ChromegaChiral CC3 Prep

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ChromegaChiral CC3 (amylose tris(5-chloro-2-methyl- phenylcarbamate) is a new product for high resolution chiral separations based on a new halogenated carbohy- drate based chiral stationary phase. Similar in selectivity to ChiralPak® AY-H.

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    ChromegaChiral CC3

    ChromegaChiral CC3 (amylose tris(5-chloro-2-methyl- phenylcarbamate) is a new product for high resolution chiral separations based on a new halogenated carbohy- drate based chiral stationary phase. Similar in selectivity to ChiralPak® AY-H.

    ChromegaChiral CCO F2

    ChromegaChiral CCO F2 – The addition of a fluorine atom into a phenyl carbamate cellulose structure can be useful in promoting fluorophilic retention mechanism which can provide improved retention for fluorinated compounds (1). A fluorophilic retention mechanism can be particularly useful in medicinal chemistry and drug discovery, where more than a third of newly approved small molecule drugs contain fluorine (2). ChromegaChiral CCO F2 is a 2-Fluoro 5-methylphenyl cellulose phase which can be used in SFC or HPLC.

    ChromegaChiral CCO F4 T3 Prep

    ChromegaChiral CCO F4 T3 (4-Fluoro-3-(trifluoromethyl) phenyl cellulose) incorporates fluoro groups into its structure. The addition of a fluorine atom into a phenyl cellulose structure can be useful in promoting fluorophilic retention mechanism which can provide improved retention for fluorinated compounds (1). A fluorophilic retention mechanism can be particular useful in medicinal chemistry and drug discovery, where more than a third of newly approved small molecule drugs contain fluorine (2). ChromegaChiral CCO-F4T3 is 4-Fluoro-3-(trifluoromethyl) phenyl cellulose phase can be used in SFC or HPLC.

    ChromegaChiral CCJ Prep

    ChromegaChiral CCJ (cellulose 4-methylbenzoate) is a new product for high resolution chiral separations based on a new halogenated carbohydrate based chiral stationary phase. Similar in selectivity to ChiralPak® OJ-H.

    ChromegaChiral CCC Prep

    ChromegaChiral CCC is a modified cellulose including the combination of 3-chloro-4 methylphenylcarbamate and 3,5-dichloro- phenylcarbamate bonding groups coated on high purity, high performance spherical silica particles. This combination of bonded groups stabilizes the solubility of coated phase making for a durable phase similar to other widely used coated phases. The use of cellulose modified with chlorinated phenyl groups provides for the separation for many previously unresolved/poorly resolved chiral mixtures by providing unique separation characteristics.

    ChromegaChiral CCC

    ChromegaChiral CCC is a modified cellulose including the combination of 3-chloro-4 methylphenylcarbamate and 3,5-dichloro- phenylcarbamate bonding groups coated on high purity, high performance spherical silica particles. This combination of bonded groups stabilizes the solubility of coated phase making for a durable phase similar to other widely used coated phases. The use of cellulose modified with chlorinated phenyl groups provides for the separation for many previously unresolved/poorly resolved chiral mixtures by providing unique separation characteristics.

    ChromegaChiral CCO F2 Prep

    ChromegaChiral CCO F2 – The addition of a fluorine atom into a phenyl carbamate cellulose structure can be useful in promoting fluorophilic retention mechanism which can provide improved retention for fluorinated compounds (1). A fluorophilic retention mechanism can be particularly useful in medicinal chemistry and drug discovery, where more than a third of newly approved small molecule drugs contain fluorine (2). ChromegaChiral CCO F2 is a 2-Fluoro 5-methylphenyl cellulose phase which can be used in SFC or HPLC.

    ChromegaChiral CCX

    ChromegaChiral CCX is a modified amylose coated on the high purity, high performance spherical silica particles. The chemical modification includes the combination of chemical bonding groups of methylbenzylcarbamate and 3,5-dimetheylphenylcarbamate attached to amylose. This combination of bonded groups stabilizes the solubility of coated phase making for a durable phase similar to other widely used coated phases. The use of amylose modified with phenyl groups provides for the separation for many previously unresolved/poorly resolved chiral mixtures.