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257591

Sigma-Aldrich

4,4′-(Hexafluoroisopropylidene)diphenol

97%

Synonym(s):

2,2-Bis(4-hydroxyphenyl)hexafluoropropane, Bisphenol AF, Hexafluorobisphenol A

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About This Item

Linear Formula:
(CF3)2C(C6H4OH)2
CAS Number:
1478-61-1
Molecular Weight:
336.23
Beilstein/REAXYS Number:
1891568
EC Number:
216-036-7
MDL number:
MFCD00000439
UNSPSC Code:
12162002
PubChem Substance ID:
24855595
NACRES:
NA.23

Quality Level

100

assay

97%

form

powder

mp

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

InChI key

ZFVMWEVVKGLCIJ-UHFFFAOYSA-N

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Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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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Bisphenol F analytical standard

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Decafluorobiphenyl 99%

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Bisphenol A ≥99%

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Bisphenol A

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
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
Di Wu et al.
Chemosphere, 237, 124410-124410 (2019-07-31)
The profound influence of environmental chemicals on human health including inducing life-threatening gene mutation has been publicly recognized. Being a substitute for the extensively used endocrine-disrupting chemical BPA, Bisphenol AF (BPAF) has been known as teratogen with developmental toxicities and
Lalith Perera et al.
Toxicology in vitro : an international journal published in association with BIBRA, 44, 287-302 (2017-07-29)
Bisphenol A (BPA), bisphenol AF (BPAF), and bisphenol S (BPS) are well known endocrine disruptors. Previous in vitro studies showed that these compounds antagonize androgen receptor (AR) transcriptional activity; however, the mechanisms of action are unclear. In the present study
Miyu Nishikawa et al.
Applied microbiology and biotechnology, 102(2), 723-732 (2017-11-15)
Cytosolic sulfotransferases (SULTs), one of the predominant phase II drug metabolizing enzymes (DME), play important roles in metabolism of xeno- and endobiotics to generate their sulfo-conjugates. These sulfo-conjugates often have biological activities but are difficult to study, because even though
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