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Merck
CN

13909-U

Amberchrom CG300

Amberchrom CG300M, 50-100 μm

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NACRES:
SB.52
UNSPSC Code:
23151817
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form

liquid

packaging

bottle of 100 mL

technique(s)

LPLC: suitable, thin layer chromatography (TLC): suitable

surface area

700 m2/g

matrix

styrene-divinylbenzene

matrix active group

polymer

particle size

50-100 μm

pore size

0.7 mL/g pore volume, 300 Å mean pore size

separation technique

reversed phase

General description

Amberchrom CG300 is macroporous polymeric adsorbent resin designed for use in capture and purification steps of downstream processing of synthetic oligonucleotides and polypeptides, such as insulin. It is the highest adsorbing resin for tumour necrosis factor-α (TNF-α), interleukin (IL-8) and C3a against charcoal as reference.

Application

用于快速吸附疏水性化合物的多环芳烃树脂,这些化合物包括:表面活性剂、中等分子量的蛋白质、多肽、较大的肽以及抗生素。可用于反相条件。
Amberchrom CG300 may be used in separation medium for TLC, paper chromatography and LPLC.

Legal Information

Amberchrom is a trademark of DuPont de Nemours, Inc.

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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C Tetta et al.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 13(6), 1458-1464 (1998-06-26)
Sepsis is associated with enhanced cytokine production. Here, we examined the in vitro removal of plasma cytokines during continuous plasmafiltration coupled with sorbent adsorption. Proinflammatory (tumour necrosis factor-alpha, interleukins-1, -8) and anti-inflammatory (interleukin 1 receptor antagonist, soluble tumour necrosis factor
Shuichi Yamamoto et al.
Journal of chromatography. A, 1162(1), 50-55 (2007-05-15)
A rational method for designing separation processes by chromatography with polystyrene-divinylbenzene (PS-DVB) resins of different particle diameters (10-400microm) was developed. As model samples, catechin and epigallocatehin gallate (EGCG) were chosen and the mobile phase was an ethanol-water mixture. Linear gradient

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