3-Hydroxybenzophenone, 98+%, Thermo Scientific Chemicals
3-Hydroxybenzophenone, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Hydroxybenzophenone, 98+%, Thermo Scientific Chemicals

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Quantity:
5 g
1 g
25 g
Catalog number A18061.06
also known as A18061-06
Price (USD)/ Each
176.00
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Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
176.00
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3-Hydroxybenzophenone, 98+%, Thermo Scientific Chemicals
Catalog numberA18061.06
Price (USD)/ Each
176.00
-
Add to cart
Chemical Identifiers
CAS13020-57-0
IUPAC Name3-benzoylphenol
Molecular FormulaC13H10O2
InChI KeySHULEACXTONYPS-UHFFFAOYSA-N
SMILESOC1=CC=CC(=C1)C(=O)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥98.5%
Melting Point (clear melt)113.0-119.0?C
Appearance (Color)Pale cream
FormPowder
3-Hydroxybenzophenone is a benzophenone metabolite with potential estrogenic and anti-androgenic activity. is a more attractive hydrogen bonding co-material for MCPBA, as the 3-hydroxyl group is unable to form an intramolecular hydrogen bond. It is commonly used as a radical and cationic photo initiators.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Hydroxybenzophenone is a benzophenone metabolite with potential estrogenic and anti-androgenic activity. is a more attractive hydrogen bonding co-material for MCPBA, as the 3-hydroxyl group is unable to form an intramolecular hydrogen bond. It is commonly used as a radical and cationic photo initiators.

Solubility
Soluble in Chloroform, DCM. Ethyl Acetate.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Yoko Kawamura.; Motoh Mutsuga.; Teruhisa Kato.; Mitsuru Iida.; Kenichi Tanamoto. strogenic and Anti-Androgenic Activities of Benzophenones in Human Estrogen and Androgen Receptor Mediated Mammalian Reporter Gene Assays.J. Health. Sci.,2005,51(48), 48-54.
  2. Marianne Placzek.; Markus Dendorfer.; Bernhard Przybilla.; Klaus-P. Gilbertz.; and Bernadette Eberlein. Photosensitizing Properties of Compounds Related to Benzophenone.Acta Derm Venereol.,2013,9330-32.