American Chemical Suppliers

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Product
Chitinovorin A Chitinovorin A is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Molecular formula: C26H41N9O11S. Mole weight: 687.73. BOC Sciences 12
Chitinovorin B Chitinovorin B is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Synonyms: L-Alaninamide, L-alanyl-N-(4-((7-((5-amino-5-carboxy-1-oxopentyl)amino)-2-carboxy-7-(formylamino)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methoxy)-1-(3-((aminoiminomethyl)amino)propyl)-2-hydroxy-4-oxobutyl)-, (6R-(3(1S*,2R*),6alpha,7beta(R*)))-. Grade: >98%. CAS No. 95722-76-2. Molecular formula: C29H46N10O12S. Mole weight: 758.80. BOC Sciences 12
Chitinovorin C Chitinovorin C is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. It has weak anti-gram-negative bacterial activity. Synonyms: 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-((5-amino-5-carboxy-1-oxopentyl)amino)-7-(formylamino)-3-(hydroxymethyl)-8-oxo-, (6R-(6alpha,7beta(R*)))-; 7-[(5-Amino-5-carboxy-1-hydroxypentylidene)amino]-3-(hydroxymethyl)-7-[(hydroxymethylidene)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 95230-98-1. Molecular formula: C15H20N4O8S. Mole weight: 416.41. BOC Sciences 12
Chitin (Plant-Based) - C-M-112 Chitin (Plant-Based). Source: Mushroom. ChitoLytic
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chitin synthase Converts UDP-N-acetyl-α-D-glucosamine into chitin and UDP. Group: Enzymes. Synonyms: chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Enzyme Commission Number: EC 2.4.1.16. CAS No. 9030-18-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2384; chitin synthase; EC 2.4.1.16; 9030-18-6; chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Cat No: EXWM-2384. Creative Enzymes
Chitobiose Chitobiose is a highly significant compound extensively employed in the compound sector, serving as a fundamental component facilitating chitosan research, an environmentally friendly polymer derived from crustacean exoskeletons. With its pivotal involvement, Chitobiose 2HCl plays a fundamental role in the progression of targeted therapeutic drug delivery systems. Synonyms: Chitosan dimer; 4-O-(b-D-Glucosamine)-D-glucosamine; 2-Amino-4-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-D-glucose; 4-O-(2-Amino-2-deoxy-β-D-glucosyl)-D-glucosamine. CAS No. 577-76-4. Molecular formula: C12H24N2O9. Mole weight: 340.33. BOC Sciences 6
Chitobiose dihydrochloride Chitobiose Hydrochloride is an exceptional biomedical compound, exhibiting profound versatility in research of numerous ailments encompassing cancer and diabetes. Its indispensable role as a pivotal intermediate in chitin research and development imparts promising prospects to the realms of pharmaceutical conveyance platforms and tissue engineering. Synonyms: Chitobiose 2HCl; D-Glucose, 2-amino-4-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-, hydrochloride (1:2); 2-Amino-4-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-D-glucose hydrochloride (1:2); D-Glucose, 2-amino-4-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-, dihydrochloride; Chitobiose Hydrochloride; 4-O-(2-Amino-2-deoxy-β-D-glucosyl)-D-glucosamine dihydrochloride. Grade: ≥97% by HPLC. CAS No. 115350-24-8. Molecular formula: C12H24N2O9.2HCl. Mole weight: 413.25. BOC Sciences 6
Chitobiose GEL Chitobiose GEL. BOC Sciences 6
Chitobiose octaacetate Chitobiose octaacetate, a carbohydrate derivative, is a promising candidate for the treatment of osteoarthritis. Studies demonstrate that it inhibits cartilage-degrading enzymes, the primary culprits of joint degradation in the disease. Furthermore, it attenuates inflammation and pain associated with osteoarthritis. Experts are currently examining its potential as a therapeutic agent, while the manifold intricacies of its pharmacological workings prompt ongoing investigation. Synonyms: 2-acetamido-4-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-2-deoxy-alpha-D-glucose 1,3,3',4',6,6'-hexaacetate; 1-O,3-O,6-O-Triacetyl-4-O-[3-O,4-O,6-O-triacetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-(acetylamino)-2-deoxy-α-D-glucopyranose; N,N'-Diacetylchitobiose hexaacetate; α-D-Glucopyranose, 2-(acetylamino)-2-deoxy-4-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-, 1,3,6-triacetate; octaacetylchitobiose. Grade: ≥95%. CAS No. 7284-18-6. Molecular formula: C28H40N2O17. Mole weight: 676.62. BOC Sciences 6
