Chemical Analysis

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Title
Description
Article Nr.
Chromatogram VCR0037J Chiral separation of 1-(Naphthalene-6-yl)Ethane-1,2-diol

k´1 = 7.98; k´2 = 6.63; α = 1.20;

VCR0037J

Chromatogram VCR0010J Chiral separation of 1-Aza[6]Helicene

k´1 = 1.28; k´2 = 1.59; α = 1.24;

VCR0010J

Chromatogram VCR0011J Chiral separation of 1-Benzene-2-Naphthene-3-Amino Propan(1)ol

k´1 = 2.46; k´2 = 3.13; α = 1.27;

VCR0011J

Chromatogram VCR0039J Chiral separation of 1-Phenylethylenglycol (1-Phenylethane1,2-diol)

k´1 = 3.65; k´2 = 3.98; α = 1.09;

VCR0039J

Chromatogram VCR0040J Chiral separation of 1-Phenylpropane-1,2-diol

k´1 = 2.76; k´2 = 2.93; α = 1.06;

VCR0040J

Chromatogram VCR0050J Chiral separation of 1,1´-Bi-2-Naphthol (BINOL)

tR1 = 5.19 min; tR2 = 5.71 min;

VCR0050J

Chromatogram VCR0026J Chiral separation of 1,2-Diphenyl-2-(Tosylamino)Ethanone

k´1 = 7.66; k´2 = 8.66; α = 1.13;

VCR0026J

Chromatogram VCR0016J Chiral separation of 2,2´Bis(Diphenylphosphinoxid)3,3´Bibenzo[b]Thiophene

k´1 = 2.45; k´2 = 2.99; α = 1.22;

VCR0016J

Chromatogram VCR0007J Chiral separation of 3-Amino-2(2-Naphtyl)-1-Phenyl-Propanol

k´1 = 2.46; k´2 = 3.13; α = 1.27;

VCR0007J

Chromatogram VCR0018J Chiral separation of 4-Bromphenyl-Glycinamid (2-(4-Bromphenyl)-2-Amino Acetamid)

k´1 = 3.09; k´2 = 4.54; α = 1.47;

VCR0018J

Chromatogram VCR0013J Chiral separation of a - Benzoylbenzylbutyrate

k´1 = 1.63; k´2 = 2.37; α = 1.45;

VCR0013J

Chromatogram VCR0047J Chiral separation of a - Tocopherole

k´1 = 2.40; k´2 = 2.93; α = 1.22;

VCR0047J

Chromatogram VCR0005J Chiral separation of Abscisic Acid (4-Oxo-2-Cyclohexen-1-yl)-3-Methyl-2,4-Pentanedienoic Acid)

k´1 = 2.67; k´2 = 3.19; α = 1.19;

VCR0005J

Chromatogram VCR0008J Chiral separation of Atenolol (2-[4-[2-Hydroxy-3-(1-Methylethylamino)Propoxy]Phenyl]Ethanamid)

k´1 = 6.53; k´2 = 8.17; α = 1.25;

VCR0008J

Chromatogram VCR0009J Chiral separation of Atropine (rac-Hyoscyamin)

k´1 = 0.54; k´2 = 0.89; α = 1.65;

VCR0009J

Chromatogram VCR0012J Chiral separation of Benzoin (a-Hydroxy-a-Phenylacetophenon)

k´1 = 7.18; k´2 = 11.33; α = 1.58;

VCR0012J

Chromatogram VCR0014J Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3-Phenylpropionate)

k´1 = 0.31; k´2 = 0.40; α = 1.29;

VCR0014J

Chromatogram VCR0015J Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3Phenylpropionate)

k´1 = 0.75; k´2 = 1.62; α = 2.16;

VCR0015J

Chromatogram VCR0049J Chiral separation of Benzyl-Mandelate (Benzyl-2-Hydroxy-3Phenylpropionate)

tR1 = 2.23 min; tR2 = 2.96 min;

VCR0049J

Chromatogram VCR0055J Chiral separation of Carazolol I

k´1 = 0.20; k´2 = 0.38; α = 1.9;

VCR0055J

Chromatogram VCR0056J Chiral separation of Carazolol II

k´1 = 0.97; k´2 = 1.56; α = 1.6;

VCR0056J

Chromatogram VCR0019J Chiral separation of Carbinoxamine (2-[(4-Chlorophenyl)Pyridin-2-yl-Methoxy]-N,N-Dimethyl-Ethanamine)

k´1 = 1.69; k´2 = 1.94; α = 1.14;

VCR0019J

Chromatogram VCR0021J Chiral separation of Clenbuterol

k´1 = 4,95; k´2 = 5,64; α = 1,14;

VCR0021J

Chromatogram VCR0022J Chiral separation of Cyanofenphos

k´1 = 5.50; k´2 = 8.55; α = 1.56;

VCR0022J

Chromatogram VCR0023J Chiral separation of Diclofop – methyl

k´1 = 1.21; k´2 = 3.23; α = 2.67;

VCR0023J

Chromatogram VCR0024J Chiral separation of Dihydrofuranone

k´1 = 23.7; k´2 = 26.3; α = 1.1;

VCR0024J

Chromatogram VCR0027J Chiral separation of Ethyl-Mandelate

k´1 = 1.10; k´2 = 2.32; α = 2.11;

