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319775

Sigma-Aldrich

Octanophenone

≥99%

Synonym(s):

Caprylophenone

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About This Item

Linear Formula:
CH3(CH2)4COC6H5
CAS Number:
1674-37-9
Molecular Weight:
204.31
Beilstein:
1868534
EC Number:
216-817-2
MDL number:
MFCD00003554
UNSPSC Code:
12352100
PubChem Substance ID:
24859188
NACRES:
NA.22

Assay

≥99%

form

liquid

refractive index

n20/D 1.5044 (lit.)

bp

285-290 °C (lit.)

mp

21.5-23.5 °C (lit.)

density

0.936 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCC(=O)c1ccccc1

InChI

1S/C14H20O/c1-2-3-4-5-9-12-14(15)13-10-7-6-8-11-13/h6-8,10-11H,2-5,9,12H2,1H3

InChI key

UDEVCZRUNOLVLU-UHFFFAOYSA-N

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Shunta Futagami et al.
Journal of chromatography. A, 1595, 58-65 (2019-02-26)
We report on the ability to change the layer properties of porous layered radially elongated pillar (PLREP) array columns and its relevance to the separation efficiency. The adjustment of the preparation condition resulted in the formation of a 1.2-fold thicker
Gert Desmet et al.
Journal of chromatography. A, 1626, 461339-461339 (2020-08-17)
We report on a systematic and comprehensive (0.7 ≤ k'' ≤ 122) experimental study of the effect of the zone retention factor k'' on eddy dispersion (heddy) in packed bed columns for liquid chromatography. The values for heddy are obtained by subtracting
Sam Wouters et al.
Journal of chromatography. A, 1523, 224-233 (2017-06-18)
The present paper discusses practical aspects of prototyping of microfluidic chips using cyclic olefin copolymer as substrate and the application in high-performance liquid chromatography. The developed chips feature a 60mm long straight separation channel with circular cross section (500μm i.d.)
Shunta Futagami et al.
The Analyst, 144(5), 1809-1817 (2019-01-24)
The performance of a porous-layered radially elongated pillar (PLREP) array column in a commercial nano-LC system was examined by performing separation of alkylphenones and peptides. The mesoporous silica layer was prepared by sol-gel processing of a mixture of tetramethoxysilane and
Erin P Shields et al.
Journal of chromatography. A, 1598, 132-140 (2019-04-15)
Stationary phases that can withstand extremes of pH and temperature are needed to allow a single column to accommodate a wider set of solutes and separation criteria. We used a simple multi-step process using the thiol-yne reaction following the modification
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