chitobiosyldiphosphodolichol β-mannosyltransferase This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. Group: Enzymes. Synonyms: guanosine diphosphomannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose:chitobiosyldiphosphodolichol β-D-mannosyltransferase. Enzyme Commission Number: EC 2.4.1.142. CAS No. 83380-85-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2368; chitobiosyldiphosphodolichol β-mannosyltransferase; EC 2.4.1.142; 83380-85-2; guanosine diphosphomannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose:chitobiosyldiphosphodolichol β-D-mannosyltransferase. Cat No: EXWM-2368. Creative Enzymes
Chitodecaose Hydrochloride Chitodecaose Hydrochloride is an innovative and groundbreaking pharmaceutical compound derived from the polymer Chitodecaose, exhibiting a touch of uniqueness stemming from chitosan. Its multifaceted nature encompasses remarkable antiviral and antibacterial attributes that have garnered substantial attention. Synonyms: Chitodecaose 10HCl; D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, hydrochloride (1:10). Grade: ≥93% by HPLC. Molecular formula: C60H112N10O41.10HCl. Mole weight: 1994.17. BOC Sciences 6
Chitoheptaose Chitoheptaose, a versatile compound extensively employed in the biomedicine sector, exhibits tremendous promise for addressing diverse ailments, encompassing cancer and inflammatory disorders. Functioning as an immunomodulator, this product effectively regulates immune responses and fortifies the body's defense mechanisms. Synonyms: O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose. CAS No. 68232-35-9. Molecular formula: C42H79N7O29. Mole weight: 1146.11. BOC Sciences 6
Chitoheptaose heptahydrochloride Chitoheptaose heptahydrochloride is a chitosan oligosaccharide with antioxidant, anti-inflammatory, antiapoptotic and cardioprotective activities. Chitoheptaose heptahydrochloride significantly enhances the growth and photosynthesis parameters of wheat seedlings[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 127171-89-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7697D. MedChemExpress MCE
Chitoheptaose Hydrochloride Chitoheptaose Hydrochloride is a remarkable compound, unveiling unrivaled potential in personalized researchs by selectively modulating distinct molecular pathways. Its multifaceted utility spans across research of malignant neoplasms, inflammatory conditions and bacterial afflictions. Synonyms: Chitoheptaose 7HCl; Chitoheptaose heptahydrochloride; D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, heptahydrochloride; O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose heptahydrochloride. Grade: ≥96% by HPLC. CAS No. 127171-89-5. Molecular formula: C42H79N7O29.7HCl. Mole weight: 1401.33. BOC Sciences 6
Chitohexaose Chitohexaose, a chitosan oligosaccharide with anti-inflammatory effect, binds to the active site of TLR4 and inhibits LPS-induced inflammation. Synonyms: D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-; 2-Amino-2-deoxy-β-D-glucopyranosyl-(1->4)-2-amino-2-deoxy-β-D-glucopyranosyl-(1->4)-2-amino-2-deoxy-β-D-glucopyranosyl-(1->4)-2-amino-2-deoxy-β-D-glucopyranosyl-(1->4)-2-amino-2-deoxy-β-D-glucopyranosyl-(1->4)-2-amino-2-deoxy-D-glucose. Grade: ≥95%. CAS No. 41708-95-6. Molecular formula: C36H68N6O25. Mole weight: 984.95. BOC Sciences 6
Chitohexaose hexahydrochloride Chitohexaose hexahydrochloride, a chitosan oligosaccharide with anti-inflammatory effect, binds to the active site of TLR4 and inhibits LPS-induced inflammation. Synonyms: D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, hydrochloride (1:6); O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose hydrochloride (1:6). Grade: ≥95%. CAS No. 127171-88-4. Molecular formula: C36H74Cl6N6O25. Mole weight: 1203.72. BOC Sciences 6
