2,2'-Bis[4-(4-aminophenoxy)phenyl]propane, 98%

Name: 2,2'-Bis[4-(4-aminophenoxy)phenyl]propane, 98%
SKU: ACM13080869-1
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Catalog NumberACM13080869-1

CAS Number13080-86-9

CategoryMonomers

2,2'-Bis[4-(4-aminophenoxy)phenyl]propane, 98%

IUPAC Name

4-[4-[2-[4-(4-aminophenoxy)phenyl]propan-2-yl]phenoxy]aniline

Molecular Weight

410.5g/mol

Molecular Formula

C27H26N2O2

Canonical SMILES

CC(C)(C1=CC=C(C=C1)OC2=CC=C(C=C2)N)C3=CC=C(C=C3)OC4=CC=C(C=C4)N

InChI

InChI=1S/C27H26N2O2/c1-27(2,19-3-11-23(12-4-19)30-25-15-7-21(28)8-16-25)20-5-13-24(14-6-20)31-26-17-9-22(29)10-18-26/h3-18H,28-29H2,1-2H3

InChI Key

KMKWGXGSGPYISJ-UHFFFAOYSA-N

Application

2,2'-Bis[4-(4-aminophenoxy)phenyl]propane, 98%, serves as a versatile diamino monomer widely utilized in the development of advanced polymer materials. Its molecular structure, featuring two amine groups, allows it to effectively cross-link with carboxylic acids or carboxylic dianhydrides to synthesize high-performance polyimides. These polyimides find applications in innovative technologies such as batteries, fuel cells, low dielectric materials, and OLEDs, thanks to their unique characteristics, including a glass transition temperature around 225-230°C and notable thermoplastic-like behavior with distinct yield properties. Moreover, 2,2'-Bis[4-(4-aminophenoxy)phenyl]propane is instrumental in the curing of epoxy resins and the creation of poly(ε-caprolactone) blends, contributing to the formulation of crystalline thermoset materials. Additionally, its utility extends to the construction of dental resin composites, showcasing its broad applicability in various high-tech and industrial sectors.

Complexity

475

Covalently-Bonded Unit Count

EC Number

235-985-8

Exact Mass

410.199428g/mol

Formal Charge

Heavy Atom Count

Monoisotopic Mass

410.199428g/mol

Rotatable Bond Count