4,4′-Cyclohexylidenebisphenol

Name: 4,4′-Cyclohexylidenebisphenol
Brand: ALDRICH
Price: 59.6 CHF

98%

Sinonimo/i:

Bisphenol Z

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25 G

CHF 59.60

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Informazioni su questo articolo

Formula condensata:

C₆H₁₀(C₆H₄OH)₂

Numero CAS:

843-55-0

Peso molecolare:

268.35

NACRES:

NA.23

PubChem Substance ID:

24868244

UNSPSC Code:

12162002

EC Number:

212-677-1

MDL number:

MFCD00019341

Documenti fondamentali

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InChI key

SDDLEVPIDBLVHC-UHFFFAOYSA-N

InChI

1S/C18H20O2/c19-16-8-4-14(5-9-16)18(12-2-1-3-13-18)15-6-10-17(20)11-7-15/h4-11,19-20H,1-3,12-13H2

SMILES string

Oc1ccc(cc1)C2(CCCCC2)c3ccc(O)cc3

assay

98%

mp

190-192 °C (lit.)

Categorie correlate

Biomedical Materials

Monomers

Polymerization Tools

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1 of 4

Questo articolo	450464	450456	450502
Sigma-Aldrich 450421 4,4′-Cyclohexylidenebisphenol	Sigma-Aldrich 450464 4,4′-(1,3-Phenylenediisopropylidene)bisphenol	Sigma-Aldrich 450456 4,4′-(1-Phenylethylidene)bisphenol	Sigma-Aldrich 450502 4,4′-Isopropylidenebis(2,6-dimethylphenol)
assay 98%	assay 99%	assay 99%	assay 98%
mp 190-192 °C (lit.)	mp 135-139 °C (lit.)	mp 188-191 °C (lit.)	mp 162-165 °C (lit.)

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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A comparison of electrospray ionization, atmospheric pressure chemical ionization, and atmospheric pressure photoionization for the liquid chromatography/tandem mass spectrometric analysis of bisphenols. Application to bisphenols in thermal paper receipts and U.S. currency notes.

Henry J Eichman et al.

Rapid communications in mass spectrometry : RCM, 31(20), 1773-1778 (2017-08-03)

Human health concerns have arisen for common bisphenols (BPA and BPS) as well as new structural analogs. While native sulfone bisphenols and sulfone-derivatized bisphenols are amenable to electrospray ionization (ESI), alternative ionization methods such as atmospheric pressure chemical ionization (APCI)

Biotransformation of bisphenol A analogues by the biphenyl-degrading bacterium Cupriavidusbasilensis - a structure-biotransformation relationship.

Marie-Katherin Zühlke et al.

Applied microbiology and biotechnology, 104(8), 3569-3583 (2020-03-04)

Comparative analyses determined the relationship between the structure of bisphenol A (BPA) as well as of seven bisphenol analogues (bisphenol B (BPB), bisphenol C (BPC), bisphenol E (BPE), bisphenol F (BPF), bisphenol Z (BPZ), bisphenol AP (BPAP), bisphenol PH (BPPH))

Urinary bisphenol analogues and triclosan in children from south China and implications for human exposure.

Yi Chen et al.

Environmental pollution (Barking, Essex : 1987), 238, 299-305 (2018-03-25)

Bisphenols and triclosan (TCS) are widely used in consumer products. However, knowledge on human exposure to these anthropogenic chemicals has remained limited in China, especially for children. In this study, concentrations of seven bisphenols and TCS were determined in 283

Non-targeted screening of plastic-related chemicals in food collected in Montreal, Canada.

Lei Tian et al.

Food chemistry, 326, 126942-126942 (2020-05-15)

A non-targeted screening method based on ultrasound-assisted extraction followed by high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (HPLC-QTOF-MS) was developed to screen for the presence of plastic-related chemicals (PRCs) in different types of food (fish, chicken, canned tuna

Electron ionization induced fragmentation of fluorinated derivatives of bisphenols.

Magda Caban et al.

Rapid communications in mass spectrometry : RCM, 34(19), e8860-e8860 (2020-06-14)

Fluorinated derivatization agents allow for the identification and quantification of emerging pollutants with high sensitivity, yet details of their potential applications using electron ionization are lacking. The fluorine atom itself does not effectively participate in electron ionization. Furthermore, limited information

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4,4′-Cyclohexylidenebisphenol