Chitohexaose Hydrochloride Chitohexaose Hydrochloride is an extraordinary biomedical compound, an inherently-occurring oligosaccharide obtained from chitin. Profoundly endowed with anti-inflammatory and immunostimulating prowess, Chitohexaose Hydrochloride unveiling immense promise in the research of allergies, asthma and the augmentation of wound healing. Synonyms: Chitohexaose HCl; D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, hydrochloride (1:x); O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose hydrochloride. Grade: ≥96% by HPLC. CAS No. 133213-35-1. Molecular formula: C36H68N6O25.xHCl. Mole weight: 984.95 (free base). BOC Sciences 6
Chitolytic Chitosan - A-90101 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): (90.0 ≥ NMT 95.0). Viscosity (cps): <100. DDA%: High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - AL-120 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): (>80.0). Molecular Weight (kDa): <100. DDA%: Medium. MW: Medium-Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - AL-476 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): (>90.0). Molecular Weight (kDa): 80-400. Viscosity (cps): 30-400. DDA%: High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - AL-801 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): (>80.0). Molecular Weight (kDa): <400. DDA%: Medium. MW: Medium. ChitoLytic
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Chitolytic Chitosan - B-85-471692 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): (>85.0). Viscosity (cps): <100. DDA%: Medium. MW: Low. ChitoLytic
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Chitolytic Chitosan - B-95-545382 Chitolytic Chitosan. Source: Crustacean. Degree of Deacetylation (%): Deacetylation (95.6). Viscosity (cps): <100. DDA%: Very High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - C-M-85-401132 Chitolytic Chitosan. Source: Mushroom. Degree of Deacetylation (%): (90.0 ≥ NMT 95.0). Molecular Weight (kDa): 250 - 300. DDA%: High. MW: Medium. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - C-M-95-401132 Chitolytic Chitosan. Source: Mushroom. Degree of Deacetylation (%): (>95.0). Molecular Weight (kDa): 250 - 300. DDA%: Very High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan - C-M-98-501441 Chitolytic Chitosan. Source: Mushroom. Degree of Deacetylation (%): (≥98.0). Viscosity (cps): 600. DDA%: Very High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan Lactate - AL-10131 Chitolytic Chitosan Lactate. Source: Crustacean. Degree of Deacetylation (%): (≤95.0). Viscosity (cps): 33. DDA%: High. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan Oligosaccharide - CO-101211 Chitolytic Chitosan Oligosaccharide. Source: Crustacean. Degree of Deacetylation (%): (>85.0). Molecular Weight (kDa): <3. DDA%: Medium. MW: Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic Chitosan Oligosaccharide - MO-215241 Chitolytic Chitosan Oligosaccharide. Source: Mushroom. Degree of Deacetylation (%): (≥98.0). Molecular Weight (kDa): <3. DDA%: Very High. MW: Very Low. ChitoLytic
Canada, USA, Worldwide
Chitolytic N-Carboxymethyl Chitosan - CBM-1201 Chitolytic N-Carboxymethyl Chitosan. Source: Mushroom. Degree of Substitution: ≥90%. Viscosity (cps): (10 - 80). DDA%: High. MW: Low. ChitoLytic
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Chitolytic N,N,N-Trimethyl Chitosan - TMC-143 Chitolytic N,N,N-Trimethyl Chitosan. Source: Crustacean. Degree of Quaternization : >80%. ChitoLytic
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Chitolytic Woundcare Complex - CW-221 Chitolytic Woundcare Complex. Source: Crustacean. Categories: chitosan based products. ChitoLytic
Canada, USA, Worldwide
Chitononaose Hydrochloride Chitononaose Hydrochloride is a compound with remarkable antibacterial properties, rendering it an effective compound studying ailments like pneumonia and skin infections. Synonyms: Chitononaose 9HCl; O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→5)-2-amino-2-deoxy-D-glucose, hydrochloride (1:9). Grade: ≥93% by HPLC. Molecular formula: C54H101N9O37.9HCl. Mole weight: 1796.56. BOC Sciences 6
