Chiral Columns for enantiomer separation by HPLC

Similar documents
Handling Products. Sumitomo Chemical Co., Ltd. SUMICHIRAL ~192

TCI Chiral HPLC Column

CHIRAL STATIONARY PHASES

LIQUID CHROMATOGRAPHY

Analysis - HPLC A.136. Primesep 5 µm columns B.136

Optical Isomer Separation Columns and Packing Materials

6 Optical Isomer Separation Columns

COPYRIGHTED MATERIAL INTRODUCTION

8. Methods in Developing Mobile Phase Condition for C18 Column

ChromegaChiral TM CSP Media and Columns

CHIRAL SEPARATION USING THIN LAYER CHROMATOGRAPHY

CHROMTECH - CHIRAL HPLC COLUMNS

Journal of Chromatography A

Ch.28 HPLC. Basic types of Liquid Chromatography Partition (LLC) Adsorption (LSC) Ion Exchange (IC) Size Exclusion (SEC or Gel Chromatography)

ChromegaChiral TM CSP Media and Columns

Packings for HPLC. Packings for HPLC

Chiral Flash Columns

The Theory of HPLC. Normal Phase (Absorption) Chromatography

penta-hilic UHPLC COLUMNS

Enantiomer Separation of Chiral Acids on CHIRALPAK AX-QN and CHIRALPAK AX QD

Aromatic Hydrocarbons

An HPLC column offering moderate retentivity with superb peak shape Inertsil ODS Sprint

guanidine bisurea bifunctional organocatalyst

Chromatography 1 of 26 Boardworks Ltd 2016

HICHROM. Chromatography Columns and Supplies. LC COLUMNS SIELC Primesep. Catalogue 9. Hichrom Limited

columns Acclaim Mixed-Mode WCX-1 for Separating Basic Molecules

High Performance Liquid Chromatography

High Performance Liquid Chromatography

Epic Aromatic Selectivity

Fast Separation of Vastly Different Compounds by Isocratic HPLC

Comparison of different aqueous mobile phase HPLC techniques

Measuring enzyme (enantio)selectivity

Asymmetric Transfer Hydrogenation: A Suitable Tool for the Synthesis of the Precursors of Pharmaceutical Substances

INTRODUCTION. Amino acids occurring in nature have the general structure shown below:

penta-hilic UHPLC COLUMNS

Colin F. Poole Department of Chemistry Wayne State University USA

High Performance Liquid Chromatography

Advantages of polymerbased. an alternative for ODS

High Pressure/Performance Liquid Chromatography (HPLC)

Shodex TM ODP2 HP series columns

QUALITY HPLC COLUMNS PARTICLE PORE PAGE SIZE SIZE. C18 Bidentate C18 Extremely long column life and rugged 4um 100Å 3

A New Model for Asymmetric Amplification in Amino Acid Catalysis - Supporting information

Open Column Chromatography, GC, TLC, and HPLC

Thermo Scientific Syncronis HPLC Columns. Remarkable separations guaranteed time after time

HICHROM. Chromatography Columns and Supplies. LC COLUMNS SeQuant ZIC-HILIC. Catalogue 9. Hichrom Limited

Application Note. Authors. Abstract. Pharmaceuticals

SEPARATION OF FLURBIPROFEN AND IBUPROFEN ENANTIOMERS ON A CHIRAL STATIONARY PHASE USING SUPERCRITICAL FLUIDS

Acclaim Mixed-Mode WCX-1

Cation Exchange HPLC Columns

FAQ's. 1 - Which column would be the most appropriate for my application?

CHAPTER 1 Role of Bioanalytical Methods in Drug Discovery and Development

Acclaim Mixed-Mode WAX-1 Columns

Supporting Information

LUMEFANTRINUM LUMEFANTRINE

UNIT 4 REVISION CHECKLIST CHEM 4 AS Chemistry

Liquid Chromatographic Resolution of Fendiline and Its Analogues on a Chiral Stationary Phase Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid

Downstream Processing Prof. Mukesh Doble Department Of Biotechnology Indian Institute of Technology, Madras. Lecture - 33 HPLC

for Acclaim Mixed-Mode WCX-1

Inertsil ODS-EP Technical Information

Agilent s New Weak Anion Exchange (WAX) Solid Phase Extraction Cartridges: SampliQ WAX

MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

10/4/2010. Sequence Rules for Specifying Configuration. Sequence Rules for Specifying Configuration. 5.5 Sequence Rules for Specifying.

