159913
Heptanophenone
98%
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About This Item
Fórmula lineal:
C6H5CO(CH2)5CH3
Número de CAS:
Peso molecular:
190.28
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Ensayo
98%
Formulario
liquid
índice de refracción
n20/D 1.5077 (lit.)
bp
155 °C/15 mmHg (lit.)
mp
17 °C (lit.)
densidad
0.946 g/mL at 25 °C (lit.)
cadena SMILES
CCCCCCC(=O)c1ccccc1
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
Clave InChI
UXMQORVHJMUQFD-UHFFFAOYSA-N
Descripción general
Heptanophenone is an alkyl phenyl ketone and its inhibitory effect on carbonyl reductase activity in pig heart has been examined.[1]
Aplicación
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.[2]
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
235.4 °F - closed cup
Punto de inflamabilidad (°C)
113 °C - closed cup
Equipo de protección personal
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
Gert Desmet et al.
Journal of chromatography. A, 1626, 461279-461279 (2020-08-17)
We report on a comparative study of the basic separation kinetics of commercial packed bed columns and a micro-pillar array column (μPAC) working in the 1-10μL/min flow rate range, i.e., operating in the area of capillary flow LC. This is
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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