452564
Bisphenol A diacetate
98%
Sinónimos:
4,4′-Isopropylidenediphenol diacetate
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About This Item
Fórmula lineal:
(CH3CO2C6H4)2C(CH3)2
Número de CAS:
Peso molecular:
312.36
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
98%
mp
91-94 °C (lit.)
functional group
ester
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
Categorías relacionadas
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
Motional heterogeneity and polymorphism of bisphenol-A diacetate.
Casarini D, et al.
Magnetic Resonance in Chemistry, 31(6), 540-547 (1993)
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
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)
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
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