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RAWP02500

Millipore

MCE Membrane Filter, 1.2 μm Pore Size

MF-Millipore™, filter diam. 25 mm, hydrophilic

Synonym(s):

MF-Millipore™ Membrane Filter, 1.2 µm pore size

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About This Item

UNSPSC Code:
40161507
eCl@ss:
32031602
NACRES:
NB.24

material

mixed cellulose esters (MCE) membrane
plain filter
white filter

Quality Level

400

Agency

in accordance with NIOSH 7400,7402
in accordance with OSHA ID 160

description

25 mm diameter, mixed cellulose esters (MCE) membrane, hydrophilic, white, 100 discs

sterility

non-sterile

feature

hydrophilic

manufacturer/tradename

MF-Millipore™
Millipore

parameter

20 L/min-cm2 air flow rate
270 mL/min-cm2 water flow rate
75 °C max. temp.

filter diam.

25 mm

thickness

150 μm

gravimetric extractables

5%

color

white

refractive index

n/D 1.512

matrix

MF-Millipore™

pore size

1.2 μm pore size
82 % porosity

bubble point

≥0.76 bar, air with water at 23 °C

shipped in

ambient

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General description

MF-Millipore™ membrane filters comprising biologically inert mixtures of cellulose acetate and cellulose nitrate have wide use in research and analytical applications.

Application

Clarification of aqueous solutions

Features and Benefits

  • For use in biological and environmental monitoring applications.
  • Autoclavable and compatible with ethylene oxide and gamma irradiation sterilization.

Legal Information

MF-Millipore is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Flame
GHS02

Signal Word

Danger

Hazard Statements

H228

Hazard Classifications

Flam. Sol. 1

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Werner Weitschies et al.
Journal of controlled release : official journal of the Controlled Release Society, 108(2-3), 375-385 (2005-10-11)
Gastrointestinal motility and transport as well as concomitant food intake are factors that are known to influence pharmacokinetics derived after intake of extended release dosage forms. However, the mechanisms behind these influencing factors are mostly unknown. In this study the
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PloS one, 8(5), e64419-e64419 (2013-05-16)
Construction of synthetic genetic networks requires the assembly of DNA fragments encoding functional biological parts in a defined order. Yet this may become a time-consuming procedure. To address this technical bottleneck, we have created a series of Gateway shuttle vectors

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