To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Aluminium monoacetate

From Wikipedia, the free encyclopedia

Aluminium monoacetate
Names
IUPAC name
Aluminium monoacetate
Other names
Basic aluminium monoacetate Dihydroxyaluminium acetate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C2H4O2.Al.2H2O/c1-2(3)4;;;/h1H3,(H,3,4);;2*1H2/q;+3;;/p-3
    Key: KLMDYFUUSKOJAX-UHFFFAOYSA-K
  • CC(=O)[O-].[OH-].[OH-].[Al+3]
Properties
(HO)2AlCH3CO2 or C2H5AlO4
Molar mass 120.04 g/mol
Appearance White powder
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Aluminium monoacetate, also known as dibasic aluminium acetate, and formally named dihydroxy aluminium acetate, is a salt of aluminium with acetic acid. It has the formula Al(OH)2(CH3COO), with aluminium in an oxidation state of +3, and appears under standard conditions as a white solid powder.[1]

YouTube Encyclopedic

  • 1/1
    Views:
    2 091
  • This reaction looks like magic #shorts #chemistry #experiment #science

Transcription

Chemistry

Aluminium monoacetate is prepared from the reaction between Al(OH)3 and dilute aqueous acetic acid.[1] It is also formed from the successive hydrolysis of aluminium triacetate.[2][3]

Al(CH3COO)3 + H2O → Al(OH)(CH3COO)2 + CH3COOH
Al(OH)(CH3COO)2 + H2O → Al(OH)2(CH3COO) + CH3COOH

Uses

Aluminium monoacetate is a dermatological agent used as an antiseptic and astringent.[4] It is used as an antiseptic to reduce the possibility of infection in minor wounds, cuts, and burns. Specifically, it treats itching, stinging of the infected skin, inflammation, and it promotes healing. It also can be used as a topical astringent to help shrink the body's tissues when applied to the skin as it acts as a protective layer on irritated and inflamed skin.

References

  1. ^ a b Wade K, Banister AJ, Bailar JC, Emeléus HJ, Nyholm R, eds. (1973). The Chemistry of Aluminium, Gallium, Indium and Thallium : Comprehensive Inorganic Chemistry. Saint Louis: Elsevier Science. p. 1047. ISBN 978-1-4831-5322-3. OCLC 953379198.
  2. ^ Daintith J, ed. (2008). "Aluminium ethanoate (aluminium acetate)". A Dictionary of Chemistry (6th ed.). Oxford University Press. ISBN 9780199204632.
  3. ^ "CharChem. Dihydroxyaluminum Acetate". easychem.org. Retrieved 2020-07-19.
  4. ^ Triggle DJ, Ganellin CR (1997). Dictionary of Pharmacological Agents. Cambridge: Chapman & Hall. pp. 595, 600. ISBN 0412466309.
This page was last edited on 21 March 2024, at 19:46
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.