159913
Heptanophenone
98%
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About This Item
Linear Formula:
C6H5CO(CH2)5CH3
CAS Number:
Molecular Weight:
190.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-802-0
MDL number:
Assay:
98%
Form:
liquid
InChI key
UXMQORVHJMUQFD-UHFFFAOYSA-N
InChI
1S/C13H18O/c1-2-3-4-8-11-13(14)12-9-6-5-7-10-12/h5-7,9-10H,2-4,8,11H2,1H3
SMILES string
CCCCCCC(=O)c1ccccc1
assay
98%
form
liquid
refractive index
n20/D 1.5077 (lit.)
bp
155 °C/15 mmHg (lit.)
mp
17 °C (lit.)
density
0.946 g/mL at 25 °C (lit.)
General description
Heptanophenone is an alkyl phenyl ketone and its inhibitory effect on carbonyl reductase activity in pig heart has been examined.
Application
Heptanophenone was employed as test compound to compare the kinetic performance of monolithic and fused-core capillary C(18) columns in isocratic-elution liquid chromatography.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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.)
Tünde A Diószegi et al.
Journal of chromatography. A, 1261, 107-112 (2012-09-12)
The kinetic performance of monolithic and fused-core capillary C(18) columns was compared in isocratic-elution liquid chromatography. Heptanophenone was chosen as a test compound. The (u(0), H) couple obtained in a column with permeability K(v0) was transferred into a plate number
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
Erin P Shields et al.
Journal of chromatography. A, 1618, 460851-460851 (2020-02-06)
Mixed-mode cation-exchange stationary phases are useful for the separation of mixtures containing hydrophobic, acidic, and basic molecules. To ensure that weak organic bases are protonated and carboxylic acids are neutral low pH mobile phases are required. Mixed-mode stationary phases that
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