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Merck
CN

430234

Bisphenol A diglycidyl ether, brominated

mol wt 350-450 g/epoxide by perchloric acid method

Synonym(s):

4,4′-(1-Methylethylidene)bis[2,6-dibromophenol] polymer with (chloromethyl)oxirane, 4,4′-(1-methylethylidene)bis(2,6-dibromophenol), Tetrabromobisphenol A-epichlorohydrin polymer

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About This Item

CAS Number:
40039-93-8
UNSPSC Code:
12162002
NACRES:
NA.23
MDL number:
MFCD03703563

Key Documents

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Product Name

Bisphenol A diglycidyl ether, brominated, mol wt 350-450 g/epoxide by perchloric acid method

SMILES string

Brc2c(c(cc(c2)C(C)(C)c3cc(c(c(c3)Br)O)Br)Br)O.ClCC1OC1

InChI

1S/C15H12Br4O2.C3H5ClO/c1-15(2,7-3-9(16)13(20)10(17)4-7)8-5-11(18)14(21)12(19)6-8;4-1-3-2-5-3/h3-6,20-21H,1-2H3;3H,1-2H2

InChI key

DEGGCMXJUHYWMD-UHFFFAOYSA-N

form

solid

mol wt

350-450 g/epoxide by perchloric acid method

extent of labeling

48 wt. % Br

viscosity

1,800 cSt(lit.)

mp

55-65 °C (lit.)

transition temp

softening point 55-65 °C (Durrans)

solubility

a variety of ketone, aromatic hydrocarbon and ether alcohol solvents: soluble

Quality Level

100

Related Categories

Application

Imparts flame retardancy to molding, laminating and casting systems.

General description

A non-sintering material, high bromine content, low softening point.
Bisphenol A diglycidyl ether, brominated is a brominated epoxy resin that is used as a flame retardant material. It is majorly utilized as a combustible epoxy resin in the production of electronic printed boards.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317,H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW9355
MKCQ8198
MKCF7155
MKBX9424V
MKBN9812V

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E Kirschning et al.
Journal of neuroscience research, 53(4), 465-474 (1998-08-26)
Galactocerebroside (GalC) and sulfatide are major constituent lipids in vertebrate myelin. Their precise immunolocalization in electron microscopy so far has been hampered by the fact that lipids are not immobilized by chemical fixation and thus get extracted during dehydration with
A G Pogorelov et al.
Bulletin of experimental biology and medicine, 141(4), 513-519 (2006-12-13)
Electron probe microanalysis is a method for evaluation of concentrations of elements at the subcellular level, effective in studies of an individual cell in culture or suspension. Intracellular concentrations of cytoplasmic ions (K+, Na+, Cl-) most rapidly and markedly reacting
J C Stockert et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 52(5-6), 408-411 (1997-05-01)
Treatment of chicken blood smears and semithin sections from Epon-embedded mouse tissues with aqueous solutions of the 3-aminonaphthalimides FA-142, FA-2043, and FA-2143 induced a strong green-yellow fluorescence of chromatin under violet or violet-blue excitation. Chromatin emission was abolished by previous
I Cavusoglu et al.
European journal of morphology, 39(5), 313-317 (2002-09-11)
Successful results of microwave polymerisation of different epoxy formulations have been reported in the literature. The present study was intended to shorten the time needed for polymerisation of epoxy resin by the use of a microwave technique. A standard double
C M Ayanoglou et al.
Journal of periodontal research, 32(7), 614-618 (1997-12-24)
The aim of the present investigation was to examine if new cementum (NC) formed during cyclosporin A (CsA) administration was maintained after suspension of the treatment. Thirty mg/kg/d of CsA were given to 3 male Sprague-Dawley rats. Three control rats
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