APPLICATIONS TN HPLC Conditions. Lux Cellulose-1 Cellulose tris(3,5-dimethylphenylcarbamate)

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T-147 APPLICATIS Alternative Selectivity of Chiral Stationary Phases Based on Cellulose tris(3-chloro-4-methylphenylcarbamate) and Cellulose tris(3,5-dimethylphenylcarbamate) Liming Peng, Tivadar Farkas and Swapna Jayapalan Phenomenex, Inc., 411 Madrid Ave., Torrance, CA 951 USA Introduction Polysaccharide-based chiral stationary phases (CSP) are widely used due to their wide chiral recognition ability. Several cellulose and amylose derivatives are extremely effective in the separation of a wide range of compounds of interest in the pharmaceutical industry 1. This work demonstrates the different chiral recognition capabilities of CSPs based on cellulose tris(3-chloro-4- methylphenylcarbamate) and cellulose tris(3,5-dimethylphenylcarbamate). ver 18 racemates of pharmaceutical interest were analyzed on these two phases in normal (P), polar-organic (P) and reversed phase (RP) separation modes. umerous examples including important classes of drug compounds as well as statistical data prove that cellulose tris(3-chloro-4 methylphenylcarbamate) offers a good alternative to the commonly used cellulose tris(3,5- dimethylphenylcarbamate) in the separation of difficult racemic mixtures. Figure 1. Structures of Chiral Selective Phases Cellulose-1 Cellulose tris(3,5-dimethylphenylcarbamate) HPLC Conditions Instrumentation HPLC System: Agilent 11 series (www.agilent.com) Pump: G1311A Quaternary Pump Autosampler: G1313A ALS HPLC Conditions Detector: G1315A Diode Array Detector Flow Rate: 1. ml/min Injection Volume: 5-2 μl (depending on analyte response) Sample 5 μg/ml racemate dissolved in mobile phase Concentration: Columns: 5 μm Cellulose-1; 25 x 4.6 mm 5 μm Cellulose-2; 25 x 4.6 mm CHIRALCEL 5 μm D-H ; 25 x 4.6 mm Detector: UV @ 22 nm Table 1. Mobile Phase Compositions Mobile Phase P P Basic and eutral Compounds Acidic and eutral Compounds.1 % DEA in Hexane:IPA.1 % HAC (or FA) in Hexane:IPA.1 % DEA in MeH:IPA.1 % HAC (or FA) in MeH:IPA.1 % DEA in CH 3 C:IPA.1 % HAC (or FA) in CH 3 C:IPA IPA: Iso-propanol; DEA: Diethylamine; HAC: Acetic Acid; FA: Formic acid; MeH: Methanol; CH 3 C: Acetonitrile Cellulose-2 Cellulose tris(3-chlorlo-4-methyl-dimethylphenylcarbamate) Page 1 of 8

T-147 APPLICATIS Figure 2. Enantioseparations of ß-Blockers in ormal Phase Toliprolol on Cellulose-1.1 % DEA in Hexane /.1 % DEA in IPA (8:2) 4 2 4 2 Toliprolol on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (8:2) Toliprolol on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (9:1) App ID 17478 1 2 min App ID 17479 1 2 min xprenolol on Cellulose-1.1 % DEA in Hexane /.1 % DEA in IPA (9:1) 4 2 4 2 4 8 min xprenolol on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (9:1) 4 8 min Column: 5 µm Cellulose-1 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E G-4457-E Detection: UV @ 22 nm H H xprenolol App ID 17481 App ID 17482 H 4 2 Column: 5 µm Cellulose-1 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E G-4457-E Detection: UV @ 22 nm App ID 1748 1 2 min H Bopindolol on Cellulose-1.1 % DEA in Hexane /.1 % DEA in IPA (9:1) 8 4 Bopindolol on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (9:1) 4 8 min App ID 17483 H 8 Toliprolol 4 4 8 min App ID 17484 Column: 5 µm Cellulose-1 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E G-4457-E Detection: UV @ 22 nm H H Bopindolol Page 2 of 8

