Process for eliminating trifluoroacetic acid in coenzyme I
A technology of trifluoroacetic acid and coenzyme, which is applied in the preparation of sugar derivatives, sugar derivatives, sugar derivatives, etc., can solve the problems of high residue and poor removal effect, and achieve a long process, fast moving speed, and easy removal. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0044]Sephadex G25 was mixed with purified water for swelling. A glass column with an inner diameter of 5 cm and a height of 100 cm was used as a chromatography column, and the swollen Sephadex G25 was loaded into the chromatography column, and the Sephadex G25 was filled with a total of 1.6 L. Then the coenzyme I with a volume concentration of 40% is delivered to the chromatography column by a diaphragm pump at a feed rate of 18mL / min for chromatographic separation, and the eluent is delivered to the chromatography column at 8L / h for elution. At the same time, the ultraviolet detector is used to monitor the liquid after chromatographic separation, and the eluate is collected at the same time as the detection. When the reading of the protein nucleic acid meter tends to be stable, the sample can be collected for testing. Wherein, the total feed amount of coenzyme I is 50mL.
Embodiment 2
[0046] Sephadex G25 was mixed with purified water for swelling. A glass column with an inner diameter of 5 cm and a height of 110 cm was used as a chromatography column, and the swollen Sephadex G25 was loaded into the chromatography column, and the Sephadex G25 was filled with a total of 1.5 L. Then the coenzyme I with a volume concentration of 38% is delivered to the chromatography column by a diaphragm pump at a feed rate of 20mL / min for chromatographic separation, and the eluent is delivered to the chromatography column at 8L / h for elution. At the same time, the protein and nucleic acid instrument is used to monitor the liquid after chromatographic separation, and the eluate is collected while detecting. When the reading of the ultraviolet detector tends to be stable, the sample can be collected for testing. Wherein, the total feed amount of coenzyme I is 50mL.
Embodiment 3
[0048] Sephadex G25 was mixed with purified water for swelling. A glass column with an inner diameter of 5 cm and a height of 100 cm was used as a chromatography column, and the swollen Sephadex G25 was loaded into the chromatography column, and the Sephadex G25 was filled with a total of 1.7 L. Then the coenzyme I with a volume concentration of 42% is delivered to the chromatographic column by a diaphragm pump at a feed rate of 16mL / min for chromatographic separation, and the eluent is delivered to the chromatographic column at 7L / h for elution. At the same time, the protein and nucleic acid instrument is used to monitor the liquid after chromatographic separation, and the eluate is collected while detecting. When the reading of the ultraviolet detector tends to be stable, the sample can be collected for testing. Wherein, the total feed amount of coenzyme I is 50mL.
PUM
| Property | Measurement | Unit |
|---|---|---|
| height | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


