Galactinol Hydrate - ≥99%(HPLC) , CAS No.3687-64-7

CAS: 3687-64-7 Cat. No.: G156792 Peso molecular: 342.30(Anhydrous) Beilstein Registry Number: 17(3/4)3008

GRADE & PURITY ≥99%(HPLC)

Synonyms

Galactinol | 1-alpha-D-Galactosyl-myo-inositol | O-alpha-D-galactosyl-(1->3)-1D-myo-inositol | GALACTINOL HYDRATE | WZE56L8UKR | 3-O-alpha-D-Galactosyl-1D-myo-inositol | alpha-D-galactosyl-(1->3)-1D-myo-inositol | 1-O-alpha-D-Galactosyl-D-myo-inositol | C

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Galactinol | 1-alpha-D-Galactosyl-myo-inositol | O-alpha-D-galactosyl-(1->3)-1D-myo-inositol | GALACTINOL HYDRATE | WZE56L8UKR | 3-O-alpha-D-Galactosyl-1D-myo-inositol | alpha-D-galactosyl-(1->3)-1D-myo-inositol | 1-O-alpha-D-Galactosyl-D-myo-inositol | C

Especificaciones y pureza

≥99%(HPLC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥99%(HPLC)

Nombres e identificadores

• Pubchem Sid: 504766676
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504766676
• Sonrisas canónicas: C(C1C(C(C(C(O1)OC2C(C(C(C(C2O)O)O)O)O)O)O)O)O
• IUPAC Name: (1S,2R,4S,5S)-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexane-1,2,3,4,5-pentol
• InChIKey: VCWMRQDBPZKXKG-ZNVDUFQESA-N
• INCHI: 1S/C12H22O11/c13-1-2-3(14)4(15)10(21)12(22-2)23-11-8(19)6(17)5(16)7(18)9(11)20/h2-21H,1H2/t2-,3+,4+,5?,6-,7+,8+,9+,10-,11?,12-/m1/s1
• Isómeros SMILES: C([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)OC2[C@H]([C@H](C([C@H]([C@@H]2O)O)O)O)O)O)O)O)O
• Peso molecular: 342.30(Anhydrous)
• Beilstein: 17(3/4)3008
• Reaxy-Rn: 62158499
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=62158499&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Cyclohexanols Oxanes Monosaccharides Cyclitols and derivatives Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: O-glycosyl compound - Cyclohexanol - Oxane - Monosaccharide - Cyclitol or derivatives - Cyclic alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water
• Sensibilidad: Hygroscopic
• Rotación específica [α]: 132° (C=1,H2O)
• Punto de fusión (°C): 221 °C
• Peso molecular: 342.300 g/mol
• XLogP3: -5.300
• Hydrogen Bond Donor Count: 9
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 3
• Exact Mass: 342.116 Da
• Monoisotopic Mass: 342.116 Da
• Topological Polar Surface Area: 201.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 379.000
• 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: 1

Referencias

1. Feng Lijuan, Yu Shuping, Jin Weimei, Xiao Changyan, Qiao Yan, Yang Guangfeng.  (2024)  The role of hydroponic solution of Ulva fasciata in modulating the antibiotic resistance of Vibrio alginolyticus.  JOURNAL OF APPLIED MICROBIOLOGY,      [PMID:39533112] [10.1093/jambio/lxae281]