T-147 APPLICATIS Figure 3. Enantioseparations in ormal Phase Warfarin on Cellulose-1.1 % Formic Acid in Hexane /.1 % Formic Acid in IPA (6:4) 4 Rs: 7.41 Sulcanozole on Cellulose-1.1 % DEA in Hexane /.1 % DEA in IPA (6:4) 4 Rs: 2.37 2 App ID 17311 2 App ID 17324 4 8 min 1 2 min Warfarin on Cellulose-2.1 % Formic Acid in Hexane /.1 % Formic Acid in IPA (6:4) 4 2 Column: 5 µm Cellulose-1 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E G-4457-E Detection: UV @ 22 nm Rs: 3.12 4 8 min App ID 17312 Sulcanozole on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (6:4) 4 2 1 2 min Column: 5 µm Cellulose-1 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E G-4457-E Detection: UV @ 22 nm Rs: 5.9 App ID 17325 Warfarin on CHIRALCEL D-H.1 % Formic Acid in Hexane /.1 % Formic Acid in IPA (6:4) Sulcanozole on CHIRALCEL D-H.1 % DEA in Hexane /.1 % DEA in IPA (6:4) 4 Rs: 4.4 4 Rs: 2.19 2 App ID 17313 2 App ID 17326 4 8 min 1 2 min Column: CHIRALCEL 5 µm D-H Dimensions: 25 x 4.6 mm ID Detection: UV @ 22 nm Column: CHIRALCEL 5 µm D-H Dimensions: 25 x 4.6 mm ID Detection: UV @ 22 nm S H Warfarin Sulconazole *with.1 % Formic Acid CHIRALCEL and D-H are registered trademarks of DAICEL Chemical Industries, Ltd. Comparative separations may not be representative of all applications. Page 3 of 8

T-147 APPLICATIS Figure 4. Complementary Enantioselectivity in ormal Phase and Polar-rganic Sulcanozole on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (6:4) 4 2 Sulcanozole on Cellulose-2.1 % DEA in MeH /.1 % DEA in IPA (95:5) 6 4 2 Sulcanozole on Cellulose-2.1 % DEA in CH 3 C /.1 % DEA in IPA (95:5) 2 Rs: 5.8 1 2 min Rs:. 4 8 min Rs: 2.54 4 8 12 min App ID 17485 App ID 17325 App ID 17513 Milnacipran on Cellulose-2.1 % DEA in Hexane /.1 % DEA in IPA (8:2 ) 12 1 8 6 4 2 Milnacipran on Cellulose-2.1 % DEA in MeH /.1 % DEA in IPA (9:1) 1 8 6 4 2 Milnacipran on Cellulose-2.1 % DEA in CH 3 C /.1 % DEA in IPA (95:5) 4 2 Rs: 1.12 4 8 12 min Rs: 4.28 4 8 12 min o Elution 4 8 12 min App ID 17492 App ID 17488 App ID 17489 Column: 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4457-E Detection: UV @ 22 nm S Column: 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4457-E Detection: UV @ 22 nm H H Sulconazole Milnacipran Page 4 of 8

T-147 APPLICATIS Figure 4. (cont d) Complementary Enantioselectivity in ormal Phase and Polar-rganic Figure 5. Enantioseparations in Reversed Phase Chlormezanone on Cellulose-1.1 % DEA in CH3C /.1 % DEA in IPA (6:4) 1 enbuterol on Cellulose-2.1 % DEA in MeH /.1 % DEA in Water (8:2) Rs:. 12 Rs:.51 App ID 17728 8 4 App ID 1754 4 8 12 min 1 2 min Chlormezanone on Cellulose-1.1 % DEA in CH3C /.1 % DEA in IPA (95:5) 1 Rs:. App ID 17729 enbuterol on Cellulose-2.1 % DEA in CH 3 C /.1 % DEA in Water (6:4) 12 8 4 Rs:.97 4 8 12 min App ID 1755 Chlormezanone on Cellulose-1.1 % DEA in MeH /.1 % DEA in IPA (9:1) 4 Column: 5 µm Cellulose-1 Dimensions: 25 x 4.6 mm ID Part o.: G-4459-E Detection: UV @ 22 nm 4 8 min 1 S 2 Chlormezanone App ID 1773 8 min CH 3 Rs: 3.21 CI enbuterol on Cellulose-2.1 % DEA in CH 3 C /.1 % DEA in Water (4:6) 8 6 4 2 4 8 12 min Column: 5 µm Cellulose-2 Dimensions: 25 x 4.6 mm ID Part o.: G-4457-E Detection: UV @ 22 nm Mobile Phase Rs Hexane:IPA. MeH:IPA. CH 3 C. H 2 Rs: 1.46 enbuterol H H App ID 1756 Page 5 of 8

