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  1. Home
  3. Triclinic Polymorph Of 1-hy-droxy-cyclo-hexa-necarb-oxy-lic Acid.
  1. Home
  3. Triclinic Polymorph Of 1-hy-droxy-cyclo-hexa-necarb-oxy-lic Acid.

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Triclinic polymorph of 1-hy-droxy-cyclo-hexa-necarb-oxy-lic acid.

Lubabalo Ndima1, Eric Cyriel Hosten1, Richard Betz1

  • 1Nelson Mandela University, Summerstrand Campus, Department of Chemistry, University Way, Summerstrand, PO Box 77000, Port Elizabeth, 6031, South Africa.

Iucrdata
|January 19, 2026

View abstract on PubMed

Summary
This summary is machine-generated.

This study characterizes C7H12O3, an alpha-hydroxy-carboxylic acid. Molecular analysis reveals hydrogen bonds forming sheet-like structures in its crystal lattice.

Keywords:
crystal structurepolymorph

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Acidity of Terminal Alkynes: Formation of Acetylide Anions
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Acidity of Terminal Alkynes: Formation of Acetylide Anions
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Area of Science:

  • Crystallography
  • Organic Chemistry
  • Materials Science

Background:

  • Alpha-hydroxy-carboxylic acids are organic compounds with diverse applications.
  • Understanding the crystal structure of such compounds is crucial for predicting their physical and chemical properties.

Purpose of the Study:

  • To elucidate the crystal structure of the title compound, C7H12O3.
  • To investigate the intermolecular interactions governing its solid-state arrangement.

Main Methods:

  • Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.
  • Analysis of hydrogen bonding networks was performed.

Main Results:

  • The asymmetric unit contains two molecules of C7H12O3.
  • O-H⋯O hydrogen bonds were identified as the primary intermolecular force.
  • These hydrogen bonds organize the molecules into sheets perpendicular to the b axis.

    • Conclusions:

    • The crystal structure of C7H12O3 is characterized by sheet-like arrangements driven by hydrogen bonding.
    • This structural insight is fundamental for potential applications in materials science and organic synthesis.