Production of water-soluble chitin-oligomers by partial hydrolysis of chitin

Claim 2

A process for the production of tetra-N-acetylchitotetraose, penta-N-acetyl-chitopentaose and hexa-N-acetyl-chitohexaose, these chitin-oligomers being represented by the general formula (I) ##STR4## wherein n is 2 for the tetra-N-acetyl-chitotetraose, n is 3 for the penta-N-acetyl-chitopentaose, and n is 4 for the hexa-N-acetyl-chitohexaose, which comprises adding finely ground chitin at once to and intimately mixing said chitin with an amount of a concentrated hydrohalogenic acid containing 1.5 mol to 6 mol of the hydrogen halide per 100 g of the chitin initially charged, while being irradiated with ultrasonic waves and also agitated by means of mechanical stirrer, to form a homogeneous mixture of the fine chitin particles with the concentrated hydrohalogenic acid, and then hydrolyzing the chitin with the concentrated hydrohalogenic acid, while the resulting homogeneous reaction mixture comprising the chitin and the concentrated hydrohalogenic acid is further continuously irradiated with the ultrasonic waves and also agitated by means of the mechanical stirrer.

Claim 3

A process as claimed in claim 1, for the production of tetra-N-acetyl-chitotetraose, penta-N-acetyl-chitopentaose and hexa-N-acetyl-chitohexaose, which comprises the steps of: (i) adding finely ground chitin at once to and intimately mixing said chitin with an amount of a concentrated hydrohalogenic acid containing 1.5 mol to 6 mol of the hydrogen halide per 100 g of the chitin initially charged, while being irradiated with ultrasonic waves and also agitated by means of mechanical stirrer, to form a homogeneous mixture of the fine chitin particles with the concentrated hydrohalogenic acid, (ii) then hydrolyzing the chitin with the concentrated hydrohalogenic acid, while the resulting homogeneous reaction mixture comprising the chitin and the concentrated hydrohalogenic acid is further continuously irradiated with the ultrasonic waves and also agitated by means of the mechanical stirrer, (iii) continuing the reaction of hydrolyzing the chitin under the irradiation with the ultrasonic waves and under the agitation by the mechanical stirrer, until 40% by weight or more of the chitin charged have been depolymerized hydrolytically and dissolved into the aqueous phase of the reaction mixture, with formation of N-acetylglucosamine, di-N-acetyl-chitobiose, tri-N-acetyl-chitotriose, tetra-N-acetyl-chitotetraose, penta-N-acetyl-chitopentaose, hexa-N-acetyl-chitohexaose and hepta-N-acetyl-chitoheptaose which are soluble in water, and (iv) recovering from the aqueous phase of the hydrolyzed reaction mixture the desired tetra-N-acetyl-chitotetraose, penta-N-acetyl-chitopentaose and hexa-N-acetyl-chitohexaose, either in mixture or singly.

Claim 4

A process as claimed in claim 1 or 2, in which the hydrohalogenic acid used is a 10N to 12N hydrochloric acid and the chitin is hydrolyzed with a concentrated hydrochloric acid containing the hydrogen chloride at a concentration of 10N to 12N at a temperature of 35° C. to 40° C. for a time of about 2 hours to 3 hours.

Claim 5

A process as claimed in claim 1 or 2, in which the mixture comprising the chitin and the concentrated hydrochloric acid is continuously irradiated with ultrasonic waves of frequencies of 10 K Hz to 200 K Hz and also agitated by mechanical stirrer.

Claim 6

A process as claimed in claim 1 or 2, in which the reaction of hydrolyzing the chitin is effected under the irradiation with ultrasonic waves and under the mechanical agitation by stirrer until 40% to 80% by weight of the chitin initially charged have been depolymerized hydrolytically and dissolved in the aqueous phase of the reaction mixture.

Claim 7

A process as claimed in claim 2, in which the acid used is a concentrated hydrochloric acid and the step of recovering the tetra-N-acetyl-chitotetraose, penta-N-acetyl-chitopentaose and hexa-N-acetylhexaose from the aqueous phase of the hydrolyzed reaction mixture includes stages where (a) the whole, hydrolyzed reaction mixture after the completed reaction is neutralized with aqueous sodium or potassium hydroxide, aqueous sodium or potassium carbonate or aqueous sodium or potassium hydrogen carbonate, (b) the neutralized reaction mixture is filtered to remove the insoluble residue and afford the neutral, aqueous filtrate containing N-acetylglucosamine, the water-soluble chitin-oligomers and the sodium chloride as formed, (c) the neutral aqueous filtrate obtained is then desalted, (d) the resulting de-salted aqueous solution containing the N-acetylglucosamine and the water-soluble chitin-oligomers is concentrated or dried to give a concentrate or solid mixture containing the N-acetylglucosamine and the chitin-oligomers, and (e) the concentrate or solid mixture so obtained is chromatographed on a column of a gel-filtration agent or by a high pressure liquid chromatography, to obtain the tetra-N-acetyl-chitotetraose, penta-N-acetylchitopentaose and hexa-N-acetyl-chitohexaose, either in mixture or singly.