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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 -
ES5617
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-569)
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 -
ES5620
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-570)
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 -
ES5622
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-571)
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 -
ES5623
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-572)
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 -
ES5624
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-573)
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 -
ES5625
ChromegaChiral(TM) Chiral CCS, 5 Micron HPLC Column (C15-1424-574)
Price: $13,071.43List Price: $14,523.81ChromegaChiral 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