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Safety Information

48292

Supelco

Acetophenone solution

certified reference material, 2000 μg/mL in methylene chloride

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About This Item

Empirical Formula (Hill Notation):
C8H8O
CAS Number:
98-86-2
Molecular Weight:
120.15
EC Number:
200-838-9
UNSPSC Code:
12000000

grade

certified reference material

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

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H336,H351

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

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

危险化学品

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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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
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
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
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