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11048-U

Supelco

Carboxen® Carbon Adsorbent

matrix Carboxen® 569, 20-45 mesh, bottle of 500 g

Synonym(s):

carbon adsorbent, CMS, 60-80 mesh

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About This Item

EC Number:
231-153-3
UNSPSC Code:
23201100
NACRES:
SB.54

product name

Carboxen® Adsorbent, matrix Carboxen® 569, 20-45 mesh, bottle of 500 g

product line

Carboxen®

Quality Level

100

form

powder

packaging

bottle of 500 g

technique(s)

LPLC: suitable

surface area

~485 m2/g

matrix

Carboxen® 569

matrix active group

carbon

particle size

20-45 mesh

pore size

~0.10 cm3/g macroporosity
~0.14 cm3/g mesoporosity
~0.20 cm3/g microporosity
~5-8 Å pore diameter

density

~0.61 g/mL (free fall density)

separation technique

reversed phase

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General description

Carboxen® Adsorbent is ideally used for solid-phase microextraction (SPME). It is highly efficient in extraction of small polar molecules from aqueous solution.
Carboxens are a highly engineered synthetic carbon adsorbent engineered from polymeric precursors. These particles will not plastically deform like resins or generate fines like activated carbon. These materials are shipped and stored dried. These derivatized resins bring value to a wide range of purification applications for removing both small and large molecule impurities. They find use in both gas and liquid phase purifications. Some examples include removal of homogenous catalysts from active pharmaceutical ingredients (API)s, high-risk impurities in biochemical purifications such as host cell proteins from mAbs, removal of toxic heavy metals, purification of chlorinated molecules, and removal of extractables and leachables. Tapered pores result in increased thermodynamic and kinetic properties for both adsorption and desorption. The Carboxens vary in the relative percentage of pore structures (micro, meso, and macro), surface area, and surface pH.

Application

Carboxen® 569 was used for trapping a range of replacement chlorofluorocarbons varying in boiling point from -48.4 to -9.8°C which is highly advantageous for analysis of trace gases in atmosphere.

Features and Benefits

Features and Benefits:

  • Spherical
  • Hard (ball pan hardness >98%)
  • Stable up to 400°C
  • High purity
  • Easy to pack
  • Stable over entire pH range
  • Do not create backpressure
  • High osmotic shock stability
  • Tapered pore sizing (from macro- to meso- to micro-)

Other Notes

For more information, please visit: specialty Carbon Adsorbents

Legal Information

Carboxen is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Evaluation of Carboxen carbon molecular sieves for trapping replacement chlorofluorocarbons.
O'Doherty SJ, et al.
Journal of Chromatography A, 630 (1), 265-274 (1993)
B D Page et al.
Journal of chromatography. A, 873(1), 79-94 (2000-04-11)
The headspace solid-phase microextraction (HS-SPME) efficiencies from vegetable oil of the recently available Carboxen-poly(dimethylsiloxane) (PDMS) and divinylbenzene-Carboxen-PDMS fibres were found to be much greater than those of the PDMS fibre for a number of volatile contaminants. Using these Carboxen-based fibres
Dawn M Chapman et al.
Journal of agricultural and food chemistry, 52(17), 5431-5435 (2004-08-19)
A rapid and automated solid phase microextraction (SPME) stable isotope dilution gas chromatography/mass spectrometry (GC-MS) method for 2-methoxy-3-isobutylpyrazine (MIBP) quantification in red wine was developed. Wines with 30% (w/v) NaCl and 2-methoxy-(2)H(3)-3-isobutylpyrazine internal standard were sampled with a 2 cm
Sebastien Allard et al.
Journal of chromatography. A, 1238, 15-21 (2012-04-13)
Trihalomethanes are predominantly formed during disinfection of water via reactions of the oxidant with natural organic matter. Even though chlorinated and brominated trihalomethanes are the most widespread organic contaminants in drinking water, when iodide is present in raw water iodinated
Lucia Giordano et al.
Journal of chromatography. A, 1017(1-2), 141-149 (2003-10-31)
A new method was developed for the determination of 2-furfural (2-F) and 5-methylfurfural (5-MF), two products of Maillard reaction in vinegar, with head-space solid-phase microextraction (HS-SPME) coupled to gas chromatography-mass spectrometry (GC-MS). A divinylbenzene (DVB)/carboxen (CAR)/polydimethylsiloxane (PDMS) fibre was used
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