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470945

Sigma-Aldrich

Resorcinol diglycidyl ether

Synonym(s):

1,3-Bis(2,3-epoxypropoxy)benzene, 1,3-Diglycidyloxybenzene, Diglycidyl resorcinol ether, Resorcinol bis(2,3-epoxypropyl) ether, Resorcinol diglycidyl ether, Resorcinol glycidyl ether, m-Bis(2,3-epoxypropoxy)benzene

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About This Item

Empirical Formula (Hill Notation):
C12H14O4
CAS Number:
Molecular Weight:
222.24
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

form

solid

eq. wt.

120-135 Epoxide

refractive index

n20/D 1.542 (lit.)

viscosity

300-500 cP

bp

172 °C (lit.)

solubility

H2O: insoluble

density

1.21 g/mL at 25 °C (lit.)

SMILES string

C1OC1COc2cccc(OCC3CO3)c2

InChI

1S/C12H14O4/c1-2-9(13-5-11-7-15-11)4-10(3-1)14-6-12-8-16-12/h1-4,11-12H,5-8H2

InChI key

WPYCRFCQABTEKC-UHFFFAOYSA-N

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Application

Reactive diluent and modifier in epoxy resins used in coatings, potting and tooling compounds, adhesives and composites.

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

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, type P2 (EN 143) respirator cartridges


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J P Seiler
Chemico-biological interactions, 51(3), 347-356 (1984-10-01)
Aromatic diglycidyl compounds are very active mutagens when assayed in in vitro tests. In vivo, however, resorcinol diglycidyl ether provided no evidence for the clastogenic activity, while diglycidylaniline exhibited definite mutagenic activity in the micronucleus test. Since the only difference
Diglycidyl resorcinol ether.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 36, 181-188 (1985-02-01)
Diglycidyl resorcinol ether.
IARC monographs on the evaluation of carcinogenic risks to humans, 71 Pt 3, 1417-1420 (1999-09-07)
Sudhakar Godeshala et al.
Journal of materials chemistry. B, 8(37), 8558-8572 (2020-08-25)
Simultaneous delivery of small molecules and nucleic acids using a single vehicle can lead to novel combination treatments and multifunctional carriers for a variety of diseases. In this study, we report a novel library of aminoglycoside-derived lipopolymers nanoparticles (LPNs) for
Chaonan Huang et al.
Talanta, 190, 15-22 (2018-09-03)
This paper describes the poly(divinylbenzene) (PDVB) supported synthesis of quaternized hyperbranched macromolecules (QHMs) and its use as a highly selective, high-capacity mixed-mode anion-exchange (MAX) sorbent. In detail, the aminated PDVB support was firstly synthesized by copolymerization of divinylbenzene and 2-(diethylamino)ethyl

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