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Araldite® M Beschleuniger 960

accelerator DY 060

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About This Item

UNSPSC-Code:
41116121

Qualitätsniveau

100

Brechungsindex

n/D 1.517

Anwendung(en)

hematology
histology

Lagertemp.

room temp

Allgemeine Beschreibung

Araldite is an epoxy resin commonly used for embedding. It is basically free from polymerization damage and the plastic does not sublime in the microscope, hence providing continual support and preservation of fine detail. It is composed of araldite M or CY 212, dodecenyl succinic anhydride, dibutyl phthalate and 2,4,6-tridimethylamine methyl phenol.

Anwendung

Araldite® was used to study electrochemical detection of dopamine and ascorbic acid neurotransmitters focusing on miniaturization of a graphite-epoxy and synthetic zeolite-modified graphite-epoxy composite macroelectrode as a quasi-microelectrode. It was also used in production of microfluidic chips using extremely low cost chemicals and equipment which was validated by producing monodisperse polymeric microparticles for drug delivery and hydrogel microfibers for cell embedding.

Rechtliche Hinweise

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

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Analysenzertifikate (COA)

Lot/Batch Number
BCBW2569
BCBH8004V
BCBG0630V
1378654
1362273

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Die Dokumentenbibliothek aufrufen

Simultaneous/selective detection of dopamine and ascorbic acid at synthetic zeolite-modified/graphite-epoxy composite macro/quasi-microelectrodes.
Ilinoiu EC
Sensors, 13 (6), 7296-7307 (2013)
S Focaroli et al.
Lab on a chip, 14(20), 4007-4016 (2014-08-22)
The present paper describes the production of microfluidic chips using an approach based on shrinkable biocompatible polymers (i.e. agarose) for the production of size controlled microfluidic channels. In addition, all steps of chip production were carried out using an inexpensive
Astrid M Parsons et al.
Dalton transactions (Cambridge, England : 2003), 48(29), 10945-10952 (2019-06-06)
The active fragment [Tp'Rh(CNneopentyl)], generated from the precursor Tp'Rh(CNneopentyl)(PhN[double bond, length as m-dash]CNneopentyl), underwent oxidative addition of substituted ketones and esters resulting in Tp'Rh(CNneopentyl)(R)(H) complexes (Tp' = tris-(3,5-dimethylpyrazolyl)borate). These C-H activated complexes underwent reductive elimination at varying temperatures (24-70 °C)
In Situ Hybridization in Electron Microscopy.
Morel G
Science, 174-175 (2001)
Biological Techniques.
Yadav P.R.
Science, 79-80 (2006)

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