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Safety Information

D6418

Sigma-Aldrich

DEAE-Cellulose

Fast Flow, fibers

Synonym(s):

Cellulose DEAE, Diethylaminoethyl-cellulose

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About This Item

CAS Number:
9013-34-7
MDL number:
MFCD00146622
UNSPSC Code:
47101511
PubChem Substance ID:
24894027

form

fibers

SMILES string

OC[C@@H]1O[C@@H](O[C@H]2[C@@H](O)[C@H](O)[C@@H](O)O[C@H]2CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3?,4?,5?,6?,7?,8?,9?,10-,11?,12+/m1/s1

InChI key

GUBGYTABKSRVRQ-WFVLMXAXSA-N

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Application

DEAE-Cellulose is used in ion exchange chromatography, protein chromatography and anion exchange media. DEAE cellulose has been used to study acute myocardial infarction.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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J Martin-Sanchez et al.
Experimental parasitology, 92(1), 57-63 (1999-05-18)
Isoenzyme electrophoresis and RAPD techniques were used to study the genetic polymorphism of different Spanish isolates of Theileria annulata in the schizont and piroplasm stages. Enzyme activity attributable to the parasite was detected in only 5 of the 13 loci
Buuan Lam et al.
Analytical chemistry, 78(24), 8194-8199 (2006-12-15)
A passive sampler for the isolation of dissolved organic matter (DOM) from freshwater environments is described. The sampler consists of a molecular weight selective membrane (1000 kDa) and an anion exchange resin (diethylaminoethylcellulose (DEAE-cellulose)). NMR indicates the samplers isolate DOM
Collagen-Induced Arthritis in Rats
Griffiths, M.M., et al.
Arthritis Research, 136(II), 201-214 (2007)
Xiang Ding et al.
International journal of biological macromolecules, 50(3), 613-618 (2012-01-31)
In this study, a novel heteropolysaccharide was isolated from the fruiting bodies of Boletus speciosus Forst through DEAE-cellulose column and Sephadex G-200 column. The Boletus speciosus Forst polysaccharide (BSFP-1) had a molecular weight of 1.33×10(4) Da and was mainly composed
Jana Stránská et al.
Biochimie, 89(1), 135-144 (2006-09-23)
A series of N,N'-bis(2-pyridinylmethyl)diamines was synthesized and characterized for their inhibition effects towards plant copper-containing amine oxidase (EC 1.4.3.6) and polyamine oxidase (EC 1.5.3.11), which mediate the catabolic regulation of cellular polyamines. Even though these enzymes catalyze related reactions and
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