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Titel
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Artikelnummer
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Beschreibung
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Chiral separation of 1-(Naphthalene-6-yl)Ethane-1,2-diol
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VCR0037J
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k´1 = 7.98; k´2 = 6.63; α = 1.20;
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Chiral separation of 1-Aza[6]Helicene
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VCR0010J
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k´1 = 1.28; k´2 = 1.59; α = 1.24;
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Chiral separation of 1-Benzene-2-Naphthene-3-Amino Propan(1)ol
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VCR0011J
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k´1 = 2.46; k´2 = 3.13; α = 1.27;
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Chiral separation of 1-Phenylethylenglycol (1-Phenylethane1,2-diol)
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VCR0039J
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k´1 = 3.65; k´2 = 3.98; α = 1.09;
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Chiral separation of 1-Phenylpropane-1,2-diol
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VCR0040J
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k´1 = 2.76; k´2 = 2.93; α = 1.06;
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Chiral separation of 1,1´-Bi-2-Naphthol (BINOL)
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VCR0050J
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tR1 = 5.19 min; tR2 = 5.71 min;
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Chiral separation of 1,2-Diphenyl-2-(Tosylamino)Ethanone
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VCR0026J
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k´1 = 7.66; k´2 = 8.66; α = 1.13;
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Chiral separation of 2,2´Bis(Diphenylphosphinoxid)3,3´Bibenzo[b]Thiophene
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VCR0016J
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k´1 = 2.45; k´2 = 2.99; α = 1.22;
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Chiral separation of 3-Amino-2(2-Naphtyl)-1-Phenyl-Propanol
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VCR0007J
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k´1 = 2.46; k´2 = 3.13; α = 1.27;
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Chiral separation of 4-Bromphenyl-Glycinamid (2-(4-Bromphenyl)-2-Amino Acetamid)
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VCR0018J
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k´1 = 3.09; k´2 = 4.54; α = 1.47;
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Chiral separation of a - Benzoylbenzylbutyrate
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VCR0013J
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k´1 = 1.63; k´2 = 2.37; α = 1.45;
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Chiral separation of a - Tocopherole
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VCR0047J
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k´1 = 2.40; k´2 = 2.93; α = 1.22;
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Chiral separation of Abscisic Acid (4-Oxo-2-Cyclohexen-1-yl)-3-Methyl-2,4-Pentanedienoic Acid)
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VCR0005J
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k´1 = 2.67; k´2 = 3.19; α = 1.19;
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Chiral separation of Alprenolol
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VCR0006J
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k´1 = 0.46; k´2 = 1.38; α = 2.99;
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Chiral separation of Atenolol (2-[4-[2-Hydroxy-3-(1-Methylethylamino)Propoxy]Phenyl]Ethanamid)
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VCR0008J
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k´1 = 6.53; k´2 = 8.17; α = 1.25;
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Chiral separation of Atropine (rac-Hyoscyamin)
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VCR0009J
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k´1 = 0.54; k´2 = 0.89; α = 1.65;
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Chiral separation of Benzoin (a-Hydroxy-a-Phenylacetophenon)
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VCR0012J
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k´1 = 7.18; k´2 = 11.33; α = 1.58;
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Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3-Phenylpropionate)
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VCR0014J
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k´1 = 0.31; k´2 = 0.40; α = 1.29;
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Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3Phenylpropionate)
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VCR0015J
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k´1 = 0.75; k´2 = 1.62; α = 2.16;
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Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3Phenylpropionate)
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VCR0049J
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tR1 = 2.23 min; tR2 = 2.96 min;
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Chiral separation of BITIANP 2,2´Bis(Diphenylphosphino)3,3´Bibenzo[b]Thiophene
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VCR0017J
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k´1 = 1.47; k´2 = 1.71; α = 1.16;
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Chiral separation of Carazolol I
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VCR0055J
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k´1 = 0.20; k´2 = 0.38; α = 1.9;
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Chiral separation of Carazolol II
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VCR0056J
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k´1 = 0.97; k´2 = 1.56; α = 1.6;
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Chiral separation of Carbinoxamine (2-[(4-Chlorophenyl)Pyridin-2-yl-Methoxy]-N,N-Dimethyl-Ethanamine)
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VCR0019J
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k´1 = 1.69; k´2 = 1.94; α = 1.14;
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Chiral separation of Citalopram (1-(3-Dimethylaminopropyl)-1(4-Fluorphenyl)-3H-2-Benzofuran-5-Carbonitrile)
