last updated Friday, August 14, 2009 Introduction Thin-layer chromatography (TLC) is a very commonly used technique in synthetic chemistry for identifying compounds, determining their purity and following the progress of a reaction. It also permits the optimization of the solvent system for a given separation problem. In comparison with column chromatography, it only requires small quantities of the compound (~ng) and is much faster as well. Stationary Phase As stationary phase, a special finely ground matrix (silica gel, alumina, or similar material) is coated on a glass plate, a metal or a plastic film as a thin layer (~0.25 mm). In addition a binder like gypsum is mixed into the stationary phase to make it stick better to the slide. In many cases, a fluorescent powder is mixed into the stationary phase to simplify the visualization later on (e.g. bright green when you expose it to 254 nm UV light). Preparing the Plate Do not touch the TLC plate on the side with the white surface. In order to obtain an imaginary start line, make two notches on each side of the TLC plate. You can also draw a thin line with pencil. Do not use pen. Why? The start line should be 0.5-1 cm from the bottom of the plate. Capillary spotters Place a melting point capillary and in the dark blue part of the Bunsen burner flame. Hold it there until it softens and starts to sag. Quickly remove the capillary from the flame and pull on both ends to about 2-3 times its original length. If you pull the capillary inside the flame, you will have a \"piece of art\", but not a good spotter. Allow the capillary to cool down, and then break it in the middle. Make sure that you break off the closed end on one of them. Do not use gloves when you pull capillaries. You will have much better control without them! Watch movie how to pull capillaries here here Spotting the plate The thin end of the spotter is placed in the dilute solution; the solution will rise up in the capillary (capillary forces). Touch the plate briefly at the start line. Allow the solvent to evaporate and spot at the same place again. This way you will get a concentrated and small spot. Try to avoid spotting too much material, because this will deteriorate the quality of the separation considerably (‘tailing’). The spots should be far enough away from the edges and from each other as well. If possible, you should spot the compound or mixture together with the starting materials and possible intermediates on the plate. They will serve as internal reference since every TLC plate is slightly different. Developing a Plate A TLC plate can be developed in a beaker or closed jar (see picture below). Place a small amount of solvent (= mobile phase) in the container. The solvent level has to be below the starting line of the TLC, otherwise the spots will dissolve away. The lower edge of the plate is then dipped in a solvent. The solvent (eluent) travels up the matrix by capillarity, moving the components of the samples at v.

1. last updated Friday, August 14, 2009 Introduction Thin-layer chromatography
(TLC) is a very commonly used technique in synthetic chemistry for identifying compounds,
determining their purity and following the progress of a reaction. It also permits the optimization
of the solvent system for a given separation problem. In comparison with column
chromatography, it only requires small quantities of the compound (~ng) and is much faster as
well. Stationary Phase As stationary phase, a special finely ground matrix (silica gel, alumina,
or similar material) is coated on a glass plate, a metal or a plastic film as a thin layer (~0.25 mm).
In addition a binder like gypsum is mixed into the stationary phase to make it stick better to the
slide. In many cases, a fluorescent powder is mixed into the stationary phase to simplify the
visualization later on (e.g. bright green when you expose it to 254 nm UV light). Preparing the
Plate Do not touch the TLC plate on the side with the white surface. In order to obtain an
imaginary start line, make two notches on each side of the TLC plate. You can also draw a thin
line with pencil. Do not use pen. Why? The start line should be 0.5-1 cm from the bottom of the
plate. Capillary spotters Place a melting point capillary and in the dark blue part of the
Bunsen burner flame. Hold it there until it softens and starts to sag. Quickly remove the capillary
from the flame and pull on both ends to about 2-3 times its original length. If you pull the
capillary inside the flame, you will have a "piece of art", but not a good spotter. Allow the
capillary to cool down, and then break it in the middle. Make sure that you break off the closed
end on one of them. Do not use gloves when you pull capillaries. You will have much better
control without them! Watch movie how to pull capillaries here here Spotting the plate The
thin end of the spotter is placed in the dilute solution; the solution will rise up in the capillary
(capillary forces). Touch the plate briefly at the start line. Allow the solvent to evaporate and
spot at the same place again. This way you will get a concentrated and small spot. Try to avoid
spotting too much material, because this will deteriorate the quality of the separation
considerably (‘tailing’). The spots should be far enough away from the edges and from each
other as well. If possible, you should spot the compound or mixture together with the starting
materials and possible intermediates on the plate. They will serve as internal reference since
every TLC plate is slightly different. Developing a Plate A TLC plate can be developed in a
beaker or closed jar (see picture below). Place a small amount of solvent (= mobile phase) in the
container. The solvent level has to be below the starting line of the TLC, otherwise the spots will
dissolve away. The lower edge of the plate is then dipped in a solvent. The solvent (eluent)
travels up the matrix by capillarity, moving the components of the samples at various rates
because of their different degrees of interaction with the matrix (=stationary phase) and solubility
in the developing solvent. Non-polar solvents will force non-polar compounds to the top of the
plate, because the compounds dissolve well and do not interact with the polar stationary phase.
Allow the solvent to travel up the plate until ~1 cm from the top. Take the plate out and mark the

