Polysucrose 400 - pulver, durchschnittliche Mw 400K , CAS No.26873-85-8

CAS: 26873-85-8 Cat. No.: P122394 EG-Nummer: 608-012-3 PubChem CID: 88330506

GRADE & PURITY powder,average Mw 400K

Synonyms

A-D-Glucopyranoside, | A852961 | Sucrose-epichlorohydrin copolymer | 2-(chloromethyl)oxirane;(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol | SCHEMBL8603704 | A-D-fructofuranosyl,

Storage

Room temperature

Shipped In

Normal

Übersicht

Polysucrose ist wasserlöslich, ungiftig, resistent gegen Darmenzyme, kugelförmig und kann mit einer Molekulargewichtsverteilung hergestellt werden, die der Größe vieler normaler Nahrungsproteine entspricht.
Sie wird für die Zellseparation und die Isolierung von Organellen verwendet. Polysucrose wurde in einer Studie zur Entwicklung einer neuen Methode für die Reinigung menschlicher beweglicher Spermien verwendet. Sie wurde auch in einer Studie verwendet, in der die antiproliferativen und antitumoralen Aktivitäten von D-reversen Peptiden untersucht wurden.

Specifications

Synonyme

A-D-Glucopyranoside, | A852961 | Sucrose-epichlorohydrin copolymer | 2-(chloromethyl)oxirane;(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol | SCHEMBL8603704 | A-D-fructofuranosyl,

Spezifikationen & Reinheit

pulver, durchschnittliche Mw 400K

Biochemische und physiologische Mechanismen

Synthetic high molecular weight polymer made by the copolymerization of sucrose and epichlorohydrin. The molecules have a branched structure with a high content of hydroxyl groups giving a good solubility in aqueous solutions.

Storage

Room temperature

Verschickt in

Normal

Hinweis

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Namen und Kennungen

Pubchem Sid

508816219

Kanonisches Lächeln

C1C(O1)CCl.C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O

IUPAC Name

2-(chloromethyl)oxirane;(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

InChIKey

IACFXVUNKCXYJM-AKSHDPDZSA-N

INCHI

1S/C12H22O11.C3H5ClO/c13-1-4-6(16)8(18)9(19)11(21-4)23-12(3-15)10(20)7(17)5(2-14)22-12;4-1-3-2-5-3/h4-11,13-20H,1-3H2;3H,1-2H2/t4-,5-,6-,7-,8+,9-,10+,11-,12+;/m1./s1

Isomere SMILES

C1C(O1)CCl.C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)CO)O)O)CO)O)O)O)O

WGK Deutschland

3

PubChem CID

88330506

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Ebene5 Glycosyl compounds
          • Ebene6 O-glycosyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Disaccharides C-glycosyl compounds Ketals Oxanes Oxolanes Secondary alcohols Polyols Oxacyclic compounds Epoxides Dialkyl ethers Primary alcohols Organochlorides Hydrocarbon derivatives Alkyl chlorides
• Molecular Framework: Not available
• Substituents: C-glycosyl compound - Disaccharide - O-glycosyl compound - Ketal - Oxane - Oxolane - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Dialkyl ether - Ether - Oxirane - Hydrocarbon derivative - Organohalogen compound - Organochloride - Primary alcohol - Alkyl halide - Alkyl chloride - Alcohol - Aliphatic heteromonocyclic compound
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Hygroscopic
• Spezifische Drehung [α]: [α]20/D 56.5°, c = 1% (w/v) in water
• Molekulargewicht: 434.820 g/mol
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 6
• Exact Mass: 434.119 Da
• Monoisotopic Mass: 434.119 Da
• Topological Polar Surface Area: 202.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 433.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 9
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3