Misplaced Pages

Acetanisole: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 20:38, 30 December 2023 editDMacks (talk | contribs)Edit filter managers, Autopatrolled, Administrators186,558 edits ChemID -> PubChem← Previous edit Revision as of 17:35, 2 January 2024 edit undoMazewaxie (talk | contribs)Extended confirmed users, Pending changes reviewers, Rollbackers113,605 editsm formattingTag: AWBNext edit →
Line 34: Line 34:
}} }}


'''Acetanisole''' is an ] ] with an aroma described as sweet, fruity, nutty, and similar to vanilla. In addition acetanisole can sometimes smell like butter or caramel.<ref name=Aldrich/> Its chemical names are based on considering the structure as either an ] (-]) analog of ]. Other names It can also be seen as a ] analog of ]. '''Acetanisole''' is an ] ] with an aroma described as sweet, fruity, nutty, and similar to vanilla. In addition acetanisole can sometimes smell like butter or caramel.<ref name=Aldrich/> Its chemical names are based on considering the structure as either an ] (]-]) analog of ]. Other names It can also be seen as a ] analog of ].


Acetanisole is found naturally in ], the glandular secretion of the ].<ref name="goodscents"/> Acetanisole is found naturally in ], the glandular secretion of the ].<ref name="goodscents"/>
Line 41: Line 41:
Acetanisole can be prepared ] by ] of anisole with ]: Acetanisole can be prepared ] by ] of anisole with ]:
:] :]

==Application== ==Application==
It is used as a ],<ref> {{webarchive|url=https://web.archive.org/web/20080411182413/http://tobaccodocuments.org/profiles/additives/acetanisole.html|date=April 11, 2008}}</ref> a fragrance,<ref name=goodscents/> and a flavoring in ].<ref>{{CodeFedReg|21|172|515}}</ref> It is used as a ],<ref> {{webarchive|url=https://web.archive.org/web/20080411182413/http://tobaccodocuments.org/profiles/additives/acetanisole.html|date=April 11, 2008}}</ref> a fragrance,<ref name=goodscents/> and a flavoring in ].<ref>{{CodeFedReg|21|172|515}}</ref>

Revision as of 17:35, 2 January 2024

Acetanisole
Names
Preferred IUPAC name 1-(4-Methoxyphenyl)ethan-1-one
Other names 4-Acetylanisole; para-Acetanisole; 4-Methoxyacetophenone; Linarodin; Novatone; Vananote; Castoreum anisole; 4-Methoxyphenyl methyl ketone
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.560 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3
SMILES
  • CC(=O)C1=CC=C(C=C1)OC
Properties
Chemical formula C9H10O2
Molar mass 150.177 g·mol
Appearance White to pale yellow crystals
Density 1.094 g/cm
Melting point 38.2 °C (100.8 °F; 311.3 K)
Boiling point 254 °C (489 °F; 527 K)
Solubility in water 2470 mg/L
Hazards
Flash point 138 °C (280 °F)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Acetanisole is an aromatic chemical compound with an aroma described as sweet, fruity, nutty, and similar to vanilla. In addition acetanisole can sometimes smell like butter or caramel. Its chemical names are based on considering the structure as either an acetyl (methyl-ketone) analog of anisole. Other names It can also be seen as a methyl ether analog of acetophenone.

Acetanisole is found naturally in castoreum, the glandular secretion of the beaver.

Preparation

Acetanisole can be prepared synthetically by Friedel-Crafts acylation of anisole with acetyl chloride:

Application

It is used as a cigarette additive, a fragrance, and a flavoring in food.

References

  1. ^ Para-Acetanisole, The Good Scents Company
  2. ^ 4'-Methoxyacetophenone from PubChem
  3. ^ Acetanisole at Sigma-Aldrich
  4. Tobacco Documents | Profiles | Additives | Acetanisole Archived April 11, 2008, at the Wayback Machine
  5. 21 CFR 172.515
Categories: