Carboxymethylation lentinan, synthesis and purification method and application of carboxymethylation lentinan serving as tobacco humectant
A carboxymethylated shiitake mushroom and humectant technology, which is applied in the application of tobacco humectant, carboxymethylated lentinan, synthesis and purification fields, has achieved significant industrial application value, broad promotion and application prospects, and obvious moisturizing effect Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] A synthesis and purification method of carboxymethylated lentinan, comprising the following steps: adding 14.0g NaOH and 120mL solvent (ionic liquid / water=1.4:1, mass ratio) into a three-necked flask, stirring at room temperature until the solution is clear, adding Stir 10g of lentinan vigorously for 20min until fully dissolved, then slowly add 16.0g of chloroacetic acid, stir and react at 60°C for 3.5h, cool to room temperature, adjust the pH to 7 with dilute acetic acid, precipitate with alcohol, filter, and collect the precipitate.
[0023] The precipitate was dissolved with an appropriate amount of water, precipitated with 3 times the volume of 95% ethanol, and centrifuged at 4000r / m for 20min. The precipitate was collected again and dialyzed against running water using a dialysis bag. First dialyze with tap water for 24 hours, then dialyze with distilled water for 24 hours, and finally freeze-dry to obtain white cotton-like carboxymethylated mushroom crude polysacc...
Embodiment 2
[0026] A method for synthesizing and purifying carboxymethylated lentinan, comprising the following steps: adding 16.0g NaOH and 120mL solvent (ionic liquid / water=1.4:1, mass ratio) to a three-necked flask, stirring at room temperature until the solution is clear, adding Stir 10g of lentinan vigorously for 30min until fully dissolved, then slowly add 16.4g of chloroacetic acid, stir and react at 70°C for 4h, cool to room temperature, adjust the pH to 7 with dilute acetic acid, precipitate with alcohol, filter, and collect the precipitate.
[0027] The precipitate was dissolved with an appropriate amount of water, precipitated with 3 times the volume of 95% ethanol, and centrifuged at 4000r / m for 20min. The precipitate was collected again and dialyzed against running water using a dialysis bag. First dialyze with tap water for 24 hours, then dialyze with distilled water for 24 hours, and finally freeze-dry to obtain white cotton-like carboxymethylated mushroom crude polysacchar...
Embodiment 3
[0030] A synthesis and purification method of carboxymethylated lentinan, comprising the following steps: adding 18.0g NaOH and 120mL solvent (ionic liquid / water=1.4:1, mass ratio) to a three-necked flask, stirring at room temperature until the solution is clear, adding Stir 10g of lentinan vigorously for 30min until fully dissolved, then slowly add 16.8g of chloroacetic acid, stir and react at 80°C for 4.5h, cool to room temperature, adjust the pH to 7 with dilute acetic acid, precipitate with alcohol, filter, and collect the precipitate.
[0031] The precipitate was dissolved with an appropriate amount of water, precipitated with 3 times the volume of 95% ethanol, and centrifuged at 4000r / m for 20min. The precipitate was collected again and dialyzed against running water using a dialysis bag. First dialyze with tap water for 24 hours, then dialyze with distilled water for 24 hours, and finally freeze-dry to obtain white cotton-like carboxymethylated mushroom crude polysaccha...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com