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Sigma-Aldrich

4,4′-(Hexafluorisopropyliden)diphenol

97%

Synonym(e):

2,2-Bis-(4-hydroxyphenyl)-hexafluorpropan, Hexafluorbisphenol A

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About This Item

Lineare Formel:
(CF3)2C(C6H4OH)2
CAS-Nummer:
1478-61-1
Molekulargewicht:
336.23
Beilstein:
1891568
EG-Nummer:
216-036-7
MDL-Nummer:
MFCD00000439
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24855595
NACRES:
NA.23

Assay

97%

Form

powder

mp (Schmelzpunkt)

160-163 °C (lit.)

SMILES String

Oc1ccc(cc1)C(c2ccc(O)cc2)(C(F)(F)F)C(F)(F)F

InChI

1S/C15H10F6O2/c16-14(17,18)13(15(19,20)21,9-1-5-11(22)6-2-9)10-3-7-12(23)8-4-10/h1-8,22-23H

InChIKey

ZFVMWEVVKGLCIJ-UHFFFAOYSA-N

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Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Tengfei Wang et al.
Talanta, 178, 481-490 (2017-11-16)
Using sulfonated and fluorinated poly (arylene ether ketone) comprising functional strong coordination group benzimidazole (SPAEK-F-BI) as a template film, a novel fabrication method of cobalt nanoflowers (CoNFs) and non-enzymatic glucose electrochemical sensor was developed in this work. After the precursors
Tara R Catron et al.
Toxicological sciences : an official journal of the Society of Toxicology, 167(2), 468-483 (2018-10-16)
Host-associated microbiota can biotransform xenobiotics, mediate health effects of chemical exposure, and play important roles in early development. Bisphenol A (BPA) is a widespread environmental chemical that has been associated with adverse endocrine and neurodevelopmental effects, some of which may
John Moreman et al.
Environmental science & technology, 51(21), 12796-12805 (2017-10-11)
Bisphenol A (BPA), a chemical incorporated into plastics and resins, has estrogenic activity and is associated with adverse health effects in humans and wildlife. Similarly structured BPA analogues are widely used but far less is known about their potential toxicity
Caroline Pinto et al.
Toxicology and applied pharmacology, 380, 114709-114709 (2019-08-16)
The high volume production compound bisphenol A (BPA) is of environmental concern largely because of its estrogenic activity. Consequently, BPA analogues have been synthesized to be considered as replacement molecules for BPA. These analogues need to be thoroughly evaluated for
A Jurek et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(7), 1225-1238 (2017-04-13)
Bisphenol A (BPA; 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol), a suspected endocrine disruptor with a weak estrogenic activity, is used in a variety of consumer products, including food-contact materials made of paper and cardboard products. Due to restrictions on the use of BPA because of
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