T-147 APPLICATIS Figure 6. Success Rates for over 18 Racemates on Cellulose-1 and -2 8 75 71 67 73 68 2 6 55 26 31 26 11 31 2 4 25 26 11 18 18 25 2 18 18 13 9 11 12 6 9 9 11 5 Cellulose-1 (MeH) Cellulose-2 (MeH) Cellulose-1 (CH 3 C) Cellulose-2 (CH 3 C) Cellulose-1 (P) Cellulose-2 (P) umero totale di separazioni Separazione parziale sia su Cellulose-1 che su Cellulose-2 Separazione alla linea di base sia su Cellulose-1 che su Cellulose-2 Separazione parziale Separazione alla linea di base Page 6 of 8

T-147 APPLICATIS Results and Discussion, a new line of polysaccharide-based chiral selective phases, has recently been introduced into the market. ne phase, Cellulose-1 is based on cellulose tris (3,5- dimethylphenyl carbamate) similar to other chiral phases on the market (e.g. CHIRACEL D-H ). The other phase, Cellulose-2, is a new member to the family of polysaccharide based chiral selective phases and uses cellulose tris (3-chloro-4-methylphenyl carbamate) (Figure 1) as a chiral selector; this new chemistry delivers a unique selectivity versus other phases 2,3. In this study over 18 diverse compounds of pharmaceutical interest were screened on the line of chiral selective phases as well as other comparative medias to better characterize the selectivity delivered by each phase. Table 1 summarizes the screening conditions used for each column; different types of mobile phases (P, P, and RP) as well as additives used (.1 formic acid or acetic acid for acidic analytes or.1% diethylamine for basic analytes). Figures 2-5 show several representative examples of the different selectivities provided by Cellulose-1 and Cellulose-2 in chiral separations across normal phase, polar-organic and reversed phase separation modes. Representative compounds such as various ß-blockers, warfarin, sulconazole, milnacipran, and clenbuterol demonstrate the complementary behavior of Cellulose-2 to the commonly used cellulose tris (3.5-dimethylphenylcarbamate) based CSPs (CHIRACEL D-H and Cellulose-1) in the separation of difficult racemates. Figure 2 demonstrates the behavior of the two phases in normal phase separations. While Cellulose-1 generally demonstrates slightly better resolution and increased retention versus CHIRACEL D-H, there are several cases where Cellulose-2 is a better separation choice when using normal phase. While Bopindolol is equally well separated on the two phases, xprenolol enantiomers are better resolved on Cellulose-2. Toliprolol enantomers are separated on Celluose-1 with spectacular resolution but at the expense of extensive retention for one of the enantomers. Cellulose-2 barely separates racemic xprenolol under similar mobile phase conditions, but with minimal optimization (i.e. a reduction of IPA in the mobile phase) a better separation is achieved with Cellulose-2 with significantly shorter analysis time. Figure 3 shows additional normal phase enantomeric separations using Cellulose-1, Cellulose-2 and CHIRACEL D-H. Such separations further demonstrate the complementary selectivity offered by Cellulose-2 versus the cellulose tris (3,5-dimethylphenyl carbamate) phases Cellulose-1 and CHI- RACEL D-H. EW Figure 6 compares the success rates of Cellulose-1 and Cellulose-2 in the analysis of over 18 racemates in normal phase or polar organic separation modes. The number of uniquely baseline resolved racemates are given at the bottom of the bar graph. The same selection criteria was applied to partially separated racemates. For example, Cellulose-2 shows good chiral recognition in acetonitrile mobile phase with 9 baseline separations of racemates that could not be separated on Cellulose-1. This complementary enantioselectivity of Cellulose-2 over Cellulose-1 is most evident in acetonitrile: IPA mobile phase mixtures, and is less pronounced in standard normal phase mixtures (hexane / IPA) and methanol mixtures. References 1. Y. kamoto, Y. Kaida J. Chromatography A 666 (1994), 43-419 2.. Matthijs, M. Maftouh, Y. Vander Heyden J. Chromatography A 1111 (26), 48-61 3. T. Huybrechts, G. Torrok, T. Vennekens, R. Sneyers, S. Vrielynck, I. Somers LCGC Europe June 1, 27 4.. Maier, P. Franco, W. Lindner J. Chromatography A 96 (21), 3-33 rdering Information 5 µm Analytical Columns (mm) Phase 1 x 4.6 15 x 4.6 25 x 4.6 Cellulose-1 D-4459-E F-4459-E G-4459-E Cellulose-2 D-4457-E F-4457-E G-4457-E Amylose-2 D-4472-E F-4472-E G-4472-E phases are available in 3 µm, 5 µm and 2 µm and many other dimensions. Figures 4 and 5 demonstrate the effect of mobile phase composition on chiral resolution. Figure 4 demonstrates the dramatic changes in selectivity for each phase when traditional normal phase separation is substituted with polar organic separation mode using either acetonitrile or methanol as mobile phase. Figure 5 shows changes in selectivity are observed in reversed phase mode. Different solvents can alter the steric structure of the polysaccharide backbone and the arrangement of binding sites 4, providing alternative selectivity for separating difficult chiral compounds. Such mobile phase alteration offers a powerful tool in developing and optimizing chiral separations. CHIRALCEL and D-H are registered trademarks of DAICEL Chemical Industries, Ltd. Comparative separations may not be representative of all applications. Page 7 of 8

