D-(+)-Maltose monohydrate - analytical standard , CAS No.6363-53-7

CAS: 6363-53-7 Cat. No.: M104817 Fórmula: C₁₂H₂₂O₁₁•H₂O Peso molecular: 360.31 Beilstein Registry Number: 93798 Número CE: 613-294-6 PubChem CID: 23615261

GRAU & PUREZA Analytical standard

Synonyms

D-(+)-Maltose monohydrate, from potato, >=99% | Maltose monohydrate | Maltose Monohydrate, Pharmaceutical Secondary Standard; Certified Reference Material | AC-34514 | D-(+)-Maltose monohydrate, puriss. | D-(+)-Maltose monohydrate, Vetec(TM) reagent grade

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Visão geral

Usually used as a substrate for the identification, differentiation and characterization of enzymes, and also used to study maltose-binding proteins and disaccharide transport systems.

Especificações

Sinónimos

D-(+)-Maltose monohydrate, from potato, >=99% | Maltose monohydrate | Maltose Monohydrate, Pharmaceutical Secondary Standard; Certified Reference Material | AC-34514 | D-(+)-Maltose monohydrate, puriss. | D-(+)-Maltose monohydrate, Vetec(TM) reagent grade

Especificações e pureza

analytical standard

Mecanismos bioquímicos e fisiológicos

Maltose contains two glucose molecules with an α(1→4) glycosidic linkage.Tt exists in many food products, including beer, cereals, and pasta, can be derived from starch in food through the action of amylase.

Condições de armazenamento de armazenamento

Room temperature,Argon charged,Desiccated

Enviado em

Normal

Grau

Padrão analítico

Nomes e identificadores

Pubchem Sid

528763991

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528763991

Sorrisos canónicos

C(C1C(C(C(C(O1)OC(C(CO)O)C(C(C=O)O)O)O)O)O)O.O

IUPAC Name

(2R,3R,4R,5R)-2,3,5,6-tetrahydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal;hydrate

InChIKey

HBDJFVFTHLOSDW-DNDLZOGFSA-N

INCHI

1S/C12H22O11.H2O/c13-1-4(16)7(18)11(5(17)2-14)23-12-10(21)9(20)8(19)6(3-15)22-12;/h1,4-12,14-21H,2-3H2;1H2/t4-,5+,6+,7+,8+,9-,10+,11+,12+;/m0./s1

SMILES isoméricas

C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)O)O)O)O.O

WGK Alemanha

3

RTECS

OO5250000

PubChem CID

23615261

Peso molecular

360.31

Beilstein

93798

Reaxy-Rn

5784659

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty acyl glycosides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty acyl glycosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acyl glycosides of mono- and disaccharides
• Alternative Parents: Alkyl glycosides O-glycosyl compounds Disaccharides Oxanes Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Beta-hydroxy aldehyde - Oxane - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aldehyde - Alcohol - Primary alcohol - Aliphatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
• 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

Propriedades químicas e físicas

• Solubilidade: Soluble in water.
• Sensibilidade: Hygroscopic.
• Rotação específica [α]: 130° (C=10,H2O(add NH4aq.(2+3)))
• Ponto de fusão (°C): 130°C
• Peso molecular: 360.310 g/mol
• Hydrogen Bond Donor Count: 9
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 8
• Exact Mass: 360.127 Da
• Monoisotopic Mass: 360.127 Da
• Topological Polar Surface Area: 198.000 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 367.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 9
• 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: 2

XLogP3