Chitooctaose 8HCl Chitooctaose 8HCl is an illustrious biomedical compound used to study the menacing clutches of cancer and diabetes. Synonyms: Chitosan octamer. CAS No. 127171-90-8. Molecular formula: C48H90N8O33.8HCl. Mole weight: 1598.95. BOC Sciences 6
Chitooctaose Hydrochloride Chitooctaose Hydrochloride is an exquisite and unparalleled biomedical compound, diligently dedicated to studying a myriad of perplexing bacterial infections and inflammatory maladies. Its venerated essence traverses the realms of antimicrobial and anti-inflammatory prowess, embracing the audacious battle against vexatious drug-resistant strains unyieldingly. Synonyms: Chitooctaose HCl; D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, hydrochloride (1:x). Grade: ≥95% by HPLC. CAS No. 133213-36-2. Molecular formula: C48H90N8O33.xHCl. Mole weight: 1307.26 (free base). BOC Sciences 6
Chitooctaose Hydrochloride Chitooctaose Hydrochloride is a chitin oligosaccharide created from the exoskeleton of crustaceans. Potential biomedical uses of chitin include gauze dressings displaying antibacterial activity, and as hemostatic agents. Also used in polymer coatings for automobiles as it remedies scratches via sunlight induced chemical bonding. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C48H90N8O33 8[HCl]. US Biological Life Sciences. USBiological 9
Worldwide
Chito-oligosaccharides hydrochloride Chito-oligosaccharides hydrochloride is an innovative biomedical compound boasting exceptional antimicrobial qualities, rendering it exceptionally efficacious in research of both bacterial and fungal infections. Consequently, Chito-oligosaccharides hydrochloride emerges as a formidable candidate for the research of gastritis, gastric ulcers and cutaneous maladies. Grade: ≥97% by HPLC. Molecular formula: (C6H13NO5·HCL)3-7. BOC Sciences 6
Chitopentaose Chitopentaose Hydrochloride (CPC) is an invaluable biomedical compound derived from chitosan unveiling an amalgamation of antimicrobial with antioxidant and immunomodulatory activities, excelling delivery systems and wound healing applications. It has aptitude to invigorate tissue regeneration and bolster osseous development. Synonyms: D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-; O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose; Chitopentose. Grade: ≥97% by HPLC. CAS No. 41708-94-5. Molecular formula: C30H57N5O21. Mole weight: 823.80. BOC Sciences 6
Chitopentaose pentahydrochloride Chitopentaose pentahydrochloride is a chitosan oligosaccharide with anti-inflammatory effect. Synonyms: Chitopentaose hydrochloride; D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-, hydrochloride (1:5); O-2-Amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-D-glucose hydrochloride (1:5); Chitopentose pentahydrochloride. CAS No. 117467-64-8. Molecular formula: C30H62Cl5N5O21. Mole weight: 1006.10. BOC Sciences 6
Chitosan Chitosan is a polysaccharide comprising copolymers of glucosamine and N-acetylglucosamine. CAS No. 9012-76-4. Product ID: PE-0188. Molecular formula: (C6H11NO4)n. Category: Binder Excipients; Thickener Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Capsule Excipients; Semi-Excipients for Solid Dosage Form; Suppository Bases; Thickener Excipients; Chitosan; PE-0188; (C6H11NO4)n; 9012-76-4; 9012-76-4. Appearance: White to off-white powder. Melting Point: 102.5°C. CD Formulation
Chitosan Chitosan is a deacetylated derivative of chitin. Chitosan is a polysaccharide present in the exoskeleton of a variety of crustaceans and cell walls of fungi. It can be used in the medical field and cosmetics manufacturing. In addition to its role in drug delivery, chitosan can also act as an adjuvant due to its immune-stimulating activity. Chitosan stimulates the immune system by activating the NLRP3 inflammasome, which produces potent IL-1b. When tested in an experimental model of vaccination, chitosan elicits a balanced Th1/Th2 response. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Deacetylated chitin; Poly(D-glucosamine); Poly-b-(1,4)-2-Amino-2-deoxy-D-glucose; 2-Amino-2-deoxy-(1,4)-b-D-glucopyranan; deacetylchitin; b-1,4-poly-D-glucosamine; poly-D-glucosamine; poly-(1,4-b-D-glucopyranosamine). CAS No. 9012-76-4. Molecular formula: [C7H15NO4]n. Mole weight: 60-120 kDa. BOC Sciences 6
