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10952

Sigma-Aldrich

Araldite® M accelerator 960

accelerator DY 060

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Codice UNSPSC:
41116121

Livello qualitativo

Indice di rifrazione

n/D 1.517

applicazioni

hematology
histology

Temperatura di conservazione

room temp

Descrizione generale

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.[1] It is composed of araldite M or CY 212, dodecenyl succinic anhydride, dibutyl phthalate and 2,4,6-tridimethylamine methyl phenol.[2]

Applicazioni

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.[3] 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.[4]

Note legali

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

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Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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


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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)
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)
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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