2. solvent front immediately. Do not allow the solvent to run over the edge of the plate. Next, let
the solvent evaporate completely. TLC chamber for development e.g. beacher with a lid or a
closed jar after ~5 min after ~10 min after drying Visualization There are various techniques
to visualize the compounds. 1. Sulfuric acid/heat: destructive, leaves charred blots behind 2.
Ceric stain: destructive, leaves a dark blue blot behind for polar compounds 3. Iodine: semi-
destructive, iodine absorbs onto the spots, not permanent 4. UV light: non-destructive, long
wavelength (background green, spots dark), short wavelength (plate dark, compounds glow), Do
not look into the UV lamp!!! Circle the spots on the TLC plate to have a permanent record how
far the compound traveled on the plate. Also draw a sketch of the developed plate in your lab
notebook. Analysis The components, visible as separated spots, are identified by comparing the
distances they have traveled with those of the known reference materials. Measure the distance
of the start line to the solvent front (=d). Then measure the distance of center of the spot to the
start line (=a). Divide the distance the solvent moved by the distance the individual spot moved.
The resulting ratio is called Rf-value. The value should be between 0.0 (spot did not moved from
starting line) and 1.0 (spot moved with solvent front) and is unitless. The Rf (=retardation
factor) depends on the following parameters: solvent system absorbent (grain size, water
content, thickness) amount of material spotted temperature Due to the fact that all those variables
are difficult to keep constant, a reference compound is usually applied to the plate as well.
Solution
last updated Friday, August 14, 2009 Introduction Thin-layer chromatography
(TLC) is a very commonly used technique in synthetic chemistry for identifying compounds,
determining their purity and following the progress of a reaction. It also permits the optimization
of the solvent system for a given separation problem. In comparison with column
chromatography, it only requires small quantities of the compound (~ng) and is much faster as
well. Stationary Phase As stationary phase, a special finely ground matrix (silica gel, alumina,
or similar material) is coated on a glass plate, a metal or a plastic film as a thin layer (~0.25 mm).
In addition a binder like gypsum is mixed into the stationary phase to make it stick better to the
slide. In many cases, a fluorescent powder is mixed into the stationary phase to simplify the
visualization later on (e.g. bright green when you expose it to 254 nm UV light). Preparing the
Plate Do not touch the TLC plate on the side with the white surface. In order to obtain an
imaginary start line, make two notches on each side of the TLC plate. You can also draw a thin
line with pencil. Do not use pen. Why? The start line should be 0.5-1 cm from the bottom of the
plate. Capillary spotters Place a melting point capillary and in the dark blue part of the
Bunsen burner flame. Hold it there until it softens and starts to sag. Quickly remove the capillary
from the flame and pull on both ends to about 2-3 times its original length. If you pull the

3. capillary inside the flame, you will have a "piece of art", but not a good spotter. Allow the
capillary to cool down, and then break it in the middle. Make sure that you break off the closed
end on one of them. Do not use gloves when you pull capillaries. You will have much better
control without them! Watch movie how to pull capillaries here here Spotting the plate The
thin end of the spotter is placed in the dilute solution; the solution will rise up in the capillary
(capillary forces). Touch the plate briefly at the start line. Allow the solvent to evaporate and
spot at the same place again. This way you will get a concentrated and small spot. Try to avoid
spotting too much material, because this will deteriorate the quality of the separation
considerably (‘tailing’). The spots should be far enough away from the edges and from each
other as well. If possible, you should spot the compound or mixture together with the starting
materials and possible intermediates on the plate. They will serve as internal reference since
every TLC plate is slightly different. Developing a Plate A TLC plate can be developed in a
beaker or closed jar (see picture below). Place a small amount of solvent (= mobile phase) in the
container. The solvent level has to be below the starting line of the TLC, otherwise the spots will
dissolve away. The lower edge of the plate is then dipped in a solvent. The solvent (eluent)
travels up the matrix by capillarity, moving the components of the samples at various rates
because of their different degrees of interaction with the matrix (=stationary phase) and solubility
in the developing solvent. Non-polar solvents will force non-polar compounds to the top of the
plate, because the compounds dissolve well and do not interact with the polar stationary phase.
Allow the solvent to travel up the plate until ~1 cm from the top. Take the plate out and mark the
solvent front immediately. Do not allow the solvent to run over the edge of the plate. Next, let
the solvent evaporate completely. TLC chamber for development e.g. beacher with a lid or a
closed jar after ~5 min after ~10 min after drying Visualization There are various techniques
to visualize the compounds. 1. Sulfuric acid/heat: destructive, leaves charred blots behind 2.
Ceric stain: destructive, leaves a dark blue blot behind for polar compounds 3. Iodine: semi-
destructive, iodine absorbs onto the spots, not permanent 4. UV light: non-destructive, long
wavelength (background green, spots dark), short wavelength (plate dark, compounds glow), Do
not look into the UV lamp!!! Circle the spots on the TLC plate to have a permanent record how
far the compound traveled on the plate. Also draw a sketch of the developed plate in your lab
notebook. Analysis The components, visible as separated spots, are identified by comparing the
distances they have traveled with those of the known reference materials. Measure the distance
of the start line to the solvent front (=d). Then measure the distance of center of the spot to the
start line (=a). Divide the distance the solvent moved by the distance the individual spot moved.
The resulting ratio is called Rf-value. The value should be between 0.0 (spot did not moved from
starting line) and 1.0 (spot moved with solvent front) and is unitless. The Rf (=retardation
factor) depends on the following parameters: solvent system absorbent (grain size, water

4. content, thickness) amount of material spotted temperature Due to the fact that all those variables
are difficult to keep constant, a reference compound is usually applied to the plate as well.