Chitosan Chitosan deacetylation%: 90 - 95 , Viscosity (cps): 75. Chitosan (B-90-471692) Group: Chitosan. Grade: Medica Research, Food, Industrial. CAS Number: 9012-76-4. Pack Sizes: Grams: 100, 250, 1000+. Categories: Chitosan, Chitin, Chitosanase ChitoLytic
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Chitosan Chitosan. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. Neuchem
US and Canada
Chitosan Chitosan is a polysaccharide comprising copolymers of glucosamine and N-acetylglucosamine. CAS No. 9012-76-4. Product ID: PE-0238. Molecular formula: (C6H11NO4)n. Category: Film Former Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Film Former Excipients; Chitosan; PE-0238; (C6H11NO4)n; 9012-76-4; 9012-76-4. Appearance: White to off-white powder. Standard: PhEur; USP-NF. Melting Point: 102.5°C. CD Formulation
Chitosan Active ingredient chitosan is de-acylated chitin. Derived from crustacean shells. Used as film-former and hair-fixative. Also used as deodorising agent. It possesses antimicrobial and excellent skin care properties. It prevents the excessive generation of odor-forming substances. Alternative Names: Chitin, deacylated. CAS No. 9012-76-4. Purity: 95%. Product ID: ACM9012764-55. Molecular formula: C6H13NO4. Mole weight: 1526.5g/mol. IUPAC Name: Methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. Canonical SMILES: COC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)N)O[C@@H]3[C@H](O[C@H]([C@@H]([C@H]3O)N)O)CO)CO)CO)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O[C@H]9[C@@H]([C@H]([C@@H]([C@ Alfa Chemistry.
Chitosan Chitosan (B-95-545381) Deacetylation%: 95.6, Viscosity (cps): 66. Group: Chitosan. Grade: Medica Research, Food, Industrial. CAS Number: 9012-76-4. Pack Sizes: Grams: 100, 250, 1000+. Categories: Chitosan, Chitin, Chitosanase ChitoLytic
Canada, USA, Worldwide
Chitosan Active ingredient chitosan is de-acylated chitin. Derived from crustacean shells. Used as film-former and hair-fixative. Also used as deodorising agent. It possesses antimicrobial and excellent skin care properties. It prevents the excessive generation of odor-forming substances. Alternative Names: Chitin, deacylated. CAS No. 9012-76-4. Molecular formula: C6H13NO4. Mole weight: 1526.5g/mol. Purity: 95%. IUPAC Name: Methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. SMILES: COC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)N)O[C@@H]3[C@H](O[C@H]([C@@H]([C@H]3O)N)O)CO)CO)CO)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O[C@H]9[C@@H]([C@H]([C@@H]([C@H](O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O.… Alfa Chemistry Materials 2
Chitosan 100g Pack Size. Group: Carbohydrates, Sugars. Formula: (C6H11NO4)n. CAS No. 9012-76-4. Prepack ID 42000446-100g. Molecular Weight polymer. See USA prepack pricing. Molekula Americas
Chitosan Chitosan is a natural biopolymer produced by deacetylation of chitin, which is present in the exoskeleton of crustaceans (such as shrimp and crabs) as well as the cell wall of fungi. It is a linear polysaccharide with randomly distributed β-(1→4)-linked D-glucosamine and N-acetyl-D-glucosamine. It is biocompatible, biodegradable, and has properties such as being cationic in charge, film-forming, and antimicrobial. Applications: Attributable to its broad chemical properties, chitosan has found many industrial applications ranging from biomedicine to wastewater treatment processes. applications in medicine include the engineering of wound dressings that promote fast healing and prevent infection. it has also been used in drug delivery systems as a controlled-release carrier. in wastewater treatment processes, chitosan acts as a flocculant to remove heavy metals, dye colorants, and oils from industrial wastewater. it is also used commonly used as a food preservative and antimicrobial coating on perishables. Category: Dispersion excipients. CAS No. 9012-76-4. Product ID: PIE-0300. Molecular formula: C56H103N9O39. Mole weight: 1526.5. EINECS: 618-480-0. InChIKey: FLASNYPZGWUPSU-SICDJOISSA-N. Appearance: Yellow powder. Standard: USDMF. Protheragen
