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Safety Information

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:
25037-45-0
MDL number:
MFCD00084476
UNSPSC Code:
12162002
PubChem Substance ID:
24850948
NACRES:
NA.23

mol wt

average Mw ~45,000 by GPC

Quality Level

100

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

181625-BULK:
181625-500G:
181625-VAR:
181625-5G:
181625-250G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV6834
MKCW7195
MKCT9508
MKCS9502
MKCR5591

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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
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
A study on the effect of gamma radiation sterilization of polycarbonate (LMW).
M Jayabalan et al.
Biomedical sciences instrumentation, 23, 149-153 (1987-01-01)
Georgia P Tsintzou et al.
Journal of hazardous materials, 241-242, 137-145 (2012-10-10)
The various and widespread uses of polycarbonate (PC) polymers require a meaningful and environmentally friendly disposal method. In this study, depolymerisation of polycarbonate with water in a microwave reactor is suggested as a recycling method. Hydrolysis was investigated in an
R A Wind et al.
Solid state nuclear magnetic resonance, 1(2), 55-65 (1992-06-01)
We have investigated the EPR and DNP behavior of a molecularly doped polymer modeling those used to transport electronic charge in electrophotography. The EPR spectra show no evidence of the superexchange reported for a closely related system based on tri-p-tolylamine.
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