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Updated: Jun 5, 2026

A Strategy for Sensitive, Large Scale Quantitative Metabolomics
Published on: May 27, 2014
1-De-oxy-d-galactitol (l-fucitol)
1-Deoxy-d-galactitol forms crystalline layers stabilized by extensive hydrogen bonds. Each molecule participates in five hydrogen bonds, influencing its crystal structure and properties.
Area of Science:
- Crystallography
- Molecular structure
- Hydrogen bonding
Background:
- 1-Deoxy-d-galactitol is a sugar alcohol with potential biological relevance.
- Understanding its crystalline structure is key to elucidating its physical and chemical properties.
Purpose of the Study:
- To determine the crystal structure of 1-Deoxy-d-galactitol.
- To characterize the hydrogen bonding network within its crystalline form.
Main Methods:
- Single-crystal X-ray diffraction analysis was employed.
- The arrangement of molecules and hydrogen bonds in the crystal lattice was analyzed.
Main Results:
- 1-Deoxy-d-galactitol crystallizes in layers parallel to the ac plane.
- Each molecule engages in five hydrogen bonds, acting as both donor and acceptor.
- The observed hydrogen bonding network dictates the molecular packing in the crystal.
Conclusions:
- The crystalline structure of 1-Deoxy-d-galactitol is characterized by extensive intermolecular hydrogen bonding.
- This hydrogen bonding network is crucial for the stability and organization of the crystal lattice.
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