This is an old revision of this page, as edited by Plasmic Physics (talk | contribs) at 09:47, 4 September 2011 (←Created page with '{{Chembox | SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:2...'). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 09:47, 4 September 2011 by Plasmic Physics (talk | contribs) (←Created page with '{{Chembox | SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:2...')(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)| Names | |
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| Systematic IUPAC name
Azanyl (substitutive) Dihydridonitrogen(•) (additive) | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| PubChem CID | |
| CompTox Dashboard (EPA) | |
InChI
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SMILES
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| Properties | |
| Chemical formula | NH 2 |
| Molar mass | 16.0226 g mol |
| Thermochemistry | |
| Std molar entropy (S298) |
194.71 J K mol |
| Std enthalpy of formation (ΔfH298) |
190.37 kJ mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references | |
The azanyl radical, NH
2, is the neutral form of the amide ion (NH
2). Azanyl radicals are highly reactive and consequently short lived; however, they form an important part of radical chemistry. In sufficiently high concentration, azanyl dimerises to form hydrazine.
References
- ^ "aminyl (CHEBI:29318)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute. IUPAC Names.