Methylcellulose（MC） - 3500-5600mPa · s, 2% aqueous solution at 20 ℃ , CAS No.9004-67-5

CAS: 9004-67-5 Cat. No.: M742525 Numéro CE: 618-391-7 PubChem CID: 51063134

QUALITÉ & PURETÉ 3500-5600mPa · s, 2% aqueous solution at 20 ℃

Storage

Room temperature,Argon charged

Shipped In

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Vue d’ensemble

Methyl cellulose is a water-soluble, non-ionic polymer with hydrophilic glucosidic bonds, derived from the polysaccharide cellulose. 

Purpose

Methyl cellulose has been used:
in colony forming assays 
for sperm motility assessment 
for the generation of spheroids 
in preparation of agar beads 

Spécifications

Spécifications et pureté

3500-5600mPa · s, 2% aqueous solution at 20 ℃

Mécanismes biochimiques et physiologiques

Methyl cellulose mediates stabilization of oil, water and air mixtures, like foam, by emulsification. Methyl cellulose is used as a binder and thickener for various adhesives.[1][2] It is also used as a treatment of constipation.

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

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Noms et identifiants

Pubchem Sid

528773496

Sourires canoniques

[*]OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO[*])O[C@@H](O[*])[C@H](O[*])[C@H]2O[*])[C@H](O[*])[C@@H](O[*])[C@@H]1O[*]

IUPAC Name

(5R)-2,3,4-trimethoxy-6-(methoxymethyl)-5-[(2S)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane

InChIKey

YLGXILFCIXHCMC-JHGZEJCSSA-N

INCHI

1S/C20H38O11/c1-21-9-11-13(23-3)15(24-4)18(27-7)20(30-11)31-14-12(10-22-2)29-19(28-8)17(26-6)16(14)25-5/h11-20H,9-10H2,1-8H3/t11?,12?,13?,14-,15?,16?,17?,18?,19?,20+/m1/s1

Isomères SMILES

COCC1[C@H](C(C(C(O1)OC)OC)OC)O[C@H]2C(C(C(C(O2)COC)OC)OC)OC

WGK Allemagne

1

RTECS

FJ5959000

PubChem CID

51063134

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 O-glycosyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Disaccharides Oxanes Oxacyclic compounds Dialkyl ethers Acetals Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: O-glycosyl compound - Disaccharide - Oxane - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Acetal - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
• 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

• Sensibilité: Moisture sensitive
• Poids moléculaire: 454.500 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 12
• Exact Mass: 454.241 Da
• Monoisotopic Mass: 454.241 Da
• Topological Polar Surface Area: 102.000 Ų
• Heavy Atom Count: 31
• Formal Charge: 0
• Complexity: 496.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 8
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1