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Merck
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Documenti

257591

Sigma-Aldrich

4,4′-(Hexafluoroisopropylidene)diphenol

97%

Sinonimo/i:

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

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About This Item

Formula condensata:
(CF3)2C(C6H4OH)2
Numero CAS:
1478-61-1
Peso molecolare:
336.23
Beilstein:
1891568
Numero CE:
216-036-7
Numero MDL:
MFCD00000439
Codice UNSPSC:
12162002
ID PubChem:
24855595
NACRES:
NA.23

Saggio

97%

Forma fisica

powder

Punto di fusione

160-163 °C (lit.)

Stringa SMILE

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
ZFVMWEVVKGLCIJ-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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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
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
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
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