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Silver nitrite

From Wikipedia, the free encyclopedia
Silver nitrite
Silver nitrite
Silver nitrite
Names
IUPAC name
Silver(I) nitrite
Other names
Argentous nitrite
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.029.128Edit this at Wikidata
EC Number
  • 232-041-7
UNII
  • InChI=1S/Ag.HNO2/c;2-1-3/h;(H,2,3)/q+1;/p-1
    Key: KKKDGYXNGYJJRX-UHFFFAOYSA-M
  • N(=O)[O-].[Ag+]
Properties
AgNO2
Molar mass153.87 g/mol
Appearancecolorless to yellow crystals
Melting point140 °C (284 °F; 413 K)
0.155 g/100 mL (0 °C)
0.275 g/100 mL (15 °C)
1.363 g/100 mL (60 °C)
Solubilityinsoluble inethanol
−42.0·10−6 cm3/mol
Hazards
GHS labelling:[1]
GHS03: OxidizingGHS07: Exclamation markGHS09: Environmental hazard
Warning
H272,H302,H315,H319,H400
P210,P220,P221,P264,P270,P273,P280,P301+P312,P302+P352,P305+P351+P338,P321,P330,P332+P313,P337+P313,P362,P370+P378,P391,P501
NFPA 704 (fire diamond)
Safety data sheet (SDS)Sigma-Aldrich
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Silver nitrite is aninorganic compound with the formula AgNO2.[2]

Applications

[edit]

Silver nitrite has many applications. Notable examples include:


Production

[edit]

Silver nitrite is produced from the reaction betweensilver nitrate and an alkali nitrite, such assodium nitrite.[3] Silver nitrite is much less soluble in water than silver nitrate, and a solution of silver nitrate will readily precipitate silver nitrite upon addition of sodium nitrite:

AgNO3(aq) + NaNO2(s) → NaNO3(aq) + AgNO2(precipitate)

Alternatively, it can be produced by the reaction betweensilver sulfate andbarium nitrite.

References

[edit]
  1. ^"Silver nitrite".pubchem.ncbi.nlm.nih.gov. Retrieved15 December 2021.
  2. ^American elements
  3. ^abKornblum, N.; Ungnade, H. E. (1958)."1-Nitroöctane (Octane, 1-nitro-)"(PDF).Organic Syntheses.38: 75. Retrieved6 January 2014.
  4. ^Waldman, Steve; Monte, Aaron, Monte; Bracey, Ann & Nichols, David (1996). "One-pot Claisen rearrangement/O-methylation/alkene isomerization in the synthesis of ortho-methoxylated phenylisopropylamines".Tetrahedron Letters.37 (44):7889–7892.doi:10.1016/0040-4039(96)01807-2.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^Nociarova, Jela; Purkait, Anisha; Gyepes, Robert; Hrobarik, Peter (2024)."Silver-Catalyzed Skeletal Editing of Benzothiazol-2(3H)-ones and 2-Halogen-Substituted Benzothiazoles as a Rapid Single-Step Approach to Benzo[1,2,3]Thiadiazoles".Organic Letters.26:619–624.
Silver(0,I)
Silver(I)
Organosilver(I) compounds
Silver(II)
Silver(III)
Silver(I,III)
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