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48292

Supelco

Acetophenone solution

certified reference material, 2000 μg/mL in methylene chloride

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About This Item

Formula empirica (notazione di Hill):
C8H8O
Numero CAS:
98-86-2
Peso molecolare:
120.15
Numero CE:
200-838-9
Codice UNSPSC:
12000000

Grado

certified reference material

CdA

current certificate can be downloaded

Confezionamento

ampule of 1 mL

Concentrazione

2000 μg/mL in methylene chloride

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

environmental

Formato

single component solution

Temperatura di conservazione

2-30°C

InChI

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

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Applicazioni

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

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H336,H351

Classi di pericolo

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

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
LRAD2491
LRAC1113
XA16659V
XA16633V
LC08087

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Slide 1 of 4

1 of 4

Acetophenone for synthesis

Sigma-Aldrich

8.00028

Acetophenone

Acetophenone ≥98%, FG

Sigma-Aldrich

W200905

Acetophenone

C8-C40 Alkanes Calibration Standard in dichloromethane (varied)

Supelco

40147-U

C8-C40 Alkanes Calibration Standard

C4 - C24 Even Carbon Saturated FAMEs 1000 μg/mL each component in hexane, analytical standard

Supelco

49453-U

C4 - C24 Even Carbon Saturated FAMEs

Dejan Vražič et al.
Molecules (Basel, Switzerland), 18(1), 74-96 (2013-01-25)
The Brønsted-acidic ionic liquid 1-methyl-3-(4-sulfobutyl)imidazolium triflate [BMIM(SO(3)H)][OTf] was demonstrated to act efficiently as solvent and catalyst for the halogenation of activated organic compounds with N-halosuccinimides (NXS) under mild conditions with short reaction times. Methyl aryl ketones were converted into α-halo
Raphaël F Guignard et al.
Chemical communications (Cambridge, England), 47(44), 12185-12187 (2011-10-15)
A new concise route to Polycyclic Aromatic Hydrocarbons (PAHs) through radical addition and cyclisation of xanthates is described.
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
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