Cas no 33068-18-7 (D-Mannose-6-phosphate disodium salt hydrate)

D-Mannose-6-phosphate disodium salt hydrate is a phosphorylated monosaccharide derivative widely used in biochemical and glycobiology research. Its key advantages include high purity and stability, making it suitable for enzymatic studies, carbohydrate metabolism research, and glycoprotein synthesis. The disodium salt form enhances solubility in aqueous solutions, facilitating its use in buffer systems. As a hydrate, it ensures consistent handling and storage properties. This compound serves as a critical intermediate in metabolic pathways, particularly in glycosylation processes. Its well-defined structure allows for precise applications in mechanistic studies and inhibitor development. The product is commonly employed in analytical standards and as a substrate for kinases and phosphatases.
D-Mannose-6-phosphate disodium salt hydrate structure
33068-18-7 structure
Product Name:D-Mannose-6-phosphate disodium salt hydrate
CAS No:33068-18-7
MF:C6H11Na2O9P
MW:304.099445581436
MDL:MFCD00135857
CID:294021
PubChem ID:44120017
Update Time:2025-05-23

D-Mannose-6-phosphate disodium salt hydrate Chemical and Physical Properties

Names and Identifiers

    • D-Mannose,6-(dihydrogen phosphate), disodium salt (9CI)
    • D-MANNOSE 6-PHOSPHATE, DISODIUM SALT
    • D-Mannose-6-phosphate, Disodium Salt
    • AC1L3M25
    • AC1NFKFS
    • AC1Q1US6
    • AGN-PC-00Q1D0
    • CTK8F9314
    • disodium (3,4,5,6-tetrahydroxyoxan-2-yl)methyl phosphate
    • disodium 6-o-phosphonatohexopyranose
    • d-Mannose, 6-(dihydrogen phosphate), disodium salt
    • D-Mannose-6-phosphate disodium salt hydrate
    • D-Mannose 6-phosphate disodium salt hydrate
    • Sodium (2R,3R,4S,5S)-2,3,4,5-tetrahydroxy-6-oxohexyl phosphate
    • mannose-6-phosphate disodium
    • Q27252386
    • SCHEMBL2387370
    • MANNOSE, 6-(DIHYDROGEN PHOSPHATE), DISODIUM SALT, D-
    • UNII-1GAU7QN1V1
    • 1GAU7QN1V1
    • starbld0016600
    • D-MANNOSE, 6-(DIHYDROGEN PHOSPHATE), SODIUM SALT (1:2)
    • Disodium D-mannose 6-phosphate
    • 33068-18-7
    • D-Mannose 6-phosphate disodium salt
    • EINECS 251-366-5
    • D-MANNOSE 6-PHOSPHATE DISODIUM
    • D-Mannose 6-(phosphoric acid disodium) salt
    • D-Mannose 6-phosphate hydrate disodium salt
    • isodium,(3,4,5,6-tetrahydroxyoxan-2-yl)methylphosphate
    • MDL: MFCD00135857
    • Inchi: 1S/C6H13O9P.2Na/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);;/q;2*+1/p-2/t3-,4-,5-,6-;;/m1../s1
    • InChI Key: VQLXCAHGUGIEEL-OXIHULNRSA-L
    • SMILES: P(=O)([O-])([O-])OC[C@H]([C@H]([C@@H]([C@@H](C=O)O)O)O)O.[Na+].[Na+]

Computed Properties

  • Exact Mass: 303.994
  • Monoisotopic Mass: 303.994
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 266
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 5
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 170A^2

Experimental Properties

  • Color/Form: Not determined
  • Boiling Point: 564.1°Cat760mmHg
  • Flash Point: 295°C
  • Solubility: H2O: 50?mg/mL, clear, colorless
  • PSA: 180.22000
  • LogP: -2.38540
  • Solubility: water

D-Mannose-6-phosphate disodium salt hydrate Security Information

  • WGK Germany:3
  • Safety Instruction: 24/25
  • FLUKA BRAND F CODES:10-21
  • Storage Condition:?20°C

D-Mannose-6-phosphate disodium salt hydrate Customs Data

  • HS CODE:29400090

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Additional information on D-Mannose-6-phosphate disodium salt hydrate

D-Mannose-6-phosphate disodium salt hydrate: A Comprehensive Overview

D-Mannose-6-phosphate disodium salt hydrate, a compound with the CAS number 33068-18-7, is a widely recognized and utilized molecule in the field of biochemistry and pharmaceutical research. This compound, often referred to as D-Mannose-6-phosphate disodium salt hydrate, plays a crucial role in various biological pathways and has garnered significant attention due to its multifaceted applications.

