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48292

Supelco

Acetophenone solution

certified reference material, 2000 μg/mL in methylene chloride

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Empirical Formula (Hill Notation):
C8H8O
CAS Number:
Molecular Weight:
120.15
EC Number:

grade

certified reference material

Quality Level

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

2000 μg/mL in methylene chloride

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-30°C

InChI

1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3

InChI key

KWOLFJPFCHCOCG-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation markHealth hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 2

Regulatory Information

危险化学品

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V Selvarani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 91, 329-337 (2012-03-14)
Four tetradentate (N(2)O(2)) and tridentate (NO(2)) Schiff base compounds (L1-L4) with propargyl moiety were prepared by the condensation of 1-[2-hydroxy-4-(prop-2-yn-1-yloxy)phenyl]ethanone with various aliphatic amines. The newly synthesized compounds (L1-L4) were characterized on the basis of the results of elemental analysis
Xinzheng Yang
Inorganic chemistry, 50(24), 12836-12843 (2011-11-23)
The hydrogenation of ketones catalyzed by 2,6-bis(diisopropylphosphinomethyl)pyridine (PNP)-ligated iron pincer complexes was studied using the range-separated and dispersion-corrected ωB97X-D functional in conjunction with the all-electron 6-31++G(d,p) basis set. A validated structural model in which the experimental isopropyl groups were replaced
Manickam Sugumaran et al.
Insect biochemistry and molecular biology, 43(2), 209-218 (2013-01-01)
Arterenone (2-amino-3',4'-dihydroxy acetophenone) is an important hydrolytic product generated from lightly colored sclerotized cuticle that use N-acyldopamine derivatives for crosslinking reactions. It seems to arise from 1,2-dehydro-N-acetyldopamine (dehydro NADA) that has been crosslinked to the cuticular components. However, the mechanism
Eric R Bittner et al.
The Journal of chemical physics, 137(22), 22A551-22A551 (2012-12-20)
The standard model for molecular recognition of an odorant is that receptor sites discriminate by molecular geometry as evidenced that two chiral molecules may smell very differently. However, recent studies of isotopically labeled olfactants indicate that there may be a
Simon Gane et al.
PloS one, 8(1), e55780-e55780 (2013-02-02)
Whether olfaction recognizes odorants by their shape, their molecular vibrations, or both remains an open and controversial question. A convenient way to address it is to test for odor character differences between deuterated and undeuterated odorant isotopomers, since these have

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