Astec CHIROBIOTIC. Macrocyclic Glycopeptide-Based Chiral HPLC Phases

Gas Chromatography. Vaporization of sample Gas-solid Physical absorption Gas-liquid Liquid immobilized on inert solid

TLC Introduction. tlc Choose Stationary Phase. Select Visualization Technique. Choose a Mobile Phase

Sample Preparation TLC Plates

Capacity vs Throughput on Modified Macrocylics in Reversed Phase, Polar Ionic Mode and Normal Phase

Chiral Method Development in LC/MS Using Macrocyclic Glycopeptide CSPs

Chapter content. Reference

How proteins separate on reverse-phase HPLC

Fall Organic Chemistry Experiment #6 Fractional Crystallization (Resolution of Enantiomers)

LC and LC/MS Column Selection Flow Chart

Amino Acids, Polypeptides and Proteins. An -amino acid is a carboxylic acid which has an amino group attached to the carbon to the COOH.

Chemistry Instrumental Analysis Lecture 28. Chem 4631

Experiment : Reduction of Ethyl Acetoacetate

Lab.2. Thin layer chromatography

EVALUATION OF EXPERIMENTAL PARAMETER INFLUENCE ON HPLC SEPARATION OF SOME AMINES AND

Chromatography. Gas Chromatography

Zirconia-Based Phases as a Powerful Complement to Silica-Based Phases for LC and LC-MS under Non-extreme Mobile Phase Conditions

zorbax Packed by Phenomenex Material Characteristics High efficiency Guaranteed quality Phenomenex columns packed with Zorbax

Supporting Information

An alcohol is a compound obtained by substituting a hydoxyl group ( OH) for an H atom on a carbon atom of a hydrocarbon group.

Multi-Prep and Detectabuse Columns and 96 Well Deep-Well Plates for Sample Preparation

William E. Barber, Ph.D. Applications Chemist October

SPE Introduction. general chromatography. solid phase extraction. How to Choose an SPE Product. Solid-Phase Processing Methods

ADVANTAME. Not less than 97.0% and not more than 102.0% on the anhydrous basis. Sweetener, flavour enhancer

Chapter 4. Carbon and the Molecular Diversity of Life. AP Biology Parkway Central H.S. A. Bergeron

INSTRUCTION MANUAL FOR CHIRALPAK ZWIX(+) and CHIRALPAK ZWIX(-)

Small Molecule Selectivity Sampler

Suggested solutions for Chapter 41

CHROMATOGRAPHY: LIQUID

HICHROM. Chromatography Columns and Supplies. LC COLUMNS Thermo Scientific Acclaim. Catalogue 9. Hichrom Limited

for Acclaim Mixed-Mode HILIC-1 Column

Page 2. The tripeptide shown is formed from the amino acids alanine, threonine and lysine.

Lecture 2. The framework to build materials and understand properties

HPLC Background Chem 250 F 2008 Page 1 of 24

Chapter 25 Organic and Biological Chemistry

GL Chromatodisc. Usage Type Description. GL Chromatodisc Type A GL Chromatodisc Type P GL Chromatodisc Type N 13AI

ChromegaChiral TM Columns. The right choice for chiral purification

Naming Organic Halides. Properties of Organic Halides

Transcription:

Chiral Columns for enantiomer separation by HPLC SUMICHIRAL OA columns are high-performance chiral columns for enantiomer separation by HPLC. On SUMICHIRAL OA columns direct separation of various enantiomers can be realized effectively. Enantiomeric separation is achieved from the various diastereomeric interactions such as hydrogen bonding, charge transfer and host-guest interactions, etc. SUMICHIRAL OA columns are very useful for the accurate determination of the optical purity and for the preparation of pure enantiomers of biologically active compounds such as pharmaceuticals, pesticides, and perfumes.

Improved Pirkle Type 1 Amide Type : Asymmetric carbon atoms are bonded directly with CONH group OA-2000 series have a 3,5-dinitrobenzoyl group as the-acid and may interact with the solute molecule by charge transfer, hydrogen bonding, etc. The enantiomers of aromatic compounds, esters, carboxylic acids and alcohols may be directly separated on OA-2000 series. OA-2000 is especially effective for pyrethroidal esters, OA-2500 for carboxylic acids such as profen-drugs. Urea Type : Asymmetric carbon atoms are bonded directly with NHCONH group OA-3000 series have 3,5-dinitrophenylurea group as the-acid and, in the reverse phase mode, promote chiral discrimination by charge transfer, hydrogen bonding, etc. In general OA-3000 series are effective for carboxylic acids, and especially for acetyl- and urethane-amino acids, dansylamino acids. OA-3300 offers good direct separation for profen-drugs, acetyl-amino acids, BOC-amino acids and benzyl-amino acids. Main columns : SUMICHIRAL OA-2500, SUMICHIRAL OA-3300 < Pesticide > < Profen-drugs > Fenvalerate Ketoprofen Naproxen SUMICHIRAL OA-2000 (2504.6mm) Mobile Phase : hexane / 1,2-dichloroethane / ethanol (500 / 30 / 0.15) Detector : UV230nm SUMICHIRAL OA-2500 (2504.6mm) Mobile Phase : 0.03mol/L ammonium SUMICHIRAL OA-2500 (2504.6mm) Mobile Phase : 0.05mol/L ammonium < Amino acid N-derivatives > < Atropisomer > BOC-Phenylalanine Dansyl-Valine 1,1 -Binaphthol SUMICHIRAL OA-3300 (2504.6mm) Mobile Phase : 0.01mol/L ammonium Flow Rate : 0.6mL/min SUMICHIRAL OA-3200 (2504.6mm) Mobile Phase : 0.01mol/L ammonium SUMICHIRAL OA-3300 (2504.6mm) Mobile Phase : hexane / 2-propanol / methanol (70 / 20 / 10)

