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| SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:29318)|work = Chemical Entities of Biological Interest (ChEBI)|location = UK|publisher = European Bioinformatics Institute|at = IUPAC Names}}</ref> (substitutive)<br /> | | SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:29318)|work = Chemical Entities of Biological Interest (ChEBI)|location = UK|publisher = European Bioinformatics Institute|at = IUPAC Names}}</ref> (substitutive)<br /> | ||
Dihydridonitrogen(•)<ref name = "aminyl (CHEBI:29318)" /> (additive) | Dihydridonitrogen(•)<ref name = "aminyl (CHEBI:29318)" /> (additive) |
Revision as of 06:31, 9 September 2011
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
| |
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). Y verify (what is ?) 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.
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