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Molecular compound · triol

Glycerol

C₃H₈O₃

Glycerol is C₃H₈O₃, a three-carbon triol. Its condensed structure HOCH₂–CHOH–CH₂OH places one hydroxyl group on each carbon.

Name note: glycerol is the compound name; glycerin/glycerine is often used for glycerol-containing commercial material and can include water or impurities.
Essentials

Three –OH groups define glycerol as a triol.

The condensed structure is much more informative than C₃H₈O₃ because it shows one hydroxyl group on each carbon of the three-carbon chain.

Condensed glycerol structure HO-CH2-CH(OH)-CH2-OH
Beginner view: a three-carbon chain carrying three hydroxyl groups.
Polyol

More than one alcohol group can exist in one molecule.

Glycerol is a triol because it has three alcohol functional groups.

Detail

The 2D structure fixes the chain connectivity while leaving conformations free.

Single C–C and C–O bonds allow many three-dimensional conformations; the flat drawing is a connectivity map, not a rigid molecular pose.

Source-derived two-dimensional structure of glycerol
Reference connectivity for propane-1,2,3-triol.
Flexibility

Three hydroxyl groups do not lock the molecule flat.

Rotation about single bonds produces many conformations while preserving connectivity.

Read the formula

C3H8O3 is a compact statement of composition.

Subscripts count atoms in the chemical molecule. Atom percentages and mass percentages answer different questions because the constituent elements have different atomic masses.

3 Ccarbon atoms
8 Hhydrogen atoms
3 Ooxygen atoms

Percentages are calculated from standard relative atomic masses and rounded for display.

Understand

Multiple –OH groups create many hydrogen-bonding opportunities.

Each hydroxyl can participate in donor and acceptor interactions, producing a dense intermolecular hydrogen-bond network in glycerol and in mixtures with water.

Three hydroxyl groups highlighted as hydrogen-bonding sites in glycerol
The visual counts interaction sites without pretending every molecule always has the same fixed number of hydrogen bonds.
Structure → viscosity

Strong, numerous intermolecular interactions resist molecular rearrangement.

Hydrogen bonding is one major contributor to glycerol's high viscosity, alongside molecular size and shape.

Reference identifiers

Names and identifiers that pin down the chemical identity.

FormulaC₃H₈O₃
CAS Registry Number56-81-5
PubChem CID753
Advanced

Push past the first model without losing the simple picture.

Is glycerol chiral?

Unsubstituted glycerol is achiral because the two terminal CH₂OH groups are equivalent.

Does three –OH groups mean three times the hydrogen bonding of methanol?

No. Interaction counts and strengths are not linearly additive; geometry, concentration and network organization matter.

Is glycerin always chemically pure glycerol?

Not necessarily. Commercial naming can refer to glycerol-rich material with specified water or impurity content.

Constituent elements

Connect the compound back to the periodic table.