Chitosan - high viscosity, ＞400 mPa.s,from shrimp shells , CAS No.9012-76-4

CAS: 9012-76-4 Cat. No.: C105803 분자식: (C₆H₁₁NO₄)n EC 번호: 618-480-0

GRADE & PURITY high viscosity, ＞400 mPa.s,from shrimp shells

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

개요

Chitosan is a naturally occurring product which may be used as a biocompatible, antibacterial, and environmentally friendly polyelectrolyte biomaterial. The applications of chitosan include uses in water treatment, chromatography, textile treatment for antimicrobial activity, novel fibers for textiles, biomedical devices, and microcapsule implants for controlled release in drug delivery, among others. The degree of acetylation of chitosan may be determined via titration methods or dye binding.
A naturally occurring biocompatible, antibacterial polyelectrolyte biomaterial

Specifications

동의어

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,

사양 및 순도

high viscosity, ＞400 mPa.s,from shrimp shells

보관 조건

Store at 2-8°C

배송

Wet ice

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이름과 식별자

Pubchem Sid

508813169

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813169

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

이성체 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
    • 분류 Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• 분류: 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
• 설명: 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

화학 및 물리적 특성

• 용해성: Soluble in 1M acetic acid (10 mg/ml).
• 감도: Heat & Light & Moisture sensitive
• 녹는점(°C): 102.5°C
• 분자량: 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