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7761-88-8 - Silver nitrate, ACS, 99.9+% (metals basis) - 11414 - Alfa Aesar

11414 Silver nitrate, ACS, 99.9+% (metals basis)

Numéro de CAS
7761-88-8
Synonymes

Conditionnement Prix ($) Quantité Disponibilité
5g 25,00
25g 65,20
100g 235,00
500g 1054,00
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Silver nitrate, ACS, 99.9+% (metals basis)

MDL
MFCD00003414
EINECS
231-853-9

Propriétés chimiques

Formule
AgNO3
Poids moleculaire
169.87
Forme
Crystalline
Point de fusion
212°
Densité
4.352
Sensibilité
Light Sensitive
Solubilité
Freely soluble in water, alcohol and aqueous ammonia. Slightly soluble in ether.

Spécifications des grades

Maximum level of impurities: Clarity of solution P.T., Cl 5ppm, Free acid P.T., Substances not precipitated by hydrochloric acid 0.01%, SO4 0.002%, Cu 2ppm, Fe 2ppm, Pb 0.001%

Applications

Silver nitrate is employed in Silver plating, photography, manufacturing of other silver compounds, mirrors, coloring porcelain, and staining in histology. It finds use as a stain in scanning electron microscopy, and a key ingredient in several silver-based antiseptic and antibacterial pharmaceutical compositions. Silver(I) nitrate is used to separate mixtures of alkenes by selective absorption, and for deprotection and oxidation reactions in organic synthesis. It is widely used as an analytical reagent owing to its immediate reaction with halide ions forming insoluble precipitate of silver(I) halides.

Notes

Sensitive to light; hence store in light resistant containers. Corrosive solid. Relatively more stable to light than other salts. Color changes to grey or greyish black on exposure to light or air in the presence of organic matter.

Références bibliographiques

Forms complexes with alkenes, used in the separation of mixtures; see, e.g.: Org. Synth. Coll., 5, 315 (1973).

Promotes the reactivity of NCS in the cleavage of 2-acylated 1,3-dithianes: Synthesis, 17 (1969), and of NBS in the 1-bromination of terminal alkynes: Angew. Chem. Int. Ed., 23, 727 (1984).

In combination with Br2 or I2 in refluxing methanol, brings about the rearrangement of acetophenones to methyl arylacetates, a reaction previously induced by thallium(III) nitrate: J. Chem. Soc., Perkin 1, 235 (1982):

The Hunsdiecker reaction of Ag salts of carboxylic acids with Br2 provides alkyl bromides with one less carbon atom which is lost as CO2; see, e.g.: Org. Synth. Coll., 3, 578 (1955). Reviews: Chem. Rev., 56, 219 (1956); Org. React., 9, 332 (1957). Compare also Mercury(II)­ oxide, A16157.

For the alkylation of substrates by radicals derived from decarboxylation of acids, see Trimethyl­acetic acid, A10776.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H272-H290-H314

May intensify fire; oxidizer. May be corrosive to metals. Causes severe skin burns and eye damage.

Mentions de prudence: P221-P210v-P303+P361+P353-P305+P351+P338-P405-P501a

Take any precaution to avoid mixing with combustibles. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,8518
Classe de danger
5.1
Groupe d'emballage
I
Code tarifaire harmonisé
2843.21
TSCA
Yes
RTECS
VW4725000

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