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452564

Sigma-Aldrich

Bisphenol A diacetate

98%

Synonym(s):

4,4′-Isopropylidenediphenol diacetate

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About This Item

Linear Formula:
(CH3CO2C6H4)2C(CH3)2
CAS Number:
10192-62-8
Molecular Weight:
312.36
EC Number:
233-472-3
MDL number:
MFCD00026194
UNSPSC Code:
12352100
PubChem Substance ID:
24868711
NACRES:
NA.22

Assay

98%

mp

91-94 °C (lit.)

SMILES string

CC(=O)Oc1ccc(cc1)C(C)(C)c2ccc(OC(C)=O)cc2

InChI

1S/C19H20O4/c1-13(20)22-17-9-5-15(6-10-17)19(3,4)16-7-11-18(12-8-16)23-14(2)21/h5-12H,1-4H3

InChI key

NSNHONPMCQYMNT-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

452564-25G:
452564-100G:
452564-VAR:
452564-BULK:

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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Model studies and a new melt polycondensation route to poly-bisphenol a-iso/terephthalate (polyarylate).
Oishi T and Hall HK.
Journal of Polymer Science Part A: Polymer Chemistry, 30(1), 83-89 (1992)
Migaku Kawaguchi et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 805(1), 41-48 (2004-04-29)
A new method, based on stir bar sorptive extraction (SBSE) with in situ derivatization and thermal desorption (TD)-gas chromatography-mass spectrometry (GC-MS) is described for the determination of trace amounts of bisphenol A (BPA) in river water, urine, plasma, and saliva
Motional heterogeneity and polymorphism of bisphenol-A diacetate.
Casarini D, et al.
Magnetic Resonance in Chemistry, 31(6), 540-547 (1993)
Bassam A Sweileh et al.
Molecules (Basel, Switzerland), 15(5), 3661-3682 (2010-07-27)
This work presents a new synthetic approach to aromatic and aliphatic polycarbonates by melt polycondensation of bisphenol A diacetates with alkylene- and arylenediphenyl dicarbonates. The diphenyl dicarbonates were prepared from phenyl chloroformate and the corresponding dihydroxy compounds. The process involved
Polycarbonate synthesis by the melt phase carbonate-ester interchange reaction of bisphenol-A diacetate with dimethyl carbonate.
Deshpande MM, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 33(4), 701-705 (1995)
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