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NY1H00010

Millipore

Nylon Membrane Filter, 100.0 μm Pore Size

Millipore, 30 cm x 3 m, hydrophilic

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Synonym(s):
Nylon Net Filter
UNSPSC Code:
40161507
eCl@ss:
32031602
NACRES:
NB.24

material

Nylon membrane
plain filter
white filter

sterility

non-sterile

feature

hydrophilic

manufacturer/tradename

Millipore

parameter

100 °C max. temp. (curling may be seen at temperatures above 75°C)

filter L × W

30 cm × 3 m

thickness

80 μm

pore size

100.0 μm pore size
44 % porosity

shipped in

ambient

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General description

Filter Code: NY1H
Filter Type: Net filter
Nylon filters are compatible with a broad range of solvents. Two types are available: 1) Nylon Membrane Filters with pore sizes ranging from 0.20 to 1.2 µm, and 2) Woven Net Filters with mesh openings ranging from 5 to 180 µm.

Our 5 µm Nylon Woven Net Filter (NY054700) is commonly used in the automotive industry for cleanliness analysis.

Features & Benefits:
•Wide range of pore sizes available
•Resistant to aggressive solvents

Applications:
Particle Removal and Clarification; Solvent Filtration; Particle Analysis; Paint Monitoring; Automotive Cleanliness Analysis

Features and Benefits

  • Nylon filters display resistance to aggressive solvents.
  • Compatible with a broad range of solvents.
  • Applicable for use in solvent filtration, particle analysis, and clarification.


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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Yunlong Lu et al.
Frontiers in plant science, 6, 391-391 (2015-06-18)
The development of sperm cells (SCs) from microspores involves a set of finely regulated molecular and cellular events and the coordination of these events. The mechanisms underlying these events and their interconnections remain a major challenge. Systems analysis of genome-wide
Can Li et al.
STAR protocols, 1(3), 100195-100195 (2020-12-31)
Assessing IL-2-induced phosopho-STAT5 (pSTAT5) content can reveal the cytokine responsiveness of individual T cells. Identifying distinct T cell subsets by nuclear transcription factors, such as Foxp3, and concurrently quantifying intracellular pSTAT5, however, has been technically challenging. Conventional Foxp3 staining buffers quench pSTAT5
Artyom A Alekseyenko et al.
Current protocols in molecular biology, 109, 21-21 (2015-01-07)
In order to understand how chromatin complexes function in the nucleus, it is important to obtain a comprehensive picture of their protein, DNA, and RNA components, as well as their mutual interactions. This unit presents a chromatin cross-linking approach (BioTAP-XL)

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