SUMICHIRAL OA The large number of theoretical plates of the columns offer high resolution. The packing materials have chemical stability and the columns have long life. The enantiomeric stationary phases give the inverse elution orders and so accurate determination of the optical purity and efficient preparation of the enantiomer are attained. Improved Pirkle Type 2 Two chiral centers at amine and amino acid are bonded with NHCONH group OA-4000 series have a naphthyl group as the-base, and two chiral centers at amine and amino acid group. By charge transfer, hydrogen bonding, etc., chiral discrimination is acheived, and a wide variety of compounds such as pharmaceuticals of amine and amino alcohols, alcohols, esters and amides can be directly resolved in the normal phase mode. Amide and urethane derivatives of amines, alcohols, etc. can be resolved effectively. Main columns : SUMICHIRAL OA- 4700, SUMICHIRAL OA- 4900 < Amine-type drugs > Tolperizone Isoproterenol Chlormezanone SUMICHIRAL OA-4500 (2504.6mm) Mobile Phase : hexane / tetrahydrofuran / methanol / trifluoroacetic acid ( 60 / 35 / 5 / 0.2 ) SUMICHIRAL OA-4900 (2504.6mm) Mobile Phase : hexane /1,2-dichloroethane / methanol / trifluoroacetic acid ( 240 / 140 / 20 / 1 ) Flow Rate : 1.0mL/min Detector : UV280nm SUMICHIRAL OA-4700 (2504.6mm) Mobile Phase : hexane / 2-propanol / methanol / trifluoroacetic acid ( 80 / 15 / 5 / 0.2 ) Detector :UV254nm

Ligand exchange Type The chiral components are coated hydrophobically on ODS OA-5000 and 6000 series offer chiral discrimination by ligand exchange interaction in the reversed phase mode. The chiral ligands such as penicillamine (OA-5000) or tartaric acid derivatives (OA-6000 series) are coated on ODS silica, though the volume of organic solvents added to the mobile phase is limited. Mobile phases including Cu ++ ions are used in these columns. They are effective for direct enantiomer separation of not only amino acids, hydroxy acids but also copper-chelate forming compounds such as amino alcohols, diamines, dicarboxylic acids, aminolactames and dipeptides. Especially OA-5000 can be applied for extremely wide range, while OA-6100 is effective for -amino acids,-hydroxy acids and hydrophilic amino acids. Main columns : SUMICHIRAL OA-5000, SUMICHIRAL OA-6100 < Amino acids > Tryptophan Valine Baclofen SUMICHIRAL OA-6100 (1504.6mm) in water / acetonitrile (90/10) Flow Rate : 1.0mL/min SUMICHIRAL OA-5000 (1504.6mm) in water / 2-propanol (95/5) SUMICHIRAL OA-5000 (1504.6mm) in water / 2-propanol (85/15) Detector : UV280nm < Hydroxy acids > ( Inversion of elution order ) Mandelic acid Lactic acid Lactic acid SUMICHIRAL OA-6100 (1504.6mm) in water / acetonitrile (90/10) SUMICHIRAL OA-5000 (1504.6mm) Mobile Phase : 2mmol/L copper (II) sulfate in water / acetonitrile (95/5) SUMICHIRAL OA-5000L (1504.6mm) Mobile Phase : 2mmol/L copper () sulfate in water / acetonitrile (95/5) Flow Rate : 1.0mL/min

