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| Product | Description | |
|---|---|---|
| Chitin Nanoparticles | Chitin Nanoparticles. Group: Clay nanopowders. CAS No. 1398-61-4. Molecular formula: 770.8g/mol. Mole weight: C30H50N4O19. >99%. |  |
| Chitin Oligosaccharides | Chitin Oligosaccharides. CAS No. 1398-61-4. Product ID: 4-00647. |  |
| Chitinovorin A | Chitinovorin A is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Molecular formula: C26H41N9O11S. Mole weight: 687.73. |  |
| 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*)))-. Grades: >98%. CAS No. 95722-76-2. Molecular formula: C29H46N10O12S. Mole weight: 758.80. | |
| 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. | |
| Chitin phosphate | Chitin phosphate. Product ID: 5-02283. Purity: highly phosphorylated chitin (P 5-7%). Properties: water insoluble. | |
| Chitin phosphate sulphate | phosphorylated and sulfated chitin. Product ID: 5-02284. Properties: Water soluble, salt free sulfated with potential biological activity. | |
| Chitin sulphate | Chitin sulphate. Product ID: 5-02537. Properties: Water soluble, salt free anionic polysaccharide with potential biological activity. | |
| 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. |  |
| Chitobiose 2HCl | Chitobiose 2HCl 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 dihydrochloride; 4-O-(b-D-Glucosamine)-D-glucosamine. CAS No. 577-76-4. Molecular formula: C12H24N2O9 2HCl. Mole weight: 413.25. | |
| Chitobiose dihydrochloride | Chitobiose dihydrochloride, a chitosan oligosaccharide, is a dimer of β-1,4-linked glucosamine units [1]. Uses: Scientific research. Group: Natural products. CAS No. 115350-24-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7697B. |  |
| Chitobiose dihydrochloride | Chitobiose dihydrochloride. CAS No. 577-76-4. Product ID: 5-02409. Molecular formula: GlcNb1-4GlcNb. Mole weight: 413.25. Purity: >98% (HPLC). | |
| Chitobiose GEL | | |
| Chitobiose Hydrochloride | 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. Grades: ≥97% by HPLC. Molecular formula: C12H24N2O9·2HCL. Mole weight: 413.25. | |
| Chitobiose octaacetate | Chitobiose octaacetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N'-Diacetylchitobiose hexaacetate. Product Category: Heterocyclic Organic Compound. Appearance: White Crystalline Solid. CAS No. 41670-99-9. Molecular formula: C28H40N2O17. Mole weight: 676.6. Purity: 96%+. IUPACName: [(2R,3S,4R,5R)-5-Acetamido-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4,6-diacetyloxyoxan-2-yl]methyl acetate. Canonical SMILES: CC(=O)NC1C(C(C(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C. Product ID: ACM41670999. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 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. Grades: ≥95%. CAS No. 7284-18-6. Molecular formula: C28H40N2O17. Mole weight: 676.62. | |
| 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. | |
| Chitodecaose 10HCl | Chitodecaose 10HCl is an exceptional biomedical agent, widely employed as an efficacious measure for targeting and impeding the activity of pivotal enzymes implicated in the intricate pathogenesis of ailments like cancer and neurodegenerative maladies. Synonyms: Chitodecaose Hydrochloride; Chitosan Decamer. Molecular formula: C60H112N10O41 10HCl. Mole weight: 1994.18. | |
| 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. Grades: ≥93% by HPLC. Molecular formula: C60H112N10O41·10HCL. Mole weight: 1994.17. | |
| Chitoheptaose 7HCl | Chitoheptaose 7HCl, 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: Chitoheptaose 7-hydrochloride; 68232-35-9. CAS No. 68232-35-9. Molecular formula: C42H79N7O29 7HCl. Mole weight: 1401.34. | |
| Chitoheptaose heptahydrochloride | Chitoheptaose heptahydrochloride. CAS No. 68232-35-9. Product ID: 5-02443. Molecular formula: (GlcNb1-4)7. Mole weight: 1,401.34. Purity: >98% (HPLC). Properties: liquid. | |
| 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. Grades: ≥96% by HPLC. Molecular formula: C42H79N7O29·7HCL. Mole weight: 1401.33. | |
| Chitohexaose 6HCl | Cas No. 41708-95-6. | |
| Chitohexaose hexahydrochloride | Chitohexaose hexahydrochloride. CAS No. 41708-95-6. Product ID: 5-02410. Molecular formula: (GlcNb1-4GlcNb)3. Mole weight: 1,203.73. Purity: >98% (HPLC). Reference: J. Microbiol. Biotechnol., 4, 343-348, 1994; Am. J. Clin. Nutr., 67, 445-51, 1998. | |
| 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 6HCl. Grades: ≥96% by HPLC. Molecular formula: C36H68N6O25·6HCL. Mole weight: 1203.72. | |
| 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. Grades: ≥93% by HPLC. Molecular formula: C54H101N9O37·9HCL. Mole weight: 1796.56. | |
| 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. | |
| 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. |  Worldwide |
| 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 8HCl. Grades: ≥95% by HPLC. Molecular formula: C48H90N8O33·8HCL. Mole weight: 1598.94. | |
| 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. Grades: ≥97% by HPLC. Molecular formula: (C6H13NO5·HCL)3-7. | |
| Chitopentaose 5HCl | Chitopentaose 5HCl is an indispensable biomolecular compound functioning as a fundamental constituent in pharmacoresearchs targeting microbial infestations and inflammatory pathologies. Synonyms: Chitopentaose pentahydrochloride; Chitosan Pentamer extrapure. CAS No. 35061-50-7. Molecular formula: C30H57N5O21.5HCl. Mole weight: 1006.01. | |
| Chitopentaose Hydrochloride | 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: Chitopentaose 5HCl. Grades: ≥97% by HPLC. Molecular formula: C30H57N5O21·5HCL. Mole weight: 1006.1. | |
