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Application Note 031003X Analysis of Alkylphenones Using High Pressure Resistance and High Performance Column under High Pressure at 120 MPa Introduction In UHPLC, in order to perform the measurement in short period of time by using a long column offering high resolution and theoretical plates , there needs to apply relatively high flow rate, causing extremely high pressure to be applied to the column. Also, if water/methanol or water/ethanol solvent system is required in gradient elution mode, the extremely high pressure will be caused due to the change of viscosity. For avoiding such potential problems, JASCO now offers the UHPLC system including pump, dynamic mixer and autosampler which can be operated under the extremely high pressure up to 130 MPa (option). In this application note, JASCO X-LC system including such optional UHPLC hardware was applied to the quick analysis of alkylphenones under high pressure (120 MPa pressure) using high pressure resistance and high performance column. Keyword: UHPLC, alkylphenones, 130 MPa, 1.8 m, C18 column, PDA detector Experimental [Equipment] [Conditions] Pump: X-LC 3185PU-130 Column: ZORBAX RRHD SB-C18 (2.1 mmID x 150 mmL, 1.8 m) Degasser: X-LC 3080DG Eluent : Water/Acetonitrile (30/70) Column oven: X-LC 3067CO Flow rate: 1.0 mL/min Autosampler: X-LC 3159AS-130 Column temp.: 40 ºC Detector: X-LC 3110MD Wavelength: 254 nm Injection volume: 1 L Pressure: 120 MPa Standard sample: Acetanilide, Acetophenone, Propiophenone, Butyrophenone Valerophenone, Hexanophenone, Heptanophenone, Octanophenone (2 g/mL each) Results The chromatogram and contour plot of standard mixtures of alkylphenones are shown in Fig. 1. The result was obtained only within two minutes with good separation. 254nm 1: Acetanilide 2: Acetophenone 3: Propiophenone 4: Butyrophenone 5: Valerophenone 6: Hexanophenone 7: Heptanophenone 8: Octanophenone Fig. 1. Chromatogram of Standard Mixtures of Alkylphenones. copyright©JASCO Corporation JASCO INTERNATIONAL CO., LTD 4-21, Sennin-cho 2-chome, Hachioji, Tokyo 193-0835, Japan Tel: +81-42-666-1322, Fax: +81-42-665-6512 1/1 .

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Relative Reactivities of Some Organometallic Compounds Lester D
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1940 Relative reactivities of some organometallic compounds Lester D. Apperson Iowa State College Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Apperson, Lester D., "Relative reactivities of some organometallic compounds " (1940). Retrospective Theses and Dissertations. 13183. https://lib.dr.iastate.edu/rtd/13183 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. NOTE TO USERS This reproduction is the best copy available. UMI BELAflVI REAOflVITIES OP SOME OMANOHSTALlilO COMPOUNDS by Lester D. Apperson A thesis aateltted to the (Graduate Faculty for the Degree of DOCfOR OF PHILOSOPHX Major Subjeot Organic Chemietry Approved! Signature was redacted for privacy. In cha3%e of Major work Signature was redacted for privacy. or Department Signature was redacted for privacy. Dean of Qraduat® College^ Iowa State College 1940 UMI Number: DP12552 INFORMATION TO USERS The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleed-through, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion.
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