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Acetophenone solution

certified reference material, 2000 μg/mL in methylene chloride

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

Quality Level


certified reference material


current certificate can be downloaded


ampule of 1 mL


2000 μg/mL in methylene chloride


HPLC: suitable
gas chromatography (GC): suitable

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single component solution

storage temp.

room temp



InChI key


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


Exclamation markHealth hazard

Signal Word


Hazard Statements

Hazard Classifications

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

Target Organs

Central nervous system

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK Germany


Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

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...
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...
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...
Yuka Inatomi et al.
Journal of natural medicines, 67(2), 359-368 (2012-08-01)
New glycosides of seven acetophenone derivatives (1-7) and two phenylpropanoids (8, 9), named juniperosides III-XI, have been isolated from the MeOH extract of the leaves and stems of Juniperus occidentalis Hook. (Cupressaceae), together with eleven other known compounds. The structures...
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...


HPLC Analysis of Benzene and Deuterated Benzene on Ascentis® Express C18

HPLC Analysis of Benzene and Deuterated Benzene on Ascentis® Express C18

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

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