| 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 |  Canada, USA, Worldwide |
| 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. |  |
| 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 | Canada, USA, Worldwide |
| Chitosan | Chitosan. Grades: high purity. CAS No. 9012-76-4. Product ID: 4-00560. | |
| 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. |  California |
| 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). Grades: DAC degree?90%+. CAS No. 9012-76-4. Molecular formula: [C7H15NO4]n. Mole weight: 60-120 kDa. | |
| 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. Uses: In the agricultural sector: as growth promoters, bio-pesticides, feed additives, seed treatment. Group: 3d printing materials biodegradable polymerspolysaccharide. Alternative Names: Chitin, deacylated. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C6H13NO4. 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 | |
| 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. |  |
| 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. | |
| 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. Uses: In the agricultural sector: as growth promoters, bio-pesticides, feed additives, seed treatment. Group: other nano materials. Alternative Names: Chitin, deacylated. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C6H13NO4. 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 | |
| Chitosan | Polyglucosamine. also available in pharma grade. Grades: high purity powder, ash <1.0%, degree of deacetylation>80%. CAS No. 9012-76-4. Product ID: 4-00022. Properties: mp >278°C. Source : | |
| Chitosan | Chitosan. Grades: high purity powder. CAS No. 9012-76-4. Product ID: 4-00551. Properties: degree of deacetylation 80%. Source : from crab shells. | |
| Chitosan | Chitosan. Grades: high purity powder. CAS No. 9012-76-4. Product ID: 4-00552. Properties: degree of deacetylation 90%. Source : from crab shells. Reference: Cancer, 55, 2498, 1985; Carbohydr. Res., 47, 90, 1976; Biopolymers, 33, 561, 1983. | |
| Chitosan | Chitosan. Grades: high purity powder. CAS No. 9012-76-4. Product ID: 4-00553. Properties: degree of deacetylation 100%. | |
| Chitosan | Chitosan. Grades: high purity powder. CAS No. 9012-76-4. Product ID: 4-00554. Properties: antitumor agent. Source : from Lentinan edodes. MFCD No. MFCD01773536. | |
| Chitosan | Chitosan. Grades: high purity. CAS No. 9012-76-4. Product ID: 4-00559. Properties: granule size <0.2 mm, ash <1.0%, degree of deacetylation>80%. Source : from crab shells. | |
| Chitosan | Chitosan. CAS No. 9012-76-4. Product ID: 4-00576. Purity: degree of deacetylation >80%. Properties: moisture <12%, gel strength 700 g/cm2, pH 7-9. | |
| Chitosan | Chitosan. Grades: biomedical grade. CAS No. 9012-76-4. Product ID: 8-01024. | |
| Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) | Solid. Group: Polymers. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C56H103N9O39. 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=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, 1 | |
| Chitosan(200-600mPa.s, 0.5% in 0.5% Acetic Acid at 20deg C) | Chitosan(200-600mPa.s, 0.5% in 0.5% Acetic Acid at 20deg C). Group: Molecular Biology. CAS No. 9012-76-4. Pack Sizes: 25g, 500g. US Biological Life Sciences. | Worldwide |
| Chitosan (20-100mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) | Solid. Group: Polymers. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C56H103N9O39. 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=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, 1H | |
| 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. | Worldwide |
| Chitosan (5-20mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) | Solid. Group: Polymers. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C56H103N9O39. 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=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, | |
| Chitosan(5-20mPa.s, 0.5% in 0.5% Acetic Acid at 20deg C) | Chitosan(5-20mPa.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. | Worldwide |
| Chitosan acetate | Chitosan acetate. CAS No: 9012-76-4 |  Sarchem Laboratories New Jersey NJ |
| Chitosan Ascorbate | Chitosan Ascorbate. Product ID: 4-00641. | |
| 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. | |
| CHITOSANASE | Synonyms: CHITOSANASE; CHITOSANASE, STREPTOMYCES SPECIES N174; CHITOSAN N-ACETYLGLUCOSAMINOHYDROASE; CHITOSAN N-ACETYLGLUCOSAMINOHYDROLASE; EC 3.2.1.132; chitosanase from streptomyces sp. N174; Chitosanase, Streptomyces sp.N174; CHITOSANASE FROM STREPTOMYCES SP. N174, RE. Grades: 95%. CAS No. 51570-20-8. | |
| 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. | |
| 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. | |
| 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. | |
| Chitosan-Azure | Chitosan-Azure. Product ID: 9-01392. | |
| Chitosan-Azure | . Product ID: 9-01083. | |
| 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 | 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 | Canada, USA, Worldwide |
| Chitosan Evening Primrose Oil Complex | Chitosan Evening Primrose Oil Complex. Product ID: 4-00645. Reference: Biochim. Biophys. Acta, 293, 197-202, 1973. | |
| 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. | |
| Chitosan from shrimp shells | Solid. Group: Polysaccharide. CAS No. 9012-76-4. Product ID: 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. Molecular formula: 1526.5g/mol. Mole weight: C56H103N9O39. 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=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 | |
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