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VCR0020J
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k´1 = 2.67; k´2 = 3.27; α = 1.23;
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Chiral separation of Clenbuterol
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VCR0021J
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k´1 = 4,95; k´2 = 5,64; α = 1,14;
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Chiral separation of Cyanofenphos
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VCR0022J
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k´1 = 5.50; k´2 = 8.55; α = 1.56;
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Chiral separation of Diclofop – methyl
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VCR0023J
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k´1 = 1.21; k´2 = 3.23; α = 2.67;
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Chiral separation of Dihydrofuranone
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VCR0024J
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k´1 = 23.7; k´2 = 26.3; α = 1.1;
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Chiral separation of Dilactid
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VCR0025J
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k´1 = 2.01; k´2 = 2.22; α = 1.10;
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Chiral separation of Ethyl-Mandelate
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VCR0027J
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k´1 = 1.10; k´2 = 2.32; α = 2.11;
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Chiral separation of Ethyl-Mandelate
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VCR0051J
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tR1 = 1.71 min; tR2 = 2.04 min;
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Chiral separation of Etozolin (Ethyl(3-Methyl-4-Oxo-5Piperidinothiazolidin-2-ylidene)Acetate)
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VCR0028J
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k´1 = 0.68; k´2 = 1.05; α = 1.54;
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Chiral separation of Flavanone (2-Phenyl-1,4-Benzopyrone)
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VCR0029J
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k´1 = 1.41; k´2 = 1.83; α = 1.30;
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Chiral separation of Hexahydro-6,6-Dimethyl-2-Tosylpyrrolo [1,2-e]Imidazol-3-one
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VCR0030J
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k´1 = 3.92; k´2 = 4.92; α = 1.25;
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Chiral separation of Hydrobenzoin (1,2-Diphenylethane-1,2diol)
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VCR0052J
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tR1 = 2.95 min; tR2 = 3.24 min;
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Chiral separation of Hydroxyzine
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VCR0031J
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k´1 = 1.88; k´2 = 2.15; α = 1.14;
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Chiral separation of Lactic Acid
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VCR0032J
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k´1 = 2.99; k´2 = 3.47; α = 1.16;
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Chiral separation of Mandelic acid
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VCR0033J
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k´1 = 0.49 ; k´2 = 0.70 ; α = 1.43 ;
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Chiral separation of Methyl phenyl sulfoxide
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VCR0035J
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k´1 = 4.65; k´2 = 5.52; α = 1.18;
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Chiral separation of Methyl phenyl sulfoxide II
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VCR0001J
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k´1 = 3.77; k´2 = 5.35; α = 1.42;
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Chiral separation of Metoprolol (1-(Isoppropylamino)-3-[4-(2Methoxyethyl)Phenoxy]Propan-2-ol)
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VCR0036J
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k´1 = 1.34; k´2 = 1.96; α = 1.46;
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Chiral separation of n-Methylephedrin (2-Dimethylamino-1Phenyl-Propanol)
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VCR0034J
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k´1 = 0.88; k´2 = 1.25; α = 1.42;
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Chiral separation of Naproxen (6-Methoxy-a-Methyl-2Naphthylessigsäure)
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VCR0038J
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k´1 = 0.97; k´2 = 1.17; α = 1.21;
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Chiral separation of Pindolol (1-(1H-Indol-4-yloxy)3-(1-Methylethylamino)Propan-2-ol)
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VCR0042J
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k´1 = 0.6; k´2 = 1.37; α = 2.28;
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Chiral separation of Pindolol (1-(1H-Indol-4-yloxy)3-(1-Methylethylamino)Propan-2-ol)
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VCR0041J
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k´1 = 1.43; k´2 = 3.68; α = 2.57;
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Chiral separation of Praziquantel
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VCR0043J
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k´1 = 0.44; k´2 = 0.54; α = 1.23;
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Chiral separation of Propranolol (1-Isopropylamino3-(1-Naphthyloxy)-2-Propanol)
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VCR0045J
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k´1 = 1.75; k´2 = 2.49; α = 1.42;
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Chiral separation of Propranolol (1-Isopropylamino3-(1-Naphthyloxy)-2-Propanol)
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VCR0044J
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k´1 = 12.8; k´2 = 14.32; α = 1.12;
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Chiral separation of trans Stilbene Oxide
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VCR0053J
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tR1 = 2.12 min; tR2 = 2.52 min;
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