T-147 APPLICATIS Australia t: 2-9428-6444 f: 2-9428-6445 auinfo@phenomenex.com Austria t: 1-319-131 f: 1-319-13 anfrage@phenomenex.com Belgium t: +31 ()3-24187 f: +31 ()3-2383749 beinfo@phenomenex.com Canada t: (8) 543-3681 f: (31) 328-7768 info@phenomenex.com Denmark t: 4824 848 f: 481 6265 dkinfo@phenomenex.com France t: 1 3 9 21 1 f: 1 3 9 21 11 franceinfo@phenomenex.com Germany t: 621-5883- f: 621-5883-11 anfrage@phenomenex.com Ireland t: 1 247 545 f: +44 1625-51796 eireinfo@phenomenex.com Italy t: 51 6327511 f: 51 6327555 italiainfo@phenomenex.com embourg t: +31 ()3-24187 f: +31 ()3-2383749 nlinfo@phenomenex.com etherlands t: 3-24187 f: 3-2383749 nlinfo@phenomenex.com ew Zealand t: 9-478951 f: 9-478952 nzinfo@phenomenex.com Puerto Rico t: (8) 541-HPLC f: (31) 328-7768 info@phenomenex.com United Kingdom t: 1625-51367 f: 1625-51796 ukinfo@phenomenex.com All other countries: Corporate ffice USA t: (31) 212-555 f: (31) 328-7768 info@phenomenex.com www.phenomenex.com Phenomenex products are available worldwide. For the distributor in your country, contact Phenomenex USA, International Department at international@phenomenex.com. Trademarks is a trademark of Phenomenex, Inc. CHIRALCEL and D-H are registered trademarks of DAICEL Chemical Industries, Ltd. of Japan. Disclaimer Comparative separations may not be representative of all applications. Subject to Phenomenex Standard Terms & Conditions, which may be viewed at www.phenomenex.com/termsandconditions. 28 Phenomenex, Inc. All rights reserved. T63878_L Page 8 of 8