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1 vote
1 answer
127 views

Making an UV inactive salt UV active during purification of charged anion with HILIC purification?

In the context of a purification setup I am asking myself the question: Can a UV inactive charged substance made be UV active by a counter ion that absorbs UV light during a column run? If so, when no ...
raptorlane's user avatar
2 votes
0 answers
80 views

When is chromatography regarded as a viable industrial purification strategy?

I understand the basics that chromatography is a fairly slow and expensive process compared to direct synthesis. When a synthesis route is not feasible, the economics become favorable. Not being in ...
ericnutsch's user avatar
2 votes
0 answers
64 views

Mixture is eluted too early from alumina in flash column chromatography

I have recently tried to purify my reaction mixture by column chromatography. Because my reaction mixture had poor resolution in silica-based TLC, I used neutral alumina-based TLC plate. After I ...
Krang Lee's user avatar
  • 1,101
1 vote
0 answers
385 views

Activating alumina before column chromatography

Recently I synthesized some amine compounds, and because it showed better separation in the neutral alumina TLC plates than silica plates, I am planning to purify the reaction mixture using neutral ...
Krang Lee's user avatar
  • 1,101
1 vote
0 answers
84 views

Fragmentation behavior of spots in TLC

I tested multiple development using eluent condition hexane + 1% of ethyl acetate. Then I observed kind of fragmentation of spot. I'm not sure, but I guess that successive spots are from the skyblue ...
Krang Lee's user avatar
  • 1,101
2 votes
0 answers
809 views

Using neutral or basic alumina in column chromatography for purification of amines

I am conducting a synthesis involving amines, and it is found that some spots still hardly moves from the starting point in spite of the dichloromethane 9:methanol 1 eluent condition. Addition of ...
Krang Lee's user avatar
  • 1,101
1 vote
0 answers
19 views

How can I determine the purity of an oligonucleotide solution?

After desalting an oligonucleotide via gel chromatography, I am left with (presumably) an oligonucleotide substance suspended in a buffer. What is the simplest way to verify the oligonucleotide's ...
RecyclingBen's user avatar
2 votes
0 answers
314 views

Analysis of reaction mixture by TLC and finding column chromatography condition

I am conducting an organic synthesis. Below is the TLC image. I used dichloromethane:methanol:triethylamine=10:1:0.15 as eluent, but I stored it during 3 days, so it may be a little bit concentrated. ...
Krang Lee's user avatar
  • 1,101
0 votes
1 answer
124 views

Is it possible to functionalize silica gel as Activated Carbon can be? How?

Activated carbon and Silica gel both have a high surface area. If I understand correctly it is possible to trap stuff inside activated charcoal pores to give it specific retention properties (by ...
Hans's user avatar
  • 1,097
5 votes
1 answer
314 views

Purification of primary amines using Schiff base immobilization

I want to purify all primary amines containing compounds in a complex mixture (cell-extracted metabolites). I'm unaware of any published methods to do so. So I am thinking of making my own using a ...
Kristian Davidsen's user avatar
1 vote
2 answers
1k views

Can separated and purified substances be obtained from a chromatogram?

I am studying chemistry, and I am learning about chromatography. But I am confused about how chromatography is used to ‘separate and purify’ substances. I have learnt about chromatography paper, ...
bzr's user avatar
  • 693
2 votes
1 answer
194 views

Can we use HPLC to purify an organic reaction product?

I know HPLC is a form of column chromatography that uses high pressure to pump a sample mixture/eluent through a column. However, I'm not sure if this technique is being used to purify and isolate ...
harry86's user avatar
  • 23
1 vote
0 answers
54 views

Change buffer in dialysis?

I have a protein that I purified in PBS buffer, pH 7. I will do dialysis to remove salt and will then further purify the protein with ion exchange chromatography. I will need to use another buffer (...
Yana's user avatar
  • 11
1 vote
1 answer
1k views

In HPLC, how does column diameter affect the retention time?

I am using a smaller diameter column than my previous one keeping all other factors such as stationary phase, solvent, solvent gradient constant. (Obviously, flow rate will be less in smaller column). ...
Science123's user avatar
3 votes
0 answers
1k views

Purification of polar NHS esters

What are the options that I might be missing for the purification of a molecule with the following characteristic: Contains an activated ester that reacts with water (NHS) Reacts readily with ...
user46680's user avatar
  • 313

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