| Brand |
Eata Marisource |
| Product Grade |
High Purity / Biomedical Feedstock |
| Chemical Name |
Chitin (poly-N-acetylglucosamine) |
| Molecular Formula |
(C8H13NO5)n |
| Molecular Weight |
Grade-dependent |
| Raw Material Source |
Crustacean shell |
| Physical Form |
Flake or powder |
| Appearance |
Slightly yellow |
| Odor |
Odorless |
| Solubility |
Soluble in 8% LiCl/DMAc and concentrated acids; insoluble in water, dilute acid, alkali, ethanol and common organics |
| Moisture (Loss on Drying) |
≤10.0% |
| Ash Content |
≤2.0% |
| Intended Use |
Chitosan conversion feedstock, biomedical materials, industrial and agricultural applications |
| Target Industries |
Biomedical, textiles, water treatment, agriculture, cosmetics |
| Recommended Applications |
Precursor to fibers, films, sutures, dialysis membranes and vascular grafts; insecticide and antiviral agro bases; cosmetic moisturizer feedstock |
| Recommended Use Level |
Feedstock dosing per conversion route |
| Appearance of Solution |
Dissolve in LiCl/DMAc or concentrated acid media under controlled temperature |
| Handling & Safety |
Keep dry; avoid strong oxidizers |
| Chemical Class |
Acetylated aminopolysaccharide |
| Structural Unit |
β-(1→4)-linked N-acetyl-D-glucosamine |
| Functional Groups |
Acetamido and hydroxyl groups |
| Ionic Character |
Neutral polymer |
| Key Features |
Protein ≤3.0%; ash ≤2.0%; defined solvent routes for regeneration and spinning |
| Functional Benefits |
Low residual protein supports biomedical conversion; the classic gateway polymer to chitosan and chitin nanomaterials |
| Mechanism of Action |
Acetamido backbone provides structural rigidity; dissolution routes regenerate chitin into fibers, films and scaffolds |
| Typical End Products |
Contact lenses, artificial skin, sutures, dialysis membranes, vascular grafts, specialty textiles |
| Formulation Compatibility |
Processing via LiCl/DMAc, ionic liquids or acid media per downstream design |
| Preparation & Dissolution Guidance |
Dry before dissolution; control acid exposure time to protect chain length |
| Reactivity & Derivatization |
Acetamido groups hydrolyze toward chitosan; hydroxyls support esterification |
| Stability Notes |
Very stable as dry flake; inert across wide pH in solid state |
| Usage Precautions |
Solvent dissolution involves hazardous media: industrial controls required |
| Environmental Profile |
Marine by-product valorization at industrial scale |
| Analytical Methods |
Protein; ash; moisture; acetylation degree; solvent-solubility check |