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08138

Supelco

Bisphenol BP

analytical standard

Synonyme(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

Formule empirique (notation de Hill):
C25H20O2
Numéro CAS:
1844-01-5
Poids moléculaire :
352.43
Numéro Beilstein :
2059947
Numéro MDL:
MFCD00045785
Code UNSPSC :
85151701
ID de substance PubChem :
329748555
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥98.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Application(s)

cleaning products
cosmetics
food and beverages
personal care

Format

neat

Chaîne SMILES 

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

Clé InChI

BATCUENAARTUKW-UHFFFAOYSA-N

Description générale

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).

Produits recommandés

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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335,H413

Classification des risques

Aquatic Chronic 4 - 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 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
BCCH4952
BCCB9937
BCBV7304
BCBN6793V
BCBN6793

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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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