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Empore Extraction Disk solid phase extraction (SPE) Cartridge

matrix active group C18-SD, volume 3 mL, pk of 50

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About This Item

UNSPSC Code:
13111000
NACRES:
NB.21

product name

Empore Extraction Disk Cartridge, matrix active group C18-SD, volume 3 mL, pk of 50

material

polypropylene filter (graded density pre-filter)

feature

endcapped

packaging

pk of 50

manufacturer/tradename

CDS Analytical 98-0604-0198-5

extent of labeling

18% C loading

technique(s)

solid phase extraction (SPE): suitable

bed I.D.

7 mm

membrane thickness

0.75 mm

volume

3 mL

matrix active group

C18-SD

particle size

50 μm

pore size

60 Å pore size

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General description

Empore membrane SPE technology comprises of SPE particles tightly enmeshed within a network of inert PTFE fibrils (90% SPE particles : 10% PTFE, by weight). The SPE-membrane fabrication process results in a highly dense and uniform extraction medium that offers distinct advantages over traditional sorbent/packed-bed SPE products. Empore SPE technology provides a denser, more uniform extraction bed than traditional packed bed products allowing for smaller bed weights, shorter analyte to pore diffusion paths, and more efficient extractions.

Layed above the SPE membrane is a polypropylene pre-filter to prevent particulates from reaching the underlying membrane. The dense particle packing and uniform distribution within the Empore membane offers outsanding extraction efficiency and reproducibility.

Save Time & Money:
  • Reduced SPE Bed Mass = Reduced SPE Solvent & Elution Volumes
  • Minimize SPE eluate evaporation time
  • Potentially allows for direct injection of the SPE eluate
  • Dense & Uniform Extraction Medium = No SPE Channeling and Voiding
  • Efficient mass-transfer kinetics allow for faster flow rates
  • Eliminate SPE fines improving column and instrument life

Features and Benefits

  • Reduced sample and elution volumes
  • Reduced time for eluate evaporation
  • Increase sampling throughput
  • Eliminate channeling effects
  • High and reproducible recoveries

Other Notes

Recommended for the extraction of moderately-polar to non-polar analytes from aqueous samples (e.g., biological plasma).

Legal Information

Empore is a trademark of CDS Analytical

Disclaimer

CDS Analytical LLC recently acquired the rights to Empore products from 3M Purification Inc. For an interim phase, you may receive products packaged with either manfacturer′s branding.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Tianlan Lan et al.
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Major depressive disorder, as a destructive mental health disorder, is a major contributor to disability and death. Numerous studies have illustrated that activation of inflammation and fluctuating immune reactions play a crucial role in the physiopathology of depression. The effectiveness
Zehui Zhang et al.
FEBS letters, 593(8), 820-830 (2019-03-23)
The respiratory glycoprotein hemocyanin has been implicated in immune-related functions. Using lectin blotting, we show that the binding of shrimp (Litopenaeus vannamei) hemocyanin to concanavalin A decreases markedly with O-glycosidase treatment but not with PNGase F. Twelve O-glycosylation sites, three on
Yong He et al.
Life sciences, 211, 102-117 (2018-09-12)
Although decades of research have revealed numerous molecular abnormalities in the hippocampus associated with depression, the different mechanisms involved in the susceptibility and resilience of mice to chronic social defeat stress (CSDS)-induced depression remain poorly understand. Through the social defeat
Junlin Song et al.
BMC genomics, 20(1), 363-363 (2019-05-11)
Color polymorphism, a high-valued trait, is frequently observed in molluscan shellfish. The QN Orange scallop, a new scallop strain successively selected from the interspecific hybrids of the bay scallop (Argopecten irradians irradians) and the Peruvian scallop (Argopecten purpuratus), is distinguished
Changqing Du et al.
International journal of molecular medicine, 43(5), 1991-2004 (2019-03-22)
Acute myocardial infarction (AMI) is one of the most common and life‑threatening cardiovascular diseases. However, the ability to diagnose AMI within 3 h is currently lacking. The present study aimed to identify the differentially expressed proteins of AMI within 3

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