Structure via PubChem · Public domain (PubChem)
allylamine
Sign in to saveAllylamine is an organic compound with the formula C3H5NH2. This colorless liquid is the simplest stable unsaturated amine.
Chemical data
- Formula
- C3H7N
- Molecular weight
- 57.09 g/mol
- IUPAC name
- prop-2-en-1-amine
- SMILES
- C=CCN
- InChIKey
- VVJKKWFAADXIJK-UHFFFAOYSA-N
- XLogP
- 0.1
- Polar surface area
- 26 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
2,734 papers- Allylamine antifungal drugs.Current topics in medical mycology · 1992
- Poly(allylamine)-tripolyphosphate Ionic Assemblies as Nanocarriers: Friend or Foe?ACS applied bio materials · 2023
- Allylamine cardiotoxicity: metabolism and mechanism.Advances in experimental medicine and biology · 1983
- Naftifine: A Topical Allylamine for Superficial Dermatophytosis.The Journal of the Association of Physicians of India · 2023
- Allylamine cardiovascular toxicity.Toxicology · 1987
via PubMed
Wikidata facts
- Subclass of
- amine
- Mass
- 57.058
- Autonomy
- 374
Show 15 more facts
- chemical formula
- C₃H₇N
- canonical SMILES
- C=CCN
- pKa
- 9.49
- density
- 0.758
- melting point
- -88
- boiling point
- 54
- refractive index
- 1.4205
- phase point
- critical point
- electric dipole moment
- 1.2
- flash point
- -29
- lower flammable limit
- 2.2
- upper flammable limit
- 20
- partition coefficient water/octanol
- 0.03
- Commons category
- Allylamine
- ionization energy
- 8.76
via Wikidata · CC0
~1 min read
Encyclopedic overview
5 sectionsContents
- Production and reactions
- Other allylamines
- Safety
- References
- External links
Allylamine is an organic compound with the formula C3H5NH2. This colorless liquid is the simplest stable unsaturated amine.
==Production and reactions== All three allylamines, mono-, di-, and triallylamine, are produced by the treating allyl chloride with ammonia followed by distillation. Or by the reaction of allyl chloride with hexamine. Pure samples can be prepared by hydrolysis of allyl isothiocyanate. It behaves as a typical amine.
Excerpted from Wikipedia’s “allylamine” article, available under the CC BY-SA 4.0 licence.