Chitosan Chitosan. CAS No. 9012-76-4. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. Cenik Chemicals
Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) Solid. CAS No. 9012-76-4. Molecular formula: C56H103N9O39. Mole weight: 1526.5g/mol. IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O. InChI: InChI=1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-… Alfa Chemistry Materials 6
Chitosan (20-100mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) Solid. CAS No. 9012-76-4. Molecular formula: C56H103N9O39. Mole weight: 1526.5g/mol. IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O. InChI: InChI=1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,… Alfa Chemistry Materials 6
Chitosan(20-100mPa.s, 0.5% in 0.5% Acetic Acid at 20deg C) Chitosan(20-100mPa.s, 0.5% in 0.5% Acetic Acid at 20deg C). Group: Molecular Biology. CAS No. 9012-76-4. Pack Sizes: 25g, 100g. US Biological Life Sciences. USBiological 9
Worldwide
Chitosan, 2-hydroxyethyl ether Chitosan, 2-hydroxyethyl ether. Synonyms: Aquacluster; Chitosan hydroxyethylate; Glycol chitosan; Hydroxyethyl chitosan. CAS No. 39280-86-9. BOC Sciences 6
Chitosan (5-20mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) Solid. CAS No. 9012-76-4. Molecular formula: C56H103N9O39. Mole weight: 1526.5g/mol. IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O. InChI: InChI=1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27… Alfa Chemistry Materials 6
Chitosan acetate Chitosan acetate. Synonyms: Chitosan, acetate (salt); Chitomost SK Acetic Acid; Chitopol A Green; Chitosan SK 10; Daichitosan 100DVL acetic acid salt; Daichitosan M; Kimica Chitosan A; Kitofuressyu L; Koyo Chitosan SK 10; Koyo Chitosan SK 400; Novafect 025; SK 10; SK 10 (polysaccharide); SK 400; SK 400 (polysaccharide); Vanson. CAS No. 87582-10-3. BOC Sciences 6
Chitosan acetate Chitosan acetate. CAS No: 9012-76-4 Sarchem Laboratories
Sarchem Laboratories New Jersey NJ
chitosanase A whole spectrum of chitosanases are now known (for more details, see http://rbrzezinski. recherche. usherbrooke. ca/). They can hydrolyse various types of links in chitosan. The only constant property is the endohydrolysis of GlcN-GlcN links, which is common to all known chitosanases. One known chitosanase is limited to this link recognition, while the majority can also recognize GlcN-GlcNAc links or GlcNAc-GlcN links but not both. They also do not recognize GlcNAc-GlcNAc links in partly acetylated chitosan. Group: Enzymes. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Chitosanase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3815; chitosanase; EC 3.2.1.132; 51570-20-8. Cat No: EXWM-3815. Creative Enzymes
Chitosanase Chitosanase is a glycosyl hydrolase that catalyzes the endo hydrolysis of β-1,4-glycosidic bonds of partially acetylated chitosan to release chitosan oligosaccharides (COS). Chitosanases can convert high molecular weight chitosan into functional chitooligosaccharides with low molecular weight[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 51570-20-8. Pack Sizes: 10 U. Product ID: HY-P2859. MedChemExpress MCE
Chitosanase 46A from Bacillus subtilis, Recombinant Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 29.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 46A. Cat No: NATE-1376. Creative Enzymes
Chitosanase 8B from Bacillus cereus, Recombinant Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 47.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 8B. Cat No: NATE-1375. Creative Enzymes
