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ES5634
ChromegaChiral(TM) Chiral CCS, 10 Micron HPLC Column (C15-1424-582)
Price: $4,170.33List Price: $4,633.70ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5636
ChromegaChiral(TM) Chiral CCS, 10 Micron HPLC Column (C15-1424-583)
Price: $4,170.33List Price: $4,633.70ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5637
ChromegaChiral(TM) Chiral CCS, 10 Micron HPLC Column (C15-1424-584)
Price: $32,571.43List Price: $36,190.48ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5606
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-560)
Price: $4,598.90List Price: $5,109.89ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5607
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-561)
Price: $4,598.90List Price: $5,109.89ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5608
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-562)
Price: $4,598.90List Price: $5,109.89ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5609
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-563)
Price: $4,945.05List Price: $5,494.51ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5610
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-564)
Price: $4,945.05List Price: $5,494.51ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5612
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-565)
Price: $6,214.29List Price: $6,904.76ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5613
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-566)
Price: $6,214.29List Price: $6,904.76ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5614
ChromegaChiral(TM) Chiral CCS, 3 Micron HPLC Column (C15-1424-567)
Price: $6,214.29List Price: $6,904.76ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of -
ES5615
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-568)
Price: $3,593.41List Price: $3,992.67ChromegaChiral CCS (amylose tris [(S)-a-methylbenzylcarbamate]) permits the enantiomeric separation of 1-Indanol without the addition of DEA (Diethyl amine). Historically DEA has been commonly used to improve peak shape for chiral separations of