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CAS 69984-73-2

Nonyl beta-D-Glucopyranoside TCI N0909

Nonyl beta-D-Glucopyranoside TCI N0909

Chemical Identity

CAS No.
69984-73-2
PubChem
CID 113558·SID 160870976
Formula
C15H30O6
Molecular weight
306.39 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(hydroxymethyl)-6-nonoxyoxane-3,4,5-triol
SMILES
CCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
InChIKey
QFAPUKLCALRPLH-UHFFFAOYSA-N
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Nonyl beta-D-Glucopyranoside is a chemical compound widely used in laboratory experiments across chemical and biochemical research. As a non-ionic surfactant, it plays a crucial role in solubilizing lipids and proteins, making it essential for various analytical techniques. Its ability to facilitate extraction and precipitation processes enhances the efficiency of experimental workflows. This compound is particularly valuable in biophysical studies where precise molecular interactions are required. It is commonly found in research settings where stability and reliability are paramount.

The compound's non-ionic nature makes it a preferred choice for many applications. Unlike ionic surfactants, it does not produce negative or positive ions, thus avoiding interference with other chemical reactions. This property ensures that it remains stable under a wide range of environmental conditions. Additionally, its resistance to degradation in solution prolongs its shelf life and enhances the accuracy of experimental results. These characteristics make it an ideal component for both routine and advanced laboratory procedures.

In Indonesian laboratories, Nonyl beta-D-Glucopyranoside is frequently used in biochemical, pharmacological, and food technology research. Researchers and students at universities and research institutions rely on this compound for experiments requiring non-ionic surfactants. Its versatility and reliability have made it a standard material in various scientific disciplines, supporting both fundamental and applied research efforts.

  • Biochemical research utilizes Nonyl beta-D-Glucopyranoside for solubilizing membrane proteins, aiding in structural analysis and functional studies.
  • Pharmaceutical development benefits from its ability to stabilize and dissolve hydrophobic compounds, enhancing drug formulation processes.
  • Food technology applications leverage its surfactant properties to improve emulsification and solubility in food product development.
  • Spectroscopic analysis relies on this compound to enhance the clarity and accuracy of molecular structure determination.
  • Cell membrane studies use it to maintain membrane integrity during extraction and purification procedures.

Brand TCI
CAS number 69984-73-2
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Glycoscience
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid powder
Storage Store in a cool, dry place away from direct sunlight

Nonyl beta-D-Glucopyranoside should be stored in a cool, dry environment to maintain its chemical integrity. It is best kept in airtight containers to prevent moisture absorption, which could affect its performance. Since it is a solid powder, it should be handled with care to avoid inhalation or skin contact. In laboratory settings, it is advisable to use a fume hood when working with larger quantities to ensure proper ventilation. Always follow standard safety protocols when handling chemical substances to minimize risks. Proper storage and handling ensure the compound remains effective and safe for use in various research applications.

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