Chitosanase from Bacillus sp. (food grade) Chitosanase is a powdered chitosanase preparation made by submerged fermentation of a selected strain of the bacterium Bacillus sp. The enzyme catalyzes the breakdown of chitosan, a partially or completely de-acetylated derivative of chitin (β-1,4 homopolymer of N-acetyl glucosamine). Applications: Chitosanase can be used for hydrolyzing chitosan (degree of de-acetylatin: 40~100%). especially, it can be used for the production of chitosan oligosaccharides from chitosan, which have a variety of biological activities such as immuno-stimulating activity, anti-tumor activity, anti-microbial activity, etc. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Chitosanase. Mole weight: 45,000Da estimated by SDS-PAGE. Activity: 35,000U/g. Storage: The product should be stored in a cool, dry environment with temperatures below 4°C. Form: White or light yellow colored, freeze-dried powder. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Cat No: CHIC-001. Creative Enzymes
Chitosan (B-85-471692) Deacetylation%: 85 - 90 , Viscosity (cps): 70. Chitosan (B-85-471692) Group: Chitosan. Grade: Medica Research, Food, Industrial. CAS Number: 9012-76-4. Pack Sizes: Grams: 100, 250, 1000+. Categories: Chitosan, Chitin, Chitosanase ChitoLytic
Canada, USA, Worldwide
Chitosan Dry Flake (D-DF-85-751449) Deacetylation%: 86.5 , Molecular Weight (kDa): 250 - 300 , Viscosity (cps): 1200. Chitosan Dry Flake (D-DF-85-751449) Group: Chitosan. Grade: Medica Research, Food, Industrial. CAS Number: 9012-76-4. Pack Sizes: Grams: 100, 250, 1000+. Categories: Chitosan, Chitin, Chitosanase ChitoLytic
Canada, USA, Worldwide
Chitosan, food grade 100g Pack Size. Group: Aroma Chemicals, Biochemicals, Building Blocks, Carbohydrates, Organics. Formula: (C6H11NO4)n. CAS No. 9012-76-4. Prepack ID 90024357-100g. Molecular Weight polymer. See USA prepack pricing. Molekula Americas
Chitosan from shrimp shells Solid. CAS No. 9012-76-4. Molecular formula: C56H103N9O39. Mole weight: 1526.5g/mol. IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate. SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O. InChI: InChI=1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,3… Alfa Chemistry Materials 3
Chitosan (≥90% deacetylated, Low viscosity,<200mPa.s) Chitosan (Deacetylated chitin) (≥90% deacetylated, Low viscosity,<200mPa.s) is a polysaccharide obtained by deacetylating chitin, and exhibits antimicrobial activity against various bacteria and fungi[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Deacetylated chitin (≥90% deacetylated, Low viscosity,<200mPa.s); Poly(D-glucosamine) (≥90% deacetylated, Low viscosity,<200mPa.s). CAS No. 9012-76-4. Pack Sizes: 10 g; 25 g. Product ID: HY-B2144E. MedChemExpress MCE
Chitosan (≥95% deacetylated,viscosity 100-200 mPa.s) Chitosan (Deacetylated chitin) (≥95% deacetylated,viscosity 100-200 mPa.s) is a polysaccharide obtained by deacetylating chitin, and exhibits antimicrobial activity against various bacteria and fungi[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Deacetylated chitin (≥95% deacetylated,viscosity 100-200 mPa.s); Poly(D-glucosamine) (≥95% deacetylated,viscosity 100-200 mPa.s). CAS No. 9012-76-4. Pack Sizes: 25 g. Product ID: HY-B2144C. MedChemExpress MCE
Chitosanglutamate Chitosanglutamate is an innovative biomedical compound for efficacious drug delivery, merging the forces of chitosan and glutamic acid. It exhibits auspicious outcomes for studying maladies encompassing cancer, diabetes and cardiovascular anomalies. Synonyms: Chitosan glutamate; L-Glutamic acid, compd. with chitosan; Chitosan, L-glutamate (salt); Chitosan glutamic acid salt; Chitosan Seacure G 210; Pronova B-MV; Protasan. G; Protasan G 113; Protasan G210; Prota. CAS No. 84563-76-8. BOC Sciences 6
Chitosan hydrochloride Chitosan hydrochloride is the chloride salt of an unbranched binary heteropolysaccharide consisting of the two units N-acetyl-D-glucosamine and D-glucosamine. Synonyms: Poliglusam hydrochloride; Chitosan chloride; L 0221-20FD; Protasan CL 110; Protasan CL 113; Protasan Cl 210; Protasan CL 213; Protasan CL 214; Protasan UP CL 214; Protasan UP-CL 113; Protasan UP-CL 210; Protasan UP-CL 213; SC 12181; Sea Cure 113; Sea Cure 311; Sea Cure CL 110; Sea Cure CL 113; Sea Cure CL 210; Sea Cure CL 214; Sea Cure CL 310; Sea Cure CL 313. CAS No. 70694-72-3. BOC Sciences 6

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