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257591

Sigma-Aldrich

4,4′-(Hexafluoroisopropylidene)diphenol

97%

Synonyme(s) :

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

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About This Item

Formule linéaire :
(CF3)2C(C6H4OH)2
Numéro CAS:
1478-61-1
Poids moléculaire :
336.23
Numéro Beilstein :
1891568
Numéro CE :
216-036-7
Numéro MDL:
MFCD00000439
Code UNSPSC :
12162002
ID de substance PubChem :
24855595
Nomenclature NACRES :
NA.23

Niveau de qualité

100

Pureté

97%

Forme

powder

Pf

160-163 °C (lit.)

Chaîne 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

Clé InChI

ZFVMWEVVKGLCIJ-UHFFFAOYSA-N

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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
STBK8453
STBJ7534
S34815
S34100
S29792

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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
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
Jie Zhang et al.
Toxicology letters, 283, 32-38 (2017-11-13)
The binding of bisphenol A (BPA) and its halogenated derivatives (halogenated BPAs) to mouse peroxisome proliferator-activated receptor α ligand binding domain (mPPARα-LBD) was examined by a combination of in vitro investigation and in silico simulation. Fluorescence polarization (FP) assay showed
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
Hiroyuki Okazaki et al.
Biological & pharmaceutical bulletin, 40(11), 1909-1916 (2017-11-03)
Bisphenols are endocrine disruptors that are widely found in the environment. Accumulating experimental evidence suggests an adverse interaction between bisphenols and estrogen signaling. Most studies have performed experiments that focused on estrogen receptor (ER) engagement by bisphenols. Therefore, the effects
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