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08138

Supelco

Bisphenol BP

analytical standard

Synonym(s):

1,1-Bis(4-hydroxyphenyl)-1,1-diphenylmethane, 4,4′-(Diphenylmethylene)diphenol, 4,4′-Dihydroxytetraphenylmethane, Bis(4-hydroxyphenyl)diphenylmethane, NSC 30848

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About This Item

Empirical Formula (Hill Notation):
C25H20O2
CAS Number:
Molecular Weight:
352.43
Beilstein:
2059947
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

SMILES string

OC(C=C1)=CC=C1C(C2=CC=C(O)C=C2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

1S/C25H20O2/c26-23-15-11-21(12-16-23)25(19-7-3-1-4-8-19,20-9-5-2-6-10-20)22-13-17-24(27)18-14-22/h1-18,26-27H

InChI key

BATCUENAARTUKW-UHFFFAOYSA-N

General description

Bisphenol BP belongs to the class of bisphenols.

Application

Bisphenol BP may be used as a reference standard in the determination of bisphenol BP in serum samples using high performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS).

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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A New Generation Material Graphene: Applications in Water Technology (2018)
Determination of trace levels of eleven bisphenol A analogues in human blood serum by high performance liquid chromatography-tandem mass spectrometry.
Owczarek K, et al.
The Science of the Total Environment, 628, 1362-1368 (2018)
Karolina Czarny et al.
Chemosphere, 263, 128299-128299 (2020-12-11)
In the last decades, the use of bisphenol A has attracted global attention resulting from its actions as an endocrine disrupting compound. In this regard, various bisphenol analogues have been manufactured as a replacement for this compound in consumer products.

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