4-(4-Hydroxyphenyl)-2-butanone, 98%, Thermo Scientific Chemicals
4-(4-Hydroxyphenyl)-2-butanone, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-(4-Hydroxyphenyl)-2-butanone, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
250 g
25 g
100 g
Catalog number A14064.30
also known as A14064-30
Price (USD)/ Each
286.00
-
Add to cart
Quantity:
250 g
Request bulk or custom format
Price (USD)/ Each
286.00
Add to cart
4-(4-Hydroxyphenyl)-2-butanone, 98%, Thermo Scientific Chemicals
Catalog numberA14064.30
Price (USD)/ Each
286.00
-
Add to cart
Chemical Identifiers
CAS5471-51-2
IUPAC Name4-(4-hydroxyphenyl)butan-2-one
Molecular FormulaC10H12O2
InChI KeyNJGBTKGETPDVIK-UHFFFAOYSA-N
SMILESCC(=O)CCC1=CC=C(O)C=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.5%
FormCrystals or powder or crystalline powder or needles
Melting Point (clear melt)80.0-87.0°C
Appearance (Color)White to cream
4-(4-Hydroxyphenyl)-2-butanone is used in perfumery, in cosmetics, and as a food additive to impart a fruity odor.

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
4-(4-Hydroxyphenyl)-2-butanone is used in perfumery, in cosmetics, and as a food additive to impart a fruity odor.

Solubility
Insoluble in water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Giovanni Fronzaa; Claudio Fugantia; Monica Mendozzaa; Roberta S.Rallob; Gianluca Ottolinab; Daniel Joulain. Stereochemistry of the double bond saturation in the formation in baker's yeast of 4-(4-hydroxyphenyl)-2-butanone (raspberry ketone). Tetrahedron. 1996, 52,(11), 4041-4052.
  2. Rolf Andersson; Lennart N.Lundgren. Monoaryl and cyclohexenone glycosides from needles of Pinus sylvestris. Phytochemistry. 1988, 27,(2), 559-562.