159913
Heptanophenone
98%
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About This Item
Formule linéaire :
C6H5CO(CH2)5CH3
Numéro CAS:
Poids moléculaire :
190.28
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Pureté
98%
Forme
liquid
Indice de réfraction
n20/D 1.5077 (lit.)
Point d'ébullition
155 °C/15 mmHg (lit.)
Pf
17 °C (lit.)
Densité
0.946 g/mL at 25 °C (lit.)
Chaîne 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
Clé InChI
UXMQORVHJMUQFD-UHFFFAOYSA-N
Description générale
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.
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
235.4 °F - closed cup
Point d'éclair (°C)
113 °C - closed cup
Équipement de protection individuelle
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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