ethylene glycol
Ethylene glycol is an organic compound with the formula C₂H₆O₂. It is a clear, colorless, syrupy liquid with a sweet taste — but highly toxic if ingested.
Key facts
Common uses
Primary ingredient in antifreeze and engine coolants
Used as a precursor in manufacturing polyester fibers and PET plastics
Acts as a dehydrating agent in various industrial processes
Physical properties
Boiling point: ~197 °C
Melting point: −12.9 °C
Miscible with water
Viscous and hygroscopic (absorbs water)
Toxicity
Ingestion can cause severe metabolic acidosis, kidney failure, and can be fatal
Metabolized to glycolic acid and oxalic acid, which cause organ damage
Requires prompt medical treatment (e.g., fomepizole)
Why it’s in antifreeze
Lowers the freezing point and raises the boiling point of water
Helps prevent engine coolant from freezing in winter and overheating in summer
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Description
Ethylene glycol is an organic compound with the formula C₂H₆O₂. It is a clear, colorless, syrupy liquid with a sweet taste — but highly toxic if ingested.
Key facts
Common uses
Primary ingredient in antifreeze and engine coolants
Used as a precursor in manufacturing polyester fibers and PET plastics
Acts as a dehydrating agent in various industrial processes
Physical properties
Boiling point: ~197 °C
Melting point: −12.9 °C
Miscible with water
Viscous and hygroscopic (absorbs water)
Toxicity
Ingestion can cause severe metabolic acidosis, kidney failure, and can be fatal
Metabolized to glycolic acid and oxalic acid, which cause organ damage
Requires prompt medical treatment (e.g., fomepizole)
Why it’s in antifreeze
Lowers the freezing point and raises the boiling point of water
Helps prevent engine coolant from freezing in winter and overheating in summer..
Industrial Routes to Ethylene Glycol (High-Level Overview)
1. Oxidation of Ethylene → Ethylene Oxide → Ethylene Glycol
This is the main commercial process today.
Ethylene is partially oxidized with oxygen using a silver-based catalyst to form ethylene oxide (EO).
Ethylene oxide is then hydrated with water to produce ethylene glycol along with some higher glycols.
This method is efficient and used worldwide in large-scale chemical plants.
2. Hydrolysis of Ethylene Oxide Under Acidic or Neutral Conditions
Ethylene oxide reacts with excess water to produce ethylene glycol.
More water shifts the reaction toward glycol rather than di- or tri-ethylene glycol.
Carried out in controlled industrial reactors.
3. Alternative Routes (Less Common)
Carbonylation of formaldehyde followed by hydrogenation
Direct synthesis from syngas (CO + H₂) via intermediate steps
Biobased approaches, such as fermenting biomass-derived sugars, then catalytic conversion to glycol
These are used where sustainable or non-petroleum pathways are desired.
Notes on Safety and Practicality
Ethylene glycol synthesis involves hazardous intermediates, especially ethylene oxide, which is flammable, carcinogenic, and explosive. As such, synthesis is performed only in industrial facilities with specialized equipment.










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