D-Glucose 6-phosphate - ≥95% , CAS No.56-73-5

CAS: 56-73-5 Cat. No.: D1518225 Molecular Weight: 260.14 EC Number: 200-286-9 PubChem CID: 439958

GRADE & PURITY ≥95%

Synonyms

(2R,3R,4S,5R)-2,3,4,5-Tetrahydroxy-6-oxohexyl dihydrogen phosphate

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

D-Glucose 6-phosphate is a glucose sugar phosphorylated at the hydroxy group on carbon 6.

Specifications

Synonyms

(2R, 3R, 4S, 5R)-2, 3, 4, 5-Tetrahydroxy-6-oxohexyl dihydrogen phosphate

Specifications & Purity

≥95%

Storage

Protected from light, Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Canonical Smiles: C(C(C(C(C(C=O)O)O)O)O)OP(=O)(O)O
• IUPAC Name: [(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl] dihydrogen phosphate
• InChIKey: VFRROHXSMXFLSN-SLPGGIOYSA-N
• INCHI: 1S/C6H13O9P/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14/h1,3-6,8-11H,2H2,(H2,12,13,14)/t3-,4+,5+,6+/m0/s1
• Isomeric SMILES: C([C@H]([C@H]([C@@H]([C@H](C=O)O)O)O)O)OP(=O)(O)O
• PubChem CID: 439958
• Molecular Weight: 260.14

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Monosaccharide phosphates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Monosaccharide phosphates
• Alternative Parents: Monoalkyl phosphates Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monosaccharide phosphate - Monoalkyl phosphate - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit.
• External Descriptors: D-glucose 6-phosphate

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

Chemical and Physical Properties

• Sensitivity: Moisture sensitive
• Molecular Weight: 260.140 g/mol
• XLogP3: -4.500
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 7
• Exact Mass: 260.03 Da
• Monoisotopic Mass: 260.03 Da
• Topological Polar Surface Area: 165.000 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 263.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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

References

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2. Jiang Zhu, Jing Feng, Kai Tian, Chong Li, Mei Li, Xinghui QIU.  (2022)  Functional characterization of CYP6G4 from the house fly in propoxur metabolism and resistance.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:36127048] [10.1016/j.pestbp.2022.105186]

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7. Zhiye Yan, Weiwei Tang, Bin Li.  (2025)  Expanding Metabolome Coverage in LC–MS/MS Analysis through Hydralazine-Based Multifunctional Derivatization.  ANALYTICAL CHEMISTRY,      [PMID:41277254] [10.1021/acs.analchem.5c02101]

8. Yuhan Zhao, Xiaojie Zhou, Mei Li, Xinghui Qiu.  (2025)  Aedes albopictus CYP6Z8 metabolizes multiple AChE-inhibiting insecticides.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:41629003] [10.1016/j.pestbp.2025.106934]

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