C08B37/00

GREEN CATIONIZATION AGENT
20220403055 · 2022-12-22 ·

A compound having Formula (I) or Formula (II):

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or a mixture thereof,

in which R is —H; —CH.sub.3; —CH—(CH.sub.3).sub.2; —CH.sub.2—CH—(CH.sub.3).sub.2; —CH—(CH.sub.3)—CH.sub.2—CH.sub.3; —CH.sub.2—(C.sub.6H.sub.5); —CH.sub.2—(3-indole); —CH.sub.2—CH.sub.2—S—CH.sub.3; —CH.sub.2—OH; —CH—(CH.sub.3)—OH; —CH.sub.2—SH; —CH.sub.2-(p-C.sub.6H.sub.40H); —CH.sub.2—CH.sub.2—CH.sub.2—CH.sub.2—NH.sub.2; —CH.sub.2—CO—NH.sub.2; —CH.sub.2—CH.sub.2—CO—NH.sub.2; —CH.sub.2—CH.sub.2—COOH; —CH.sub.2—COOH; or —CH.sub.2—CH.sub.2—NH—C═NH.sub.2(NH.sub.2);

and X is a suitable non-interfering anion, a process for making the compound having Formula (I) or Formula (II), and a process for reacting the compound having Formula (I) or Formula (II) or a mixture thereof with a (poly)saccharide to form a cationized (poly)saccharide.

NOVEL CROSSLINKED ALGINIC ACID STRUCTURE

Provided are a novel crosslinked alginic acid, a crosslinked alginic acid structure, etc., by performing a crosslinking reaction using alginic acid derivatives represented by formula (I) and formula (II). As a result, a novel crosslinked alginic acid, crosslinked alginic acid structure, etc., are provided.

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METHOD FOR PRODUCING WATER-SOLUBLE POLYSACCHARIDES

[Problem] An object is to obtain a water-soluble polysaccharide (mainly pectin) in a high yield under mild extraction conditions (temperature and pH) and also without using any special agent or extraction device, and to suppress the excessive degradation of the polysaccharide (reduction in the molecular weight of a neutral sugar side chain, demethyl esterification, and deacetylation).

[Means for Solution] By adjusting the particle size of pulp dried with superheated steam of the beet pulp generated as a by-product in a step of producing sugar from sugar beet and using the resultant as a raw material, a water-soluble polysaccharide (mainly pectin) can be obtained in a high yield in a short time under mild extraction conditions, and also the excessive degradation of the water-soluble polysaccharide (reduction in the molecular weight of a neutral sugar side chain, demethyl esterification, and deacetylation) can be suppressed.

PURIFICATION OF SULFOBUTYLATED CYCLODEXTRINS WITH SPECIFIC ION EXCHANGE RESINS

Present invention relates to a process to reduce butane sultone hydrolysis products (4-hydroxybutane-1-sulfonic acid, and bis(4-sulfobutyl) ether disodium) in sulfobutylether cyclodextrin reaction mixtures achieved with the combined use of a strong anion exchange resin having dialkyl 2-hydroxyethyl ammonium hydroxide functionality and a cation exchange resin.

Compositions comprising glucose and hemicellulose and their use

Provided herein are purified hemicellulose compositions, sweetener compositions including purified hemicellulose compositions, as well as methods for making the same. Also provided are uses of the compositions.

METHOD OF PROCESSING SEAWEED
20220389124 · 2022-12-08 ·

The present invention relates to a method of processing macroalgae in which superheated water is used in an initial pre-treatment step prior to extraction of a polysaccharide. In particular, the invention relates to a process for obtaining polysaccharide (e.g. alginate) from macroalgae or a part thereof. Certain aspects of the invention relate to a process for obtaining polysaccharide from macroalgae which results in enhanced polysaccharide yield and/or a shortened treatment time when compared to conventional extraction methods.

AMINE-FUNCTIONALIZED SACCHARIDE POLYMERS PREPARED BY HYPOCHLORITE OXIDATION

Amine-functionalized saccharide polymers, including oligosaccharides and polysaccharides, may be effective for promoting clay stabilization in subterranean formations. Oxidative synthesis of amine-functionalized saccharide polymers using sodium hypochlorite pentahydrate as an oxidation reagent may afford a different distribution and type of sites of oxidative opening as compared to other types of oxidation reagents. Amine-functionalized saccharide polymers may be prepared by exposing a saccharide polymer comprising a trans-vicinal diol to an oxidation reagent comprising sodium hypochlorite pentahydrate, reacting the trans-vicinal diol to form a site of oxidative opening bearing at least one aldehyde, exposing the at least one aldehyde to an amine to form an imine intermediate at the site of oxidative opening, and reducing the imine intermediate into a secondary or tertiary amine at the site of oxidative opening.

Method for Extracting Polysaccharides

Provided herein is a method for extracting polysaccharides, for example, β-glucan and sodium alginate, from a sample including a botanical product. The extraction can be carried out using a microwave assisted dual-solvent extraction followed by one or more membrane filtration steps.

METHOD FOR PRODUCING HEPARIN-LIKE SUBSTANCE, RECOMBINANT CELL, AND METHOD FOR PRODUCING THE SAME

An object of the present invention is to provide a method for efficiently producing a heparin-like substance without using an animal-derived tissue. The present invention relates to a method for producing a heparin-like substance and the like, the method comprising: (1) preparing a mammalian cell that produces a heparin-like substance, (2) preparing a recombinant cell in which a gene that encodes an extracellular domain of syndecan is introduced into the mammalian cell that produces a heparin-like substance and is prepared in step (1), and (3) culturing the recombinant cell prepared in step (2) in a medium and collecting the heparin-like substance from the resulting culture supernatant.

Method for preparing porous scaffold for tissue engineering, cell culture and cell delivery

The present invention relates to a method for preparing a porous scaffold for tissue engineering. It is another object of the present invention to provide a porous scaffold obtainable by the method as above described, and its use for tissue engineering, cell culture and cell delivery. The method of the invention comprises the steps consisting of: a) preparing an alkaline aqueous solution comprising an amount of at least one polysaccharide, an amount of a cross-linking agent and an amount of a porogen agent b) transforming the solution into a hydrogel by placing said solution at a temperature from about 4° C. to about 80° C. for a sufficient time to allow the cross-linking of said amount of polysaccharide and c) submerging said hydrogel into an aqueous solution d) washing the porous scaffold obtained at step c).