C08B11/145

METHOD OF PREPARING A SILICON GLYCAN
20220363783 · 2022-11-17 ·

A method for preparing a silicon glycan is provided. The method includes reacting (A) a polysaccharide and (B) an anhydride-functional organosilicon compound, to give the silicon glycan. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and linking moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with substituted or unsubstituted hydrocarbyl groups, ether moieties, and/or amine moieties.

METHOD OF PREPARING A SILICON GLYCAN
20220363783 · 2022-11-17 ·

A method for preparing a silicon glycan is provided. The method includes reacting (A) a polysaccharide and (B) an anhydride-functional organosilicon compound, to give the silicon glycan. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and linking moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with substituted or unsubstituted hydrocarbyl groups, ether moieties, and/or amine moieties.

SILICON GLYCAN AND METHOD OF PREPARING SAME
20220356270 · 2022-11-10 ·

A silicon glycan is provided. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and amide moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with substituted or unsubstituted hydrocarbyl groups, ether moieties, and/or amine moieties. A method of preparing the silicon glycan is also provided. The method includes reacting (A) an aminoethyl polysaccharide and (B) an anhydride-functional organosilicon compound, to give the silicon glycan. The method may include preparing the aminoethyl polysaccharide (A) by reacting (A1) a hydroxyl-functional polysaccharide and (A2) an aziridinium halide compound to give the aminoethyl polysaccharide (A).

SILICON GLYCAN AND METHOD OF PREPARING SAME
20220356270 · 2022-11-10 ·

A silicon glycan is provided. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and amide moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with substituted or unsubstituted hydrocarbyl groups, ether moieties, and/or amine moieties. A method of preparing the silicon glycan is also provided. The method includes reacting (A) an aminoethyl polysaccharide and (B) an anhydride-functional organosilicon compound, to give the silicon glycan. The method may include preparing the aminoethyl polysaccharide (A) by reacting (A1) a hydroxyl-functional polysaccharide and (A2) an aziridinium halide compound to give the aminoethyl polysaccharide (A).

CARRIER FOR ENZYME IMMOBILIZATION USE, AND IMMOBILIZED ENZYME

This invention provides a novel carrier for enzyme immobilization and an immobilized enzyme. The carrier for enzyme immobilization according to an embodiment comprises a porous material and cellulose that has an amino group-containing substituent at an anomeric position and is immobilized on the porous material. The immobilized enzyme contains the carrier for enzyme immobilization and an enzyme immobilization on the cellulose. The carrier for enzyme immobilization is obtained by adding an acid to an aqueous solution in which cellulose having an amino group-containing substituent at an anomeric position is dissolved in an aqueous alkaline solution to deposit the cellulose in the presence of a porous material. The immobilized enzyme is obtained by immobilizing an enzyme on the cellulose.

Cellulose ethers substituted with hydroxyl and alkyne groups and with hydroxyalkyl, alkyne and azide groups, and use thereof as water-insoluble adhesives
20170253674 · 2017-09-07 ·

Nonionic, water-soluble cellulose ethers are disclosed with hydroxyalkyl groups and ω-alkynyl groups, each joined to the cellulose via an ether bond, the degree of molar substitution MS(alkyne) being in the range from 0.001 to 0.30. The cellulose ethers may further contain azido groups, preferably 3-azido-2-hydroxypropyl groups, likewise joined to the cellulose by an ether bond, the MS(AHP) being in the range from 0.001 to 0.3. To obtain an adhesive, cellulose ether is mixed with water or. if the cellulose ether contains no alkyne groups, is mixed additionally with a non-ionic cellulose ether containing ω-alkyne groups and hydroxyalkyl groups, each bonded to the cellulose by ether bonds. The mixture is applied to at least one of the surfaces to be bonded and then is contacted with a copper(I) catalyst or a ruthenium catalyst. The adhesive is especially suitable for bonding wood, paper, cardboard or other cellulosic material.

Fabric treatment composition

The present invention relates to a fabric treatment composition capable of enhancing cleaning properties of a soil during cleaning through treatment of a fabric to be treated and a method for treating a fabric with the fabric treatment composition. The fabric treatment composition is a fabric treatment composition containing a hydroxyalkyl cellulose (A) in which a hydroxyalkyl cellulose is bound to at least one selected from a cationic group and a hydrophobic group including a hydrocarbon group having 4 or more carbon atoms, the content of a surfactant (B) being 3.5 parts by mass or less relative to 1 part by mass of the hydroxyalkyl cellulose (A).

Composition

The present invention relates a composition capable of enhancing cleaning properties of a soil during cleaning by treating an object. The composition is a composition containing a modified hydroxyalkyl cellulose and at least one selected from an anionic surfactant and a nonionic surfactant, the modified hydroxyalkyl cellulose being one in which a cationic group and a hydrophobic group represented by the formula (1) are bound to a group resulting from eliminating a hydrogen atom from a hydroxy group of a hydroxyalkyl cellulose.
*—Z—R.sup.1  (1)
wherein, Z represents a single bond or a hydrocarbon group having an oxygen atom; R.sup.1 represents a hydrocarbon group having 2 or more carbon atoms; and * represents a binding position to a group resulting from eliminating a hydrogen atom from a hydroxy group of a hydroxyalkyl cellulose.

Polysaccharide derivative

The present invention relates to a polysaccharide derivative which is able to not only enhance cleaning properties of clothing, etc. but also suppress resoiling due to powder soil during washing. The polysaccharide derivative is a polysaccharide derivative having a cationic group and a hydrocarbon group (R) having 2 or more carbon atoms, wherein the hydrocarbon group (R) is bound to a group resulting from eliminating a hydrogen atom from a hydroxy group of a hydroxyalkylated polysaccharide, directly or via a hydrocarbon group having an oxygen atom; the hydroxyalkylated polysaccharide is a hydroxyethylated polysaccharide or a hydroxypropylated polysaccharide; and the hydroxyalkylated polysaccharide has a weight average molecular weight of 10,000 or more and 740,000 or less.

Polysaccharide derivative

The present invention relates to a polysaccharide derivative which is able to not only enhance cleaning properties of clothing, etc. but also suppress resoiling due to powder soil during washing. The polysaccharide derivative is a polysaccharide derivative having a cationic group and a hydrocarbon group (R) having 2 or more carbon atoms, wherein the hydrocarbon group (R) is bound to a group resulting from eliminating a hydrogen atom from a hydroxy group of a hydroxyalkylated polysaccharide, directly or via a hydrocarbon group having an oxygen atom; the hydroxyalkylated polysaccharide is a hydroxyethylated polysaccharide or a hydroxypropylated polysaccharide; and the hydroxyalkylated polysaccharide has a weight average molecular weight of 10,000 or more and 740,000 or less.