Maltose solution - BioReagent, Suitable for molecular biology, ~20% in H2O , CAS No.69-79-4

CAS: 69-79-4 Cat. No.: M120965 Formula: C₁₂H₂₂O₁₁ Molecular Weight: 342.3 Beilstein Registry Number: 93798 EC Number: 200-716-5

GRADE & PURITY BioReagent, Suitable for molecular biology, ~20% in H2O

Synonyms

Maltose (8CI)|Maltose anhydrous|Maltose, pure|beta-D-Cellobiose|SUNMALT-S|Glcalpha1-4Glcbeta|B-D-GLUCOPYRANOSE, 4-O-A-D-GLUCOPYRANOSYL-|Maltobiose|4-(alpha-D-Glucosido)-D-glucose|maltose|D-Glucose, 4-O-alpha-D-glucopyranosyl-|D-Glucose, 4-O-alpha-D-glucopyranosyl- (6CI,9CI)|beta-maltose|beta-D-Maltose|Finetose|.BETA.-D-MALTOSE|.BETA.-D-CELLOBIOSE|MALTOSE .BETA.-ANOMER|4-(alpha-D-Glucopyranosido)-alpha-glucopyranose|beta-D-glucopyranose, 4-O-alpha-D-glucopyranosyl-|(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol|Maltose HH|D-(+)-Maltose|Maltroise|4-O-alpha-D-Glucopyranosyl-D-glucose|Glca1-4Glcb|alpha-D-Glcp-(1->4)-beta-D-Glcp|Sunmalt|Finetose F|Pharmakon1600-01301024|Sunmalt S|.beta.-D-Glucopyranose, 4-O-.alpha.-D-glucopyranosyl-|BETA-D-GLUCOPYRANOSYL(1-4)-D-GLUCOPYRANOSE|D-Maltose|4-O-alpha-D-glucopyranosyl-beta-D-glucopyranose|INSULIN, (ARG-INSULIN)|.BETA.-MALTOSE|Maltose HHH|Malt sugar|cellobiose|Advantose 100|alpha-D-glucopyranose-(1->4)-beta-D-glucopyranose|Maltodiose|(2R,3R,4R,5S,6R)-6-(Hydroxymethyl)-5-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2,3,4-triol|(2R,3R,4R,5R)-2,3,5,6-Tetrahydroxy-4-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal|(2R,3S,4S,5R,6R)-2-methylol-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-methylol-tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol|alpha-D-glucopyranosyl-(1->4)-beta-D-glucopyranose|Maltose beta-anomer

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

Maltose (8CI) | Maltose anhydrous | Maltose, pure | beta-D-Cellobiose | SUNMALT-S | Glcalpha1-4Glcbeta | B-D-GLUCOPYRANOSE, 4-O-A-D-GLUCOPYRANOSYL- | Maltobiose | 4-(alpha-D-Glucosido)-D-glucose | maltose | D-Glucose, 4-O-alpha-D-glucopyranosyl- | D-Glucose, 4-O-alpha-D-glucopyranosyl- (6CI,9CI) | beta-maltose | beta-D-Maltose | Finetose Show more

Specifications & Purity

BioReagent, Suitable for molecular biology, ~20% in H2O

Storage

Argon charged,Room temperature

Shipped In

Normal

Grade

BioReagent, Suitable for molecular biology

Names and Identifiers

Pubchem Sid

488180030

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180030

Canonical Smiles

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

IUPAC Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol

InChIKey

GUBGYTABKSRVRQ-QUYVBRFLSA-N

INCHI

1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5-,6+,7-,8-,9-,10-,11-,12-/m1/s1

Isomeric SMILES

C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)O)CO)O)O)O)O

WGK Germany

2

Alternate CAS

6363-53-7

Molecular Weight

342.3

Beilstein

93798

Reaxy-Rn

1351180

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1351180&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Disaccharides Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: O-glycosyl compound - Disaccharide - Oxane - Secondary alcohol - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - 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: maltose

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

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in acetone, hot benzene, concentrated sulfuric acid, hot dilute alkali and most organic solvents.
• Sensitivity: Moisture sensitive
• Molecular Weight: 342.300 g/mol
• XLogP3: -4.700
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 4
• Exact Mass: 342.116 Da
• Monoisotopic Mass: 342.116 Da
• Topological Polar Surface Area: 190.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 382.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 10
• 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