GB746870A - Preparation of sulphated chitosan - Google Patents

Preparation of sulphated chitosan

Info

Publication number
GB746870A
GB746870A GB28016/53A GB2801653A GB746870A GB 746870 A GB746870 A GB 746870A GB 28016/53 A GB28016/53 A GB 28016/53A GB 2801653 A GB2801653 A GB 2801653A GB 746870 A GB746870 A GB 746870A
Authority
GB
United Kingdom
Prior art keywords
chitosan
sulphated
salt
filtering
reaction mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB28016/53A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Upjohn Co filed Critical Upjohn Co
Publication of GB746870A publication Critical patent/GB746870A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0024Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
    • C08B37/00272-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
    • C08B37/003Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The invention comprises (1) sulphated chitosan (preferably having a sulphur content of 5 to 23.9 per cent); (2) a salt of sulphated chitosan (preferably having a sulphur content of up to 20.6 per cent); and (3) the preparation of sulphated chitosan by treating chitosan with a sulphating agent, followed, if desired, by neutralizing the reaction mixture to give the corresponding salt. Sulphating agents are preferably fuming sulphuric acid, chlorosulphonic acid (e.g. in pyridine), or a mixture of sulphur dioxide and sulphur trioxide (preferably in a ratio between 1:1 and 30:1). The sulphur dioxide/trioxide treatment is preferably conducted at temperatures below 40 DEG C., in particular between 0 DEG and - 10 DEG C., and for a period of 10 to 24 hours. The sulphated chitosan or salts thereof may be isolated by filtering the reaction mixture or neutralized reaction mixture, washing the precipitate with an organic solvent, suspending the washed precipitate in water, filtering the suspension to remove unreacted chitosan, dialyzing the filtrate, and lyophilizing the dialyzed product. Salts of sulphated chitosan may also be prepared by subsequent conversion of the barium salt, or by treating the suspension of chitosan sulphate in water with, for example, an alkali, filtering, dialyzing, and precipitating the salt with acetone or alcohol, or by evaporating the dialyzed filtrate to dryness. The preparation of the sodium, potassium, calcium, pyridinium and quinolium salts of sulphated chitosan is described.
GB28016/53A 1952-10-15 1953-10-12 Preparation of sulphated chitosan Expired GB746870A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US746870XA 1952-10-15 1952-10-15

Publications (1)

Publication Number Publication Date
GB746870A true GB746870A (en) 1956-03-21

Family

ID=22121045

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28016/53A Expired GB746870A (en) 1952-10-15 1953-10-12 Preparation of sulphated chitosan

Country Status (1)

Country Link
GB (1) GB746870A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0194497A2 (en) * 1985-03-14 1986-09-17 Etablissement Texcontor Chitosan derivatives in the form of coordinated complexes with ferrous ions
FR2744930A1 (en) * 1996-02-15 1997-08-22 Commissariat Energie Atomique PROCESS FOR SEPARATING AT LEAST ONE METAL PRESENT IN A SOLUTION BY FIXING ON A CHITOSAN

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0194497A2 (en) * 1985-03-14 1986-09-17 Etablissement Texcontor Chitosan derivatives in the form of coordinated complexes with ferrous ions
EP0194497A3 (en) * 1985-03-14 1988-03-16 Etablissement Texcontor Chitosan derivatives in the form of coordinated complexes with ferrous ions
US4810695A (en) * 1985-03-14 1989-03-07 Establissement Texcontor Chitosan derivatives in the form of coordinated complexes with ferrous ions
FR2744930A1 (en) * 1996-02-15 1997-08-22 Commissariat Energie Atomique PROCESS FOR SEPARATING AT LEAST ONE METAL PRESENT IN A SOLUTION BY FIXING ON A CHITOSAN
US5932107A (en) * 1996-02-15 1999-08-03 Commissariat A L'energie Atomique Method of separating at least one metal present in a solution by fixation onto a chitosane

Similar Documents

Publication Publication Date Title
GB746870A (en) Preparation of sulphated chitosan
GB603571A (en) Compounds having a retarding action on the coagulation of blood and processes of preparing the same
US4855416A (en) Method for the manufacture of dextran sulfate and salts thereof
JPH0643446B2 (en) Chitosan 6-sulfate and process for producing the same
US2597723A (en) Equilin-3-monosulfate and alkaline salts thereof
US2099214A (en) Process fob forming the sulphuric
US2689850A (en) Method of producing somjble
SU334840A1 (en) The method of obtaining the displaced sulfate-containing cellulose ethers
US1564239A (en) Production and isolation of alkali salts of aromatic sulphonic acids
US3027363A (en) Selective sulfation of amino alcohols and products thereof
US1412949A (en) Manufacture of soluble condensation products
SU95452A1 (en) The method of obtaining highly basic tetravalent titanium sulfates
US2830079A (en) Mixed salts of 3, 4, 5, 6-tetraiodophthalic acid opaque to x-radiation
GB740152A (en) Sulfate esters of partially degraded chitin and salts thereof
SU84A1 (en) The method of preparation of protective sulphurous dye
GB1452844A (en) Process for producing salts of l-asorbic acid-2-sulphate
US1573385A (en) Treatment of earthy minerals
US1674362A (en) Complex antimony compound
GB796477A (en) New anticoagulant and a method of preparing same
SU141151A1 (en) The method of preparation of the sulfochlorination mixture
EP0289894A1 (en) Process for the preparation of L-ascorbic acid derivatives
GB391747A (en) Manufacture of aminothiophenols or substitution products thereof
GB704516A (en) A blood anticoagulating agent and process for the manufacture thereof
GB646258A (en) Improvements in and relating to the preparation and purification of antibiotics
GB174700A (en) Improvements in tanning