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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 eithe
    6 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 a
    7 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-benzene
    5 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 anilines
    7 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
  • | 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-sulfonate
    5 KB (559 words) - 13:20, 26 November 2022
  • [[Category:Organic compounds]] [[Category:Aromatic compounds]]
    4 KB (488 words) - 21:06, 2 February 2020
  • '''Peroxide forming chemicals''' are a group of chemical compounds capable of forming very sensitive peroxides if exposed to atmospheric [[oxy ...de or some other form of peroxide are not included in this group, as these compounds require an already existing peroxide and do not form such peroxides in cont
    13 KB (1,730 words) - 14:06, 9 August 2023
  • ...]s, [[aldehyde]]s, [[amine]]s, [[ester]]s, [[halocarbons]], [[ketone]]s, [[nitro compound]]s, but are stable and soluble in ''very'' dry organic solvents, l ...organometallic compounds, having an inert environment is crucial, as many compounds are air-sensitive
    6 KB (857 words) - 14:37, 1 April 2019
  • ...tion''' is a general class of chemical processes for the introduction of a nitro group into an organic chemical compound. ...ructure of nitro compounds and nitrates is that the nitrogen atom in nitro compounds is directly bonded to a non-oxygen atom, typically carbon or another nitrog
    4 KB (524 words) - 16:18, 14 April 2020
  • ...ens, allows them to substitute for halogens in several classes of chemical compounds. .../sub> || — || [[dinitrogen tetroxide]] || [[nitrous acid]] || nitrite || nitro- || -yl nitrite
    4 KB (399 words) - 20:19, 6 September 2022
  • | OtherNames = N-nitroguanidine<br>Nitro-guanidine<br>NQ<br>Picrite [[Category:Chemical compounds]]
    5 KB (594 words) - 22:43, 28 December 2020
  • ...ef> Sodium borate in glacial acetic acid will also oxidize oximes to nitro compounds. *Make aromatic nitro compounds
    6 KB (655 words) - 15:25, 30 November 2018
  • ...ts with an [[aldehyde]] or [[ketone]] in the presence of a base to form β-nitro alcohols, which can be further dehydrated to yield nitroalkenes, nitroketon ...36; (1903); p. 711</ref> DMDO can also be used to oxidize amines to nitro compounds.
    7 KB (850 words) - 22:48, 20 January 2020
  • ...ctional groups. For example, DMDO will oxidize primary [[amine]]s to nitro compounds and sulfides to sulfoxides. DMDO can also be used to convert nitro compounds to carbonyl compounds (Nef reaction).
    4 KB (481 words) - 12:00, 24 December 2022
  • Silver nitrite will react with haloalkanes to give nitro compounds. *Preparation of aniline compounds
    4 KB (426 words) - 22:05, 11 June 2023
  • ...ears prior that couples two carbonyl compounds to form β-hydroxy carbonyl compounds known as "aldols" (aldehyde and alcohol). ...he alkoxide by the previously protonated base will yield the respective β-nitro alcohol as product.
    2 KB (269 words) - 21:22, 10 August 2020
  • '''Nitro compounds''' are organic compounds that contain one or more nitro functional groups (−NO<sub>2</sub>). ...n be acidic. For similar reasons, the presence of nitro groups in aromatic compounds retards electrophilic aromatic substitution but facilitates nucleophilic ar
    6 KB (839 words) - 21:28, 26 October 2020
  • ...e esters of nitrous acid and contain the nitrosoxy functional group. Nitro compounds contain the C–NO<sub>2</sub> group. Nitrites have the general formula RON
    3 KB (473 words) - 00:51, 29 March 2020
  • Unlike other aromatic energetic compounds, styphnic acid cannot be safely burned as it may explode. [[Category:Chemical compounds]]
    6 KB (671 words) - 19:33, 16 May 2023
  • ...osive, based on the basic six-carbon [[benzene]] ring structure with three nitro functional groups (NO<sub>2</sub>) and three [[amine]] (NH<sub>2</sub>) gro Like nitroaromatic compounds, TATB is harmful if ingested and will stain the skin yellow.
    6 KB (753 words) - 22:08, 26 October 2020
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    8 KB (913 words) - 19:47, 11 October 2020
  • ...o the public and when available it's more expensive than similar explosive compounds. *Make colored compounds
    5 KB (559 words) - 19:47, 25 October 2020
  • FOX-7 is a powerful explosive and like all nitro compounds it must be handled with care. [[Category:Chemical compounds]]
    8 KB (1,066 words) - 11:49, 28 December 2020
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    4 KB (476 words) - 22:33, 28 December 2020
  • ...ide. As such, it does not reduce amides, ethers, lactones, nitriles, nitro compounds and epoxides. [[Category:Chemical compounds]]
    6 KB (625 words) - 21:17, 30 August 2022
  • | OtherNames = Penta-O-nitro-xylitol<br>XPN ...due to being a strong vasodilator, property seen in other nitrated organic compounds.
    6 KB (661 words) - 21:07, 31 August 2022
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    5 KB (539 words) - 00:15, 6 November 2023