The molecular structure of D-Mannose-6-phosphate disodium salt hydrate consists of a hexose sugar (mannose) phosphorylated at the 6-position, with the addition of two sodium ions and one water molecule in its hydrated form. This unique configuration imparts distinct chemical and biological properties, making it an invaluable component in synthetic biology, enzymology, and drug development.

One of the most notable applications of D-Mannose-6-phosphate disodium salt hydrate is in the context of glycosylation processes. Glycosylation is a fundamental post-translational modification that significantly influences the structure and function of proteins. This compound serves as a key intermediate in the synthesis of glycoproteins, which are essential for various cellular processes, including immune responses, cell signaling, and pathogen recognition.

Recent advancements in the field have highlighted the importance of D-Mannose-6-phosphate disodium salt hydrate in therapeutic interventions. For instance, studies have demonstrated its potential role in modulating immune responses by acting as a precursor for glycoprotein synthesis. This has opened up new avenues for developing vaccines and immunotherapies targeting infectious diseases and chronic conditions.

The compound's ability to interact with specific enzymes has also been explored in detail. Research has shown that D-Mannose-6-phosphate disodium salt hydrate can serve as a substrate for enzymes involved in glycosyltransferase pathways. These enzymes are critical for constructing complex carbohydrate structures on the surface of cells, which are often targeted by pathogens. By understanding and manipulating these pathways, researchers aim to develop novel strategies for preventing and treating infections.

In addition to its biological significance, D-Mannose-6-phosphate disodium salt hydrate has been investigated for its potential applications in regenerative medicine. Studies have suggested that this compound can promote cellular proliferation and differentiation, making it a promising candidate for tissue engineering and wound healing. The ability of D-Mannose-6-phosphate disodium salt hydrate to stimulate these processes is attributed to its influence on intracellular signaling pathways that regulate growth and repair mechanisms.

The pharmaceutical industry has also recognized the value of D-Mannose-6-phosphate disodium salt hydrate in drug development. Its structural properties make it an excellent candidate for use as a chiral building block in the synthesis of complex organic molecules. This has implications for developing new drugs with improved efficacy and reduced side effects. Furthermore, its role as an enzyme inhibitor has been explored in the context of treating metabolic disorders and cancer.

From an industrial perspective, D-Mannose-6-phosphate disodium salt hydrate is produced through controlled chemical reactions that ensure high purity and yield. The manufacturing process involves several steps, including phosphorylation of mannose followed by crystallization and hydration. These steps are carefully optimized to produce a product that meets stringent quality standards required for pharmaceutical applications.

The safety profile of D-Mannose-6-phosphate disodium salt hydrate is another critical aspect that has been extensively studied. Toxicology studies have demonstrated that this compound is well-tolerated at therapeutic doses, with minimal adverse effects. However, as with any biochemical compound, proper handling and storage conditions are essential to maintain its stability and efficacy.

The environmental impact of producing and using D-Mannose-6-phosphate disodium salt hydrate is also a consideration that researchers are addressing. Efforts are being made to develop more sustainable manufacturing processes that minimize waste generation and reduce energy consumption. Additionally, research is ongoing to explore alternative sources for mannose derivatives that could potentially reduce reliance on traditional agricultural practices.

In conclusion, D-Mannose-6-phosphate disodium salt hydrate is a versatile compound with significant applications across multiple domains of science and medicine. Its role in glycosylation processes, immune modulation, regenerative medicine, and drug development underscores its importance as a biochemical intermediate. As research continues to uncover new insights into its properties and functions, it is likely that this compound will remain at the forefront of innovation in biochemistry and pharmaceutical sciences.

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