Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

D3415

Sigma-Aldrich

Bisphenol A diglycidyl ether

viscous liquid, PPARγ inhibitor

Synonym(s):

BADGE, DGEBA, NSC 5022, 2,2-Bis[4-(glycidyloxy)phenyl]propane, 4,4′-Isopropylidenediphenol diglycidyl ether, D.E.R.™ 332

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C21H24O4
CAS Number:
1675-54-3
Molecular Weight:
340.41
Beilstein:
299026
EC Number:
216-823-5
MDL number:
MFCD00080480
UNSPSC Code:
12352200
PubChem Substance ID:
57654090
NACRES:
NA.77

product name

Bisphenol A diglycidyl ether,

form

viscous liquid

Quality Level

100

composition

Epoxide equivalent weight, 172-176

density

1.16 g/mL at 25 °C (lit.)

SMILES string

CC(C)(c1ccc(OCC2CO2)cc1)c3ccc(OCC4CO4)cc3

InChI

1S/C21H24O4/c1-21(2,15-3-7-17(8-4-15)22-11-19-13-24-19)16-5-9-18(10-6-16)23-12-20-14-25-20/h3-10,19-20H,11-14H2,1-2H3

InChI key

LCFVJGUPQDGYKZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Bisphenol A diglycidyl ether is an epoxy resin.

Application

Bisphenol A diglycidyl ether has been used:
  • to study its effects on propiomelanocortin (POMC):enhanced green fluorescent protein (EGFP) expression in our transgenic fish
  • to study the curing behavior, kinetics of epoxy, polyamidoamine systems and the influence of the incorporation of Fe3O4 magnetic nanoparticles (MNPs)
  • as a thermosetting resin
  • to determine the optimum composition of the epoxy-polysiloxane blend
  • for the preparation of transparent epoxy-based nanocomposite coatings
  • for the preparation, coating and curing of epoxy-graphene (E/G)

Biochem/physiol Actions

PPARγ inhibitor that blocks rosiglitazone- and insulin-induced adipogenesis.

Features and Benefits

This compound is featured on the Nuclear Receptors (PPARs) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Linkage

Epoxy resin often used in conjunction with DER 732 to form blocks of varying strength and hardness.

Legal Information

D.E.R. is a trademark of The Dow Chemical Company or an affiliated company of Dow

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H317,H319,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

507.2 - 514.4 °F - closed cup

Flash Point(C)

264 - 268 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enhanced Charpy impact strength of epoxy resin modified with vinyl-terminated polydimethylsiloxane
Vilcakova J, et al.
Journal of Applied Polymer Science, 135(4), 45720-45720 (2018)
Design and Manufacture of Textile Composites (2005)
Hoa H Le et al.
Endocrinology, 151(12), 5689-5699 (2010-10-12)
Estrogenic endocrine disrupting chemicals (EDCs) constitute a diverse group of man-made chemicals and natural compounds derived from plants and microbial metabolism. Estrogen-like actions are mediated via the nuclear hormone receptor activity of estrogen receptor (ER)α and ERβ and rapid regulation
Cure kinetics of epoxy/beta-cyclodextrin-functionalized Fe3O4 nanocomposites: experimental analysis, mathematical modeling, and molecular dynamics simulation
Saeb MR, et al.
Progress in Organic Coatings, 110, 172-181 (2017)
Calorimetric analysis and molecular dynamics simulation of cure kinetics of epoxy/chitosan-modified Fe3O4 nanocomposites
Saeb MR, et al.
Progress in Organic Coatings, 112, 176-186 (2017)
View All Related Papers

Protocols

Analysis of Bisphenol A and Analogous Compounds in Infant Formula

SupelMIP SPE-Bisphenol A gave high recovery for baseline resolution of five related compounds with LC-Fluorescence detection.

Analysis of Active Cannabis Compounds (Cannabinoids) in Edible Food Products: Gummy Bears and Brownies

Rapid potency testing of marijuana-infused edibles using LC/MS on a biphenyl stationary phase detected eleven cannabinoids.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service