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48292

Supelco

Acetophenone solution

certified reference material, 2000 μg/mL in methylene chloride

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About This Item

Fórmula empírica (Notação de Hill):
C8H8O
Número CAS:
98-86-2
Peso molecular:
120.15
Número CE:
200-838-9
Código UNSPSC:
12000000

grau

certified reference material

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 1 mL

concentração

2000 μg/mL in methylene chloride

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

environmental

formato

single component solution

temperatura de armazenamento

2-30°C

InChI

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

chave InChI

KWOLFJPFCHCOCG-UHFFFAOYSA-N

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Aplicação

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

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H336,H351

Classificações de perigo

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

Órgãos-alvo

Central nervous system

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
LRAD2491
LRAC1113
XA16659V
XA16633V
LC08087

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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
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
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
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