VCR0027J

Chromatogram VCR0051J Chiral separation of Ethyl-Mandelate

tR1 = 1.71 min; tR2 = 2.04 min;

VCR0051J

Chromatogram VCR0028J Chiral separation of Etozolin (Ethyl(3-Methyl-4-Oxo-5Piperidinothiazolidin-2-ylidene)Acetate)

k´1 = 0.68; k´2 = 1.05; α = 1.54;

VCR0028J

Chromatogram VCR0029J Chiral separation of Flavanone (2-Phenyl-1,4-Benzopyrone)

k´1 = 1.41; k´2 = 1.83; α = 1.30;

VCR0029J

Chromatogram VCR0030J Chiral separation of Hexahydro-6,6-Dimethyl-2-Tosylpyrrolo [1,2-e]Imidazol-3-one

k´1 = 3.92; k´2 = 4.92; α = 1.25;

VCR0030J

Chromatogram VCR0052J Chiral separation of Hydrobenzoin (1,2-Diphenylethane-1,2diol)

tR1 = 2.95 min; tR2 = 3.24 min;

VCR0052J

Chromatogram VCR0031J Chiral separation of Hydroxyzine

k´1 = 1.88; k´2 = 2.15; α = 1.14;

VCR0031J

Chromatogram VCR0032J Chiral separation of Lactic Acid

k´1 = 2.99; k´2 = 3.47; α = 1.16;

VCR0032J

Chromatogram VCR0033J Chiral separation of Mandelic acid

k´1 = 0.49 ; k´2 = 0.70 ; α = 1.43 ;

VCR0033J

Chromatogram VCR0035J Chiral separation of Methyl phenyl sulfoxide

k´1 = 4.65; k´2 = 5.52; α = 1.18;

VCR0035J

Chromatogram VCR0001J Chiral separation of Methyl phenyl sulfoxide II

k´1 = 3.77; k´2 = 5.35; α = 1.42;

VCR0001J

Chromatogram VCR0036J Chiral separation of Metoprolol (1-(Isoppropylamino)-3-[4-(2Methoxyethyl)Phenoxy]Propan-2-ol)

k´1 = 1.34; k´2 = 1.96; α = 1.46;

VCR0036J

Chromatogram VCR0034J Chiral separation of n-Methylephedrin (2-Dimethylamino-1Phenyl-Propanol)

k´1 = 0.88; k´2 = 1.25; α = 1.42;

VCR0034J

Chromatogram VCR0038J Chiral separation of Naproxen (6-Methoxy-a-Methyl-2Naphthylessigsäure)

k´1 = 0.97; k´2 = 1.17; α = 1.21;

VCR0038J

Chromatogram VCR0042J Chiral separation of Pindolol (1-(1H-Indol-4-yloxy)3-(1-Methylethylamino)Propan-2-ol)

k´1 = 0.6; k´2 = 1.37; α = 2.28;

VCR0042J

Chromatogram VCR0041J Chiral separation of Pindolol (1-(1H-Indol-4-yloxy)3-(1-Methylethylamino)Propan-2-ol)

k´1 = 1.43; k´2 = 3.68; α = 2.57;

VCR0041J

Chromatogram VCR0043J Chiral separation of Praziquantel

k´1 = 0.44; k´2 = 0.54; α = 1.23;

VCR0043J

Chromatogram VCR0045J Chiral separation of Propranolol (1-Isopropylamino3-(1-Naphthyloxy)-2-Propanol)

k´1 = 1.75; k´2 = 2.49; α = 1.42;

VCR0045J

Chromatogram VCR0044J Chiral separation of Propranolol (1-Isopropylamino3-(1-Naphthyloxy)-2-Propanol)

k´1 = 12.8; k´2 = 14.32; α = 1.12;

VCR0044J

Chromatogram VCR0053J Chiral separation of trans Stilbene Oxide

tR1 = 2.12 min; tR2 = 2.52 min;

VCR0053J

Chromatogram VCR0046J Chiral separation of trans-Stilbene oxide

k´1 = 0.74; k´2 = 1.01; α = 1.37;

VCR0046J

Chromatogram VCR0048J Chiral separation of Warfarin (4-Hydroxy-3-(3-Oxo-1-PhenylButyl)-Cumarin)

k´1 = 2.88; k´2 = 4.39; α = 1.53;

VCR0048J

Chromatogram VCR0054J Chiral separation of Warfarin (4-Hydroxy-3-(3-Oxo-1-PhenylButyl)-Cumarin)

tR1 = 3.26 min; tR2 = 4.98 min;

VCR0054J

Chromatogram VCH0002J Determination of aromatic Hydrocarbon types in middle distillates acc. to prEN 12916:2006

Retention time standard; 1. Cyclohexane; 2. Phenyldodecane; 3. 1,2 Dimethylbenzene; 4. Hexamethylbenzene; 5. Naphthalene; 6. Dibenzothiophene; 7. 9-Methylanthracene; Calibration standard; 8. 1,2 Dimethylbenzene; 9. Fluorene; 10. Phenanthrene; Sample; 11. MAH 20.14% [m/m]; 12. DAH 2.33% [m/m]; 13. T+AH 0.11% [m/m]; Total aromatic hydrocarbens:; 22.59 % [m/m];

VCH0002J