Skip to Content
Merck
All Photos(2)

Key Documents

137227

Sigma-Aldrich

1-Phenyl-2-butanone

98%

Synonym(s):

Benzyl ethyl ketone

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5CH2COC2H5
CAS Number:
Molecular Weight:
148.20
Beilstein:
1100022
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.512 (lit.)

bp

109-112 °C/15 mmHg (lit.)

density

0.998 g/mL at 25 °C (lit.)

functional group

ketone
phenyl

SMILES string

CCC(=O)Cc1ccccc1

InChI

1S/C10H12O/c1-2-10(11)8-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

InChI key

GKDLTXYXODKDEA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1-Phenyl-2-butanone was used in the preparation of 1-bromo-1-phenyl-2-butanone. It was used as solute to evaluate the hydroxyl group-solvent and carbonyl group-solvent specific interactions in acetonitrile/water mixtures using the alltima C18 stationary phase by HPLC.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

The hydroxyl group-solvent and carbonyl group-solvent specific interactions for some selected solutes including positional isomers in acetonitrile/water mixed solvents monitored by HPLC.
Cheong WJ, et al.
Bull. Korean Chem. Soc., 23(1), 65-70 (2002)
Charles W Schindler et al.
The Journal of pharmacology and experimental therapeutics, 376(1), 118-126 (2020-10-22)
Dietary supplements often contain additives not listed on the label, including α-ethyl homologs of amphetamine such as N,α-diethylphenethylamine (DEPEA). Here, we examined the neurochemical and cardiovascular effects of α-ethylphenethylamine (AEPEA), N-methyl-α-ethylphenethylamine (MEPEA), and DEPEA as compared with the effects of
A rapid radiometric assay for mammalian cytosolic epoxide hydrolase.
C A Mullin et al.
Analytical biochemistry, 106(2), 476-485 (1980-08-01)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service