W354805
2′-Hydroxyacetophenone
≥98%
Synonym(s):
2-Acetylphenol
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About This Item
Linear Formula:
HOC6H4COCH3
CAS Number:
Molecular Weight:
136.15
FEMA Number:
3548
Beilstein/REAXYS Number:
386123
EC Number:
Council of Europe no.:
4136
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.124
NACRES:
NA.21
organoleptic:
hawthorne; herbaceous; phenolic; sweet
grade:
Fragrance grade
biological source:
synthetic
agency:
follows IFRA guidelines
meets purity specifications of JECFA
meets purity specifications of JECFA
food allergen:
no known allergens
Recommended Products
biological source
synthetic
Quality Level
grade
Fragrance grade
agency
follows IFRA guidelines
meets purity specifications of JECFA
reg. compliance
EU Regulation 1223/2009
vapor density
4.7 (vs air)
vapor pressure
~0.2 mmHg ( 20 °C)
assay
≥98%
refractive index
n20/D 1.558 (lit.)
bp
213 °C/717 mmHg (lit.)
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Related Categories
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
222.8 °F - closed cup
flash_point_c
106 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Shuai Chen et al.
Organic letters, 14(11), 2806-2809 (2012-05-17)
Flavin catalysts perform the first organocatalytic Dakin oxidation of electron-rich arylaldehydes to phenols under mild, basic conditions. Catechols are readily prepared, and the oxidation of 2-hydroxyacetophenone was achieved. Aerobic oxidation is displayed in the presence of Zn(0) as a reducing
José I Borrell et al.
Molecular diversity, 8(2), 147-157 (2004-06-24)
Two new solid-phase syntheses of substituted pyrazoles are described. The first includes supporting an o-hydroxyacetophenone on Merrifield resin, Vilsmeier-Haack formylation on the methyl group and cyclization with a substituted hydrazine to afford a pyrazole ring with two diversity centers. The
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].
R R Zaky et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 683-694 (2012-08-14)
The o-Hydroxy acetophenone [N-(3-hydroxy-2-naphthoyl)] hydrazone (H(2)o-HAHNH) has been prepared and its structure is confirmed by elemental analysis, IR, (1)H NMR and (13)C NMR spectroscopy. It has been used to produce diverse complexes with Co(II), Cd(II), Hg(II) and U(VI)O(2) ions. The
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