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A9960

Sigma-Aldrich

Amberlite IRA-67 free base

gel form, 16-50 mesh (wet)

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Synonym(s):
1,2-bis(ethenyl)benzene,4-[(E)-2-[(E)-2-but-3-enoxyethenoxy]ethenoxy]but-1-ene,N-[3-(dimethylamino)propyl]prop-2-enamide
CAS Number:
MDL number:
NACRES:
NA.56

form

gel form

Quality Level

contains

~60% moisture content

parameter

≤60 °C temperature

moisture

~60%

matrix

Acrylic (gel)

matrix active group

polyamine

particle size

16-50 mesh (wet)

pH

0-7(effective)

capacity

1.6 meq/mL
5.6 meq/g

InChI

1S/C12H18O3.C10H10.C8H16N2O/c1-3-5-7-13-9-11-15-12-10-14-8-6-4-2;1-3-9-7-5-6-8-10(9)4-2;1-4-8(11)9-6-5-7-10(2)3/h3-4,9-12H,1-2,5-8H2;3-8H,1-2H2;4H,1,5-7H2,2-3H3,(H,9,11)/b11-9+,12-10+;;

InChI key

ZGXNLYRRYYOMNG-JDDKLYJPSA-N

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Application

Amberlite IRA-67 free base can be used in anion exchange media. It has been used as an adsorbent for lactic acid extraction from aqueous solution, and for the extraction of rhinacanthin from Rhinacanthus nasutus leaves.
Weakly basic anion exchange resin with an unusually high capacity for large organics. Common applications include: deacidification, deionization of process liquors, isolation of acidic natural products, purification of novabiacin and cephalosporins, separation of neutral and acidic amino acids below pH 10, removal of heparinic acid at low pH, concentration of citric acid, and demineralization of cheese whey.

Other Notes

Previously known as IRA-68.

Legal Information

Amberlite is a trademark of DuPont de Nemours, Inc.

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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P Gluszcz et al.
Bioprocess and biosystems engineering, 26(3), 185-190 (2004-03-05)
The aim of the study was to determine properties of selected ion-exchange resins for citric and lactic acids recovery, to define sorption isotherms for these acids at different temperatures (in the range of 20-60 degrees C) and to determine diffusion
The role of lactic acid adsorption by ion exchange chromatography.
Gao, Q., et al.
PLoS ONE, 5, 13948-13948 (2010)
P Panichayupakaranant et al.
Journal of chromatographic science, 47(8), 705-708 (2009-09-24)
A reversed-phase high-performance liquid chromatographic method is described for the simultaneous determination of rhinacanthin-C, rhinacanthin-D, and rhinacanthin-N in Rhinacanthus nasutus leaves. The method involved the use of a TSK-gel ODS-80Ts column (5 microm, 4.6 x 150 mm i.d.) with the

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