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HEPPE MEDICAL CHITOSAN GMBH Chitosan

Chitosan is a nitrogenous polysaccharide. The monomer of chitosan is glucosamine. Chitosans in dissolved form are positively charged. Due to their different degrees of deacetylation and molecular weights, chitosans are a large group of substances with different properties.

Chemical Name: Chitosan

CAS Number: 9012-76-4

Functions: Anti-Fungal Agent, Anti-Inflammatory, Anti-Microbial Agent, Bacteriostatic Agent

Labeling Claims: Non-Toxic

Synonyms: poliglusam

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Identification & Functionality

Chemical Name
Molecular formula
(C₆H₁₁NO₄)ₙ
CAS No.
9012-76-4
EC No.
618-480-0
Chitosan Oligomer

Chitosan oligosaccharide is an oligomer of β-(1 ➔ 4)-linked d-glucosamine. Chitosan oligomer can be prepared from the deacetylation and hydrolysis of chitin.

Chemical Structure

HEPPE MEDICAL CHITOSAN GMBH Chitosan - Chemical Structure

Features & Benefits

Labeling Claims
Properties
  • Biodegradable by enzymes, non-toxic
  • Detected in the human body as an endogenous substance
  • Inhibiting the growth of bacteria and fungi
  • Film- and fiber-forming, cross-linking
  • Anti-inflammatory
  • Haemostatic, wound-healing
  • Odor-absorbing, capable of bonding to proteins, heavy metals, suspended solids
  • Having a stimulating effect on the immune system and metabolism
Properties

 

  • Not thermo-elastic, decomposes at 280° C
  • pKa 6.3
  • High charge carrier density
  • Biodegradable
  • Non-toxic
  • Bacteriostatic
  • Fungistatic
  • Film and fiber forming, cross-linking
  • Immobilization of living organisms
  • Anti-inflammatory, improves wound healing
  • Stimulation of immune system and metabolism
  • Deodorizing
  • Bonding ability to proteins, heavy metals and aerosols

Applications & Uses

Manufacturing Process

In the deacetylation process, chitin is subjected to treatment with concentrated lye to dissociate acetyl groups from the polymer. The result is chitosan that, depending on the degrees of deacetylation and polymerization (chain length), has more or less pronounced properties.

Applications

Cosmetics industry

  • Skin creams - Enhancement of water bonding capacity; bonding of perfume oils; nurturing properties (e.g. neurodermatitis)
  • Hair care - Film formation on hair (protection), thus improving hair elasticity and avoidance of split ends; reduction of electrostatic charging
  • Oral hygiene - Bacteriostatic effect; gel basis for toothpastes; N-carboxy methyl chitosan against periodontitis

Medical Devices

  • Wound and burn treatment, inter alia also with decubitus sores; artificial skin; surgical suture material; haemostatic agent
  • Contact lenses
  • Antibacterial and antifungal agents in formulations
  • Carrier material in tissue engineering
  • Implants
  • Wound care - Accelerated wound healing process, combination of chitosan and chitosan oligomers for wound dressings
  • Drug delivery - Vectors for gene delivery, chitosan oligomer forms complexes with plasmid DNA – drug delivery e.g. to lungs and intestinal epithelium
  • Tissue engineering - Chitosan oligomer promotes differentiation of mesenchymal stem cells to osteoblasts – formation of bone tissue
  • Gene delivery
  • Adjuvant in vaccines
  • Hydrogels
  • Antibacterial effects

Pharmaceutics

  • Excipient:
    • Improvement of releasing properties of active substances (controlled release and drug delivery systems for the following intake routes: oral, pulmonary, parenteral, nasal, ocular, transdermal),
    • As a filler in tablets,
    • As a hydrogel to increase viscosity of solutions.
  • Active substance: in gene and tumor therapies in the form of chitosan derivatives.
Derivatives

Chitin and chitosan derivatives are extremely versatile. Most of them are directly soluble in water and, depending on their derivatisation, can be applied in neutral and basic pH ranges. Thus, the derivatives have very comprehensive and customized potential applications. Our standard derivatives include:

  • Chitosan HCl
  • N, O-Carboxymethyl-Chitosan (CMC)
  • Chitosan Lactate
  • Chitosan Acetate
  • Chitosan Glutamate
Production Process

Chitosan differs from chitin in that it has free amino groups (figure 1) and is obtained by deacetylizing chitin. At a minimum deacetylization level of 70% (=amount of free amino groups in the polymer) it is considered to be chitosan. The monomer of chitosan is D-amino glucose.

Properties

Appearance
White to Light Yellow (Solid), Clear, Colorless to Slightly Yellowish (Solution)
Insoluble in
Water, Sulphuric Acid
Soluble in
Diluted Acids (pH - max. 6)
Typical Properties
ValueUnitsTest Method / Conditions
Dry matter contentmin. 85%HMC QK-PA-0006
Degree of Deacetylation80 - 95%HMC QK-PA-0014
Viscosity (1% in Acetic Acid, 20°C)min. 5mPasHMC QK-PA-0004
pH (1% in Water, 20°C)3 - 7HMC QK-PA-0013
Ash Content (Sulphated)max. 1%HMC QK-PA-0005
Insolublesmax. 2%HMC QK-PA-0010
Molecular Weightapprox. 30 - 200kDa
Protein contentmax. 0.5%
Microbiological Values
ValueUnitsTest Method / Conditions
Total Bacterial Countmax. 1000cfu/gHMC QK-PA-0022
Heavy Metals
ValueUnitsTest Method / Conditions
Mercury Contentmax. 0.2ppmHMC QK-PA-0020
Cadmium Contentmax. 0.5ppmHMC QK-PA-0020
Lead Contentmax. 40ppmHMC QK-PA-0019
Arsenic Contentmax. 0.5ppmHMC QK-PA-0020

Storage & Handling

Shelf Life
36 Months