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- Nitro compounds are organic compounds that contain one or more nitro functional groups (−NO<sub>2</sub>). [[Category:Organic compounds]]19 members (3 subcategories, 0 files) - 07:40, 29 August 2018
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- ...°C-73°C. It has the characteristic slightly sweet smell of nitroaromatic compounds, though it is toxic and inhalation of the dust should be avoided. It has a [[Category:Chemical compounds]]4 KB (458 words) - 20:56, 2 December 2018
- ...al water'''") also known as '''aqua regis''' ("'''king's water'''"), or '''nitro-hydrochloric acid''' is a highly corrosive fuming mixture of [[Nitric acid| ...are in trace amounts. Aqua regia will react extremely violent with organic compounds in sufficient quantities, sometimes with explosive results.3 KB (488 words) - 19:16, 12 March 2021
- ...ts [[wikipedia:Nitrovasodilator|vasodilation]] effects, which is where the nitro group in the nitrated alcohol causes the body to widen blood vessels, resul [[Category:Chemical compounds]]5 KB (611 words) - 20:03, 25 October 2020
- ...hols. Similarly, it converts amide, azide, imine, nitrile, nitro and oxime compounds into amines. LAH is most commonly used for the reduction of esters and carb The byproducts or neutralizing LAH are lithium and aluminium compounds, usually lithium hydroxide or carbonate and aluminium oxide. They can eithe6 KB (799 words) - 17:39, 29 February 2020
- ...e quality. The theoretical maximum is 14.15% N, which corresponds to three nitro groups per glucose unit. [[Category:Chemical compounds]]7 KB (995 words) - 15:26, 4 March 2019
- | OtherNames = 1,2,3-Tris(nitrooxy)propane<br>Glyceryl trinitrate<br>Nitro-dur<br>Nitroglycerol<br>Nitrostat<br>Trinitroglycerin<br>Trinitroglycerine ...[[diatomaceous earth]]), to make it stable. Most smokeless powders contain nitro. Extracting the nitroglycerin from these products however, is impractical a7 KB (807 words) - 12:55, 27 February 2024
- | OtherNames = Nitro fuel<br>Nitrocarbol ...cal formula '''CH<sub>3</sub>NO<sub>2</sub>'''. It is the simplest organic nitro compound.10 KB (1,375 words) - 20:01, 16 May 2023
- ...as '''dinitrogen monoxide''', '''nitrogen protoxide''', '''nitrous''', '''nitro''', '''NOS''' or more popular '''laughing gas''' is a chemical compound wit [[Category:Chemical compounds]]6 KB (801 words) - 17:05, 8 January 2020
- ...ed in the usual way. However there are many chemicals, such as heavy metal compounds or organic solvents, that require '''special disposal techniques'''. In the ...nd soluble heavy metal compounds, it's best to convert them into insoluble compounds, which are less toxic.347 KB (46,057 words) - 20:09, 13 March 2024
- [[Category:Chemical compounds]] [[Category:Organic compounds]]9 KB (1,159 words) - 09:31, 23 September 2023
- ...ich leaves Cl<sup>-</sup> ions behind which can easily attack many organic compounds. However, the [[sulfate]] ions left behind by the dissociation of sulfuric * Preparation of nitro compounds through [[nitration]]27 KB (4,285 words) - 21:31, 9 September 2023
- | IUPACName = 1-Methyl-2-nitro-benzene | SystematicName = 1-Methyl-2-nitro-benzene5 KB (566 words) - 15:45, 28 December 2023
- ...rolyzed to an aldehyde. It can also be used to selectively reduce aromatic nitro groups to anilines. *Reduce aromatic nitro groups to anilines7 KB (895 words) - 15:11, 18 November 2023
- ...,3,4-tetrakis-nitrooxy-butane<br>Erythrityl tetranitrate<br>ETN<br>Tetra-O-nitro-erythritol ...due to being a strong vasodilator, property seen in other nitrated organic compounds.6 KB (734 words) - 19:52, 31 August 2022
- [[Category:Chemical compounds]] [[Category:Organic compounds]]5 KB (660 words) - 22:12, 26 October 2020
- Nitroamines are organic compounds which contain the functional group R<sub>2</sub>N-NO<sub>2</sub>. They are [[Category:Nitrogen compounds]]9 members (0 subcategories, 0 files) - 15:03, 8 August 2019
- ...have the molecular structure R-ONO. Alkyl nitrites are distinct from nitro compounds (R-NO<sub>2</sub>). [[Category:Organic compounds]]1 member (0 subcategories, 0 files) - 17:30, 3 July 2016
- '''Nitroalkanes''' are aliphatic organic compounds which contain at least one nitro functional groups (-NO<sub>2</sub>). [[Category:Nitro compounds]]2 members (0 subcategories, 0 files) - 08:11, 29 August 2018
- | IUPACName = Sodium (4Z)-4-[(1-hydroxynaphthalen-2-yl)hydrazinylidene]-7-nitro-3-oxonaphthalene-1-sulfonate | PIN = Sodium 1-[1-Hydroxynaphthylazo]-6-nitro-2-naphthol-4-sulfonate5 KB (559 words) - 13:20, 26 November 2022
- [[Category:Organic compounds]] [[Category:Aromatic compounds]]4 KB (488 words) - 21:06, 2 February 2020