869668-28-0

Basic information

• Product Name: 2-PROPYL-1-PENTYL MALTOPYRANOSIDE
• Synonyms: 2-PROPYL-1-PENTYL MALTOPYRANOSIDE;2-Propyl-1-Pentyl-β-D-Maltopyranoside
• CAS NO: 869668-28-0
• Molecular Formula: C20H38O11
• Molecular Weight: 454.51
• Mol File: 869668-28-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-PROPYL-1-PENTYL MALTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PROPYL-1-PENTYL MALTOPYRANOSIDE(869668-28-0)
• EPA Substance Registry System: 2-PROPYL-1-PENTYL MALTOPYRANOSIDE(869668-28-0)

Safety Data

• Hazardous Substances Data: 869668-28-0(Hazardous Substances Data)

Usage

Uses

Used in Research Applications:
2-Propyl-1-pentyl maltopyranoside is used as a research compound for its amphiphilic properties, which can be valuable in various scientific studies and experiments. Its ability to interact with both water and oil makes it a potential candidate for use in the development of new materials or processes.
Used in Manufacturing:
2-Propyl-1-pentyl maltopyranoside is used as a surfactant or detergent in manufacturing processes due to its amphiphilic properties. Its ability to interact with both water and oil can help improve the efficiency of cleaning or emulsifying processes, making it a useful component in the production of various products.
Used in Pharmaceutical Industry:
2-Propyl-1-pentyl maltopyranoside is used as a pharmaceutical excipient for its potential to enhance the solubility and stability of active pharmaceutical ingredients. Its amphiphilic nature may allow it to facilitate the delivery of drugs, improving their bioavailability and therapeutic effectiveness.
Used in Cosmetics Industry:
2-Propyl-1-pentyl maltopyranoside is used as an ingredient in cosmetic products for its potential to improve the texture and feel of formulations. Its amphiphilic properties may contribute to the creation of more effective and pleasant-to-use products, enhancing the overall consumer experience.

Upstream product

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Relevant articles and documents

Synthetic studies on selectin ligands/lnhibitors. Synthesis and biological evaluation of sulfated and phosphorylated β-D-galacto- and lactopyranosides containing fatty-alkyl residues of different carbon chain lengths

To investigate the biological selectin-ligand interactions, fourteen sulfated and eight phosphorylated β-D-galacto- and lactopyranosides containing branched fatty-alkyl residues in place of the ceramide have been synthesized. Regioselective sulfation of the parent glycolipids through the dibutylstannylene acetal with a certain amount of sulfur trioxide- trimethylamine complex produced the target sulfated glycolipids, while stepwise phosphorylation by treatment of the properly protected diol with dibenzyloxy(diisopropylamino)phosphine gave the phosphorylated glycolipids. The synthetic glycolipids showed an interesting mode of inhibition of the binding of HL-60 cells to immobilized P-, L- and E-selectins during in vitro experiments. In addition, using computer modeling techniques, we examined the molecular basis for the ligand-selectin complex formation. These glycolipids may be useful as therapeutic agents against selectin-dependent inflammation.