Research
28,120 papers- Azide-Modified Nucleosides as Versatile Tools for Bioorthogonal Labeling and Functionalization.Chemical record (New York, N.Y.) · 2022
- Azide rearrangements in electron-deficient systems.Chemical Society reviews · 2006
- Metabolic activation of the mutagen azide in biological systems.Mutation research · 1988
- Azide-Terminated RAFT Polymers for Biological Applications.Current protocols in chemical biology · 2020
- Photoactivatable Fluorogenic Azide-Alkyne Click Reaction: A Dual-Activation Fluorescent Probe.Chemistry, an Asian journal · 2022
via PubMed
Wikidata facts
- Image
- Azide-2D.svg
Show 4 more facts
- topic has template
- Template:Azides
- Commons category
- Azides
- topic's main category
- Category:Azides
- SMARTS notation
- [$([$(*-[NX2-]-[NX2+]#[NX1]),$(*-[NX2]=[NX2+]=[NX1-])]),$([$([NX1-]=[NX2+]=[NX1-]),$([NX1]#[NX2+]-[NX1-2])])]
via Wikidata · CC0
~9 min read
Encyclopedic overview
15 sectionsContents
- Preparation
- Bonding
- Reactions
- Redox behaviour and trend to disproportionation
- Destruction by oxidation by nitrite
- Applications
- Primary explosives and propellants
- Microbial inhibitor and undesirable side effects
- Purification of molten sodium
- Click chemistry
- Other uses
- Safety
- See also
- References
- External links
thumb|The azide anion
In chemistry, azide (, ) is a linear, polyatomic anion with the formula and structure . It is the conjugate base of hydrazoic acid . Organic azides are organic compounds with the formula , containing the azide functional group. The dominant application of azides is as a propellant in air bags.
Excerpted from Wikipedia’s “azide” article, available under the CC BY-SA 4.0 licence.