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257591

Sigma-Aldrich

4,4′-(Hexafluoroisopropylidene)diphenol

97%

Sinônimo(s):

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

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About This Item

Fórmula linear:
(CF3)2C(C6H4OH)2
Número CAS:
1478-61-1
Peso molecular:
336.23
Beilstein:
1891568
Número CE:
216-036-7
Número MDL:
MFCD00000439
Código UNSPSC:
12162002
ID de substância PubChem:
24855595
NACRES:
NA.23

Nível de qualidade

100

Ensaio

97%

forma

powder

pf

160-163 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

ZFVMWEVVKGLCIJ-UHFFFAOYSA-N

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Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
STBJ7534
S34815
S34100
S29792
S28138

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Bis(4-fluorophenyl) sulfone 99%

Sigma-Aldrich

F15145

Bis(4-fluorophenyl) sulfone

Bisphenol E analytical standard

Supelco

04487

Bisphenol E

4,4′-(Hexafluoroisopropylidene)diphthalic anhydride 99%

Sigma-Aldrich

386448

4,4′-(Hexafluoroisopropylidene)diphthalic anhydride

Bisphenol S analytical standard

Supelco

43034

Bisphenol S

Bisphenol F analytical standard

Supelco

51453

Bisphenol F

Decafluorobiphenyl 99%

Sigma-Aldrich

D227

Decafluorobiphenyl

Bisphenol A ≥99%

Supelco

239658

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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