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15138

Supelco

Bisphenol A diglycidyl ether

analytical standard

Synonym(s):

2,2-Bis[4-(glycidyloxy)phenyl]propane, 4,4′-Isopropylidenediphenol diglycidyl ether, BADGE, D.E.R. 332

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About This Item

Empirical Formula (Hill Notation):
C21H24O4
CAS Number:
Molecular Weight:
340.41
Beilstein:
299026
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

40-47 °C

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CC(C)(c1ccc(OCC2CO2)cc1)c3ccc(OCC4CO4)cc3

InChI

1S/C21H24O4/c1-21(2,15-3-7-17(8-4-15)22-11-19-13-24-19)16-5-9-18(10-6-16)23-12-20-14-25-20/h3-10,19-20H,11-14H2,1-2H3

InChI key

LCFVJGUPQDGYKZ-UHFFFAOYSA-N

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Ion Mobility: TWCCSN2 value of 195.6 Å2 [M+H]+ and 174.5 Å2 [M+Na]+

The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.

TWCCS measurements are expected to be within 2% of this reference value.

P/N 15138 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.
Standard for determining toxic monomers released from polymers of the inner coating of cans.

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.

Legal Information

D.E.R. is a trademark of The Dow Chemical Company or an affiliated company of Dow

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

507.2 - 514.4 °F - closed cup

Flash Point(C)

264 - 268 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Chromatographia, 34, 67-67 (1992)
Alexandros G Asimakopoulos et al.
Journal of chromatography. A, 1324, 141-148 (2013-12-10)
A liquid-liquid extraction (LLE; ethyl acetate) protocol, followed by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) methodology, was developed for the determination of 19 compounds, including bisphenol A diglycidyl ethers (BADGEs; industrial ethers), benzophenone-type UV filters (BP-UV filters; precursors and
Natchanun Leepipatpiboon et al.
Journal of chromatography. A, 1073(1-2), 331-339 (2005-05-25)
A gradient reversed-phase liquid chromatography with fluorescence detection method for simultaneous identification and quantification of bisphenol-A-diglycidyl ether (BADGE), bisphenol-F-diglycidyl ether (BFDGE), and their 10 derivatives in food matrixes was developed and validated for the analysis of oil-in-water- and aqueous-based foodstuffs.
K Celinski et al.
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 62(3), 347-356 (2011-09-07)
Recent studies indicate the involvement of peroxisone proliferator-activated receptor-γ (PPAR-γ) in the inflammatory reaction. The exact mechanism of PPAR-γ action has not been elucidated. It is supposed that PPAR-γ regulates transcription of genes responsible for encoding cytokines involved in the
Raquel Chamorro-García et al.
Environmental health perspectives, 120(7), 984-989 (2012-07-06)
Bisphenol A (BPA) and bisphenol A diglycidyl ether (BADGE), used in manufacturing coatings and resins, leach from packaging materials into food. Numerous studies suggested that BPA and BADGE may have adverse effects on human health, including the possibility that exposure

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