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181625

Sigma-Aldrich

Poly(Bisphenol A carbonate)

average Mw ~45,000 by GPC

Synonym(s):

4,4′-Dihydroxydiphenyl-2,2-propane carbonate polymer, Bisphenol A carbonate homopolymer, Carbonic acid-4,4′-dihydroxydiphenyl-2,2-propane copolymer, Poly(dian carbonate), Poly[2,2-bis(4-hydroxyphenyl)propane carbonate]

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

mol wt

average Mw ~45,000 by GPC

Quality Level

refractive index

n20/D 1.585

transition temp

Tg 150 °C
Tm 267 °C

density

1.2 g/mL at 25 °C (lit.)

SMILES string

CC(C)(c1ccc(O)cc1)c2ccc(O)cc2

InChI

1S/C15H16O2.CH2O3/c1-15(2,11-3-7-13(16)8-4-11)12-5-9-14(17)10-6-12;2-1(3)4/h3-10,16-17H,1-2H3;(H2,2,3,4)

InChI key

XSXWYGABGYBZRM-UHFFFAOYSA-N

Gene Information

mouse ... Esr1(13982)
rat ... Ar(24208)

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General description

Poly(Bisphenol A carbonate) (PC) is a thermoplastic polymer with optical clarity, high refractive index, and toughness. It can be used to prepare optical lenses and as a supporting matrix to fabricate hybrid nanofiber membranes.

Application

Poly(Bisphenol A carbonate) has been used:
  • To prepare transparent nanocomposites for optical applications.
  • To study the wettability of graphene.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Hiroshi Yabu et al.
Langmuir : the ACS journal of surfaces and colloids, 22(11), 4992-4997 (2006-05-17)
We describe here a preparation of pincushion structures with holes, hexagonally arranged microrings, and microdots by simple heating and peeling of self-organized honeycomb-patterned films. We have reported that the honeycomb-patterned films can be prepared by casting the solution of an
Yuki Kitahara et al.
Chemosphere, 80(11), 1281-1284 (2010-07-16)
The thermal decomposition of poly(bisphenol A carbonate) (PoC) results in the formation of the endocrine disruptor bisphenol A (BPA). In the present work, we investigated the kinetics of the thermal decomposition of PoC, and the subsequent decomposition of BPA, under
Molla R Islam et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(22), 6098-6108 (2011-04-19)
Spontaneous phase-separated, controlled aggregate structures of photo- and electroactive molecules in polymer matrices are of interest for device fabrication. We show that the self-assembly of octabutoxyphthalocyanine (Pc) in polymer matrices leads to tubular morphology of Pc when the film is
Vianney Souplet et al.
Methods in molecular biology (Clifton, N.J.), 570, 287-297 (2009-08-04)
Microarrays are frequently prepared on microscope glass slides. However, glass substrates can break or cut and thus can lead to the contamination of the manipulator during the analysis of biological samples. Alternately, bisphenol A polycarbonate (PC) is shock-resistant and, in
L Coulier et al.
Journal of chromatography. A, 1070(1-2), 79-87 (2005-05-03)
Size exclusion chromatography (SEC), gradient polymer elution chromatography (GPEC) and liquid chromatography at critical conditions (LC-CC) have been developed and applied to observe chemical changes in poly(bisphenol A)carbonate (PC) due to hydrolytic degradation. Especially LC-CC appeared to be very successful

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