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08138

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Bisphenol BP

analytical standard

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

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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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
A New Generation Material Graphene: Applications in Water Technology (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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