Structure via PubChem · Public domain (PubChem)
پارالدهید
Sign in to saveAlso known as Paral, paracetaldehyde, acetaldehyde trimer, paraacetaldehyde, 2,4,6-trimethyl-s-trioxane, 1,3,5-trimethyl-2,4,6-trioxane, Paraldehyde, 2,4,6-trimethyl-1,3,5-trioxane
Paraldehyde is the cyclic trimer of acetaldehyde molecules. Formally, it is a derivative of 1,3,5-trioxane, with a methyl group substituted for a hydrogen atom at each carbon. The corresponding tetramer is metaldehyde. A colourless liquid, it is sparingly soluble in water and highly soluble in ethanol. Paraldehyde slowly oxidizes in air, turning brown and producing an odour of acetic acid. It attacks most plastics and rubbers and should be kept in glass bottles.
Chemical data
- Formula
- C6H12O3
- Molecular weight
- 132.16 g/mol
- IUPAC name
- 2,4,6-trimethyl-1,3,5-trioxane
- SMILES
- CC1OC(OC(O1)C)C
- InChIKey
- SQYNKIJPMDEDEG-UHFFFAOYSA-N
- XLogP
- 0.7
- Polar surface area
- 27.7 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Research
577 papers- Paraldehyde.Journal of applied toxicology : JAT · 1991
- Paraldehyde acidosis.The American journal of medicine · 1967
- Paraldehyde.The Hospital · 1893
- [Paraldehyde].The Canadian nurse · 1948
- Eclampsia.Clinics in obstetrics and gynaecology · 1982
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 132.078644
- Has use
- medication
Show 10 more facts
- melting point
- 12.6
- chemical formula
- C₆H₁₂O₃
- Commons category
- Paraldehyde
- electric dipole moment
- 1.43
- World Health Organisation international non-proprietary name
- paraldehyde
- canonical SMILES
- CC1OC(OC(O1)C)C
- isomeric SMILES
- C[C@@H]1O[C@@H](OC(O1)C)C
- different from
- paraformaldehyde
- described by source
- Encyclopædia Britannica 11th edition
- boiling point
- 124.35
via Wikidata · CC0