Host-Guest Type Cyclodextrin bonded chiral stationary phase with novel spacer OA-7000 is a novel chiral stationary phase with -cyclodextrin bonded to the silica gel via new type of spacer. A large number of racemates, including ketones, amines, and amino acid derivatives can be separated under reversed phase conditions. (1) Sharp peaks and high theoretical plate numbers are obtained. Improved peak shape is due to the effect of hydrophilic spacer moiety which prevents secondary interactions between the silica gel and the sample molecules. (2) Popular reversed phase conditions can be used. Novel Chiral Stationary phase bonded with crown ether OA-8000 is a novel chiral stationary phase bonded with chiral crown ether to aminopropyl silica gel. This is very effective for enantiomer separations of amines, aminoalcohols and amino acids, especially for hydrophobic amines. (1) Stationary phase is covalent bond type and very stable. (2) Both reversed and normal phases can be used. (3) Sharp peaks and high theoretical plate numbers are obtained < Aromatic compounds > Flavanone Cyclopentrate Chlorthalidone SUMICHIRAL OA-7000 (2504.6mm) Mobile Phase : 20mmol/L phosphate buffer (ph2.0) / acetonitrile (60:40) Flow Rate : 0.85mL/min, SUMICHIRAL OA-7000 (2504.6mm) Mobile Phase : 20mmol/L phosphate buffer (ph3.0) / acetonitrile (60:40) Flow Rate : 0.2mL/min SUMICHIRAL OA-7000 (2504.6mm) Mobile Phase : 20mmol/L phosphate buffer (ph3.0) / acetonitrile (80:20) Flow Rate : 0.7mL/min < Primary amine and aminoalcohol > < Amino acid > 1-(1-Naphthyl)-ethylamine Phenylpropanolamine Cysteine SUMICHIRAL OA-8000 (2504.6mm) Mobile Phase : perchloric acid in water (ph2.0) / acetonitrile (70 / 30) Flow Rate : 0.7mL/min, SUMICHIRAL OA-8000 (2504.6mm) Mobile Phase : hexane / ethanol / trifluoroacetic acid (70 /30 /0.5) Flow Rate : 0.7mL/min SUMICHIRAL OA-8000 (2504.6mm) Mobile Phase : hexane / ethanol / trifluoro-acetic acid (70 /30 /0.5) Flow Rate : 0.7mL/min

SUMICHIRAL OA Standard type Inverted type Mode** SUMICHIRAL Chiral component SUMICHIRAL OA-2000 (R)-phenylglycine OA-2000S NP OA-2500 (R)-1-naphthylglycine OA-2500S RP OA-3100 (S)-valine OA-3100R NP,RP OA-3200 (S)-tert-leucine OA-3200R NP,RP OA-3300 (R)-phenylglycine OA-3300S NP,RP OA-4000 (S)-valine (S)-1-(-naphthyl)ethylamine OA-4000R NP OA-4100 (S)-valine (R)-1-(-naphthyl)ethylamine OA-4100R NP OA-4400 (S)-proline (S)-1-(-naphthyl)ethylamine OA-4400R NP OA-4500 (S)-proline (R)-1-(-naphthyl)ethylamine OA-4500R NP OA-4600 (S)-tert-leucine (S)-1-(-naphthyl)ethylamine OA-4600R NP OA-4700 (S)-tert-leucine (R)-1-(-naphthyl)ethylamine OA-4700R NP OA-4800 OA-4900 (S)-indoline-2-carboxylic acid (S)-1-(-naphthyl)ethylamine (S)-indoline-2-carboxylic acid (R)-1-(-naphthyl)ethylamine OA-5000 (D)-penicillamine OA-5000L RP OA-6000 (L)-tartaric acid (S)-1-(-naphthyl)ethylamine OA-6000R RP OA-6100 (L)-tartaric acid, (S)-valine (R)-1-(-naphthyl)ethylamine OA-6100R OA-7000 -cyclodextrin with novel spacer RP OA-8000 chiral pseudo 18-crown-6 ether NP,RP Most popular phases * Enantiomeric stationary phases (inversed types) are available except for OA-4800, 4900, 7000 and 8000, and on these phases the elution order of enantiomer are inversed. ** NP : normal phase mode, RP : reversed phased mode Standard column dimensions NP NP RP Guard column Analitical column Preparative column 4.0mm10mm, 8mm50mm 4.6mm250mm 4.6mm150mm is also available for OA-8000. 4.6mm150mm ( for OA-5000,6000,6100 ) 4.6mm50mm is also available for OA-5000. 8mm250mm, 10mm250mm, 20mm250mm Distributor SUMIKA CHEMICAL ANALYSIS SERVICE, Ltd. Chromatography Column Section 3-1-135, Kasugade-naka, Konohanaku, Osaka, 554-0022, Japan, URL http://www.scas.co.jp Fax + 81-6-6466-5255 TEL +81-6-6466-5243 E-Mail column@scas.co.jp