex : 1987), 170, 88-94 (2012-07-10)
Passive air sampling has been shown to be a very interesting alternative to high-volume sampling by overcoming its disadvantages (size, weight, expensiveness). However, to date, only limited data is available about passive air sampling of current-use pesticides. In order to
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