Chitosan - medium viscosity, 200-400 mPa.s , CAS No.9012-76-4

CAS: 9012-76-4 Cat. No.: C105802 Formule: (C₆H₁₁NO₄)n Numéro CE: 618-480-0

GRADE & PURITY medium viscosity, 200-400 mPa.s

Synonyms

Kytex M | Toluene, o-chloro- | Chitopearl BCW 3505 | Chitopearl BCW 2500 | YEA | Toluene, o-bromo- | AKOS037652919 | Chitopearl BCW 3507 | Chitosan | Sea Cure F | Q408510 | AKOS015918343 | N-[(2S,3R,4R,5S,6R)-5-[[(2S,3R,4R,5S,6R)-3-amino-5-[[(2S,3R,4R,5S,

Storage

Store at 2-8°C

Shipped In

Wet ice

Vue d’ensemble

Flocculant, protein precipitation, encapsulating agent and aqueous thickener. Forms gels with multivalent anions. Gives clear solutions that dry to strong, clear films.

Specifications

Synonymes

Kytex M | Toluene, o-chloro- | Chitopearl BCW 3505 | Chitopearl BCW 2500 | YEA | Toluene, o-bromo- | AKOS037652919 | Chitopearl BCW 3507 | Chitosan | Sea Cure F | Q408510 | AKOS015918343 | N-[(2S,3R,4R,5S,6R)-5-[[(2S,3R,4R,5S,6R)-3-amino-5-[[(2S,3R,4R,5S,

Spécifications et pureté

medium viscosity, 200-400 mPa.s

Conditions de stockage de stockage

Store at 2-8°C

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Noms et identifiants

• Pubchem Sid: 508813172
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508813172
• 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
• InChIKey: FLASNYPZGWUPSU-SICDJOISSA-N
• 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-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48+,49+,50+,51+,52+,53+,54+,55+/m1/s1
• Isomères 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

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Oligosaccharides
• Alternative Parents: Aminoglycosides O-glycosyl compounds Oxanes Methylcarbamates 1,2-aminoalcohols Secondary alcohols Hemiacetals Organic carbonic acids and derivatives Acetals Oxacyclic compounds Monoalkylamines Primary alcohols Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oligosaccharide - Aminoglycoside core - Glycosyl compound - O-glycosyl compound - Amino saccharide - Oxane - Methylcarbamate - Carbamic acid ester - 1,2-aminoalcohol - Secondary alcohol - Hemiacetal - Carbonic acid derivative - Acetal - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Primary alcohol - Primary aliphatic amine - Primary amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Alcohol - Organopnictogen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Solubilité: Soluble in acetic acid, adipic acid, formic acid, lactic acid, propionic acid and succinic acid.Insoluble in phosphoric acid, sulfuric acid, neutral and alkaline media.
• Point de fusion (°C): 102.5°C
• Poids moléculaire: 1526.500 g/mol
• XLogP3: -21.400
• Hydrogen Bond Donor Count: 29
• Hydrogen Bond Acceptor Count: 47
• Rotatable Bond Count: 27
• Exact Mass: 1525.64 Da
• Monoisotopic Mass: 1525.64 Da
• Topological Polar Surface Area: 808.000 Ų
• Heavy Atom Count: 104
• Formal Charge: 0
• Complexity: 2630.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 45
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1