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10952

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Araldite® M accelerator 960

accelerator DY 060

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UNSPSC Code:
41116121

Quality Level

refractive index

n/D 1.517

application(s)

hematology
histology

storage temp.

room temp

General description

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.

Application

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.

Legal Information

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

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Signal Word

Warning

Hazard Statements

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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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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)

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