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H18607

Sigma-Aldrich

2′-Hydroxyacetophenone

ReagentPlus®, 99%

Synonym(s):

2-Acetylphenol

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About This Item

Linear Formula:
HOC6H4COCH3
CAS Number:
118-93-4
Molecular Weight:
136.15
Beilstein:
386123
EC Number:
204-288-0
MDL number:
MFCD00002219
UNSPSC Code:
12352100
PubChem Substance ID:
24895486
NACRES:
NA.22

vapor density

4.7 (vs air)

vapor pressure

~0.2 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99%

form

liquid

refractive index

n20/D 1.558 (lit.)

bp

213 °C/717 mmHg (lit.)

mp

3-6 °C (lit.)

density

1.133 g/mL at 20 °C
1.131 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1ccccc1O

InChI

1S/C8H8O2/c1-6(9)7-4-2-3-5-8(7)10/h2-5,10H,1H3

InChI key

JECYUBVRTQDVAT-UHFFFAOYSA-N

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

222.8 °F - closed cup

Flash Point(C)

106 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mohammed Y Merza et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(7), 1677-1683 (2004-05-19)
Ultra violet absorption spectra of o-methylacetophenone, o-fluoroacetophenone and o-hydroxyacetophenone solutions in different solvents are recorded in the region 200-350 nm at room temperature. Excited state dipole moments for three (pi* <-- pi) transitions of the benzene ring for solutions in
Daniele Gabriel et al.
Journal of cardiovascular pharmacology, 57(1), 20-27 (2011-01-15)
Isatin (1H-indole-2,3 dione) is an endogenous compound with biological activities. Many of its derivatives have pharmacological effects, including inhibition of cyclic guanosine monophosphate levels in cardiac tissue; sedative-hypnotic profiles; anticonvulsant, analgesic, antithermic, and anti-inflammatory activities; and anxiolytic, antimicrobial, and proapoptotic
Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12595-12598 (2012-08-29)
Flavone of the month: a general and efficient method for the palladium-catalyzed carbonylative synthesis of flavones has been developed. Starting from aryl bromides and 2-hydroxyacetophenones, the corresponding flavones have been isolated in good yields.
Synthesis and pharmacological evaluation of some potential beta-adrenolytics derivated from o-hydroxyacetophenone.
R Cizmáriková et al.
Die Pharmazie, 49(5), 366-367 (1994-05-01)
Rohith P John et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(6), 1349-1358 (2003-03-28)
The spectral studies and structure of a ternary complex of copper(II) with 2-hydroxyacetophenone 3-hexamethyliminylthiosemicarbazonate (L(2-)) and 1,10-phenanthroline (phen) are reported. The thiosemicarbazone binds to the metal as a dianionic ONS-donor (L(2-)) ligand, and forms a complex of the stoichiometry [CuLphen].
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