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Potassium propanoate: Difference between revisions

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Revision as of 17:06, 28 June 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit Latest revision as of 15:41, 11 September 2024 edit undoCitation bot (talk | contribs)Bots5,424,103 edits Added date. | Use this bot. Report bugs. | Suggested by Abductive | Category:E-number additives | #UCB_Category 126/313 
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{{Chembox {{Chembox
| Verifiedfields = changed
| verifiedrevid = 435838956
| Watchedfields = changed
| OtherNames = Potassium propionate; E283
| verifiedrevid = 436702720
| ImageFile = Potassium propionate.svg
| Name =
| ImageSizeL1 = 150px
| ImageFile = Potassium propionate.svg
| Section1 = {{Chembox Identifiers
| ImageFile1 = potassium-propionate-3D-vdW.png
| PIN = Potassium propanoate
| OtherNames = Potassium propionate; E283
| Section1 = {{Chembox Identifiers
| CASNo = 327-62-8 | CASNo = 327-62-8
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo_Ref = {{cascite|correct|??}}
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem = 23663619
| UNII = 7H1F04CKTX
}}
| PubChem = 23663619
| Section2 = {{Chembox Properties
| EINECS = 206-323-5
| Formula = C<sub>3</sub>H<sub>5</sub>KO<sub>2</sub>
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 64232
| InChI = 1/C3H6O2.K/c1-2-3(4)5;/h2H2,1H3,(H,4,5);/q;+1/p-1
| InChIKey = BWILYWWHXDGKQA-REWHXWOFAC
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C3H6O2.K/c1-2-3(4)5;/h2H2,1H3,(H,4,5);/q;+1/p-1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = BWILYWWHXDGKQA-UHFFFAOYSA-M
| SMILES = CCC(=O).
}}
| Section2 = {{Chembox Properties
| Formula = C<sub>3</sub>H<sub>5</sub>KO<sub>2</sub>
| MolarMass = 112.1689 g/mol
| MeltingPt = >300 °C<ref name=Cadogan/> | MeltingPt = >300 °C<ref name=Cadogan/>
| Appearance = Colorless crystalline platelets<ref name=Cadogan>J. I. G. Cadogan, J. Buckingham, F. MacDonald: ''Dictionary of Organic Compounds: First Supplement.'' CRC Press, 1996, ISBN 978-0-412-54110-0</ref> | Appearance = Colorless crystalline platelets<ref name=Cadogan>J. I. G. Cadogan, J. Buckingham, F. MacDonald: ''Dictionary of Organic Compounds: First Supplement.'' CRC Press, 1996, {{ISBN|978-0-412-54110-0}}</ref>
| Solubility = soluble<ref name=Cadogan/> | Solubility = soluble<ref name=Cadogan/>
| SolubleOther = soluble<ref name=Cadogan/> | SolubleOther = soluble<ref name=Cadogan/>
| Solvent = ] | Solvent = ]
}} }}
| Section3 =
| Section4 =
| Section5 =
| Section6 =
}} }}


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==Use== ==Use==
It is used as a ] and is represented by the food labeling ] E283 in Europe<ref>UK Food Standards Agency: {{cite web |url=http://www.food.gov.uk/safereating/chemsafe/additivesbranch/enumberlist |title=Current EU approved additives and their E Numbers |accessdate=2011-10-27}}</ref> and by the ] 283 in Australia and New Zealand.<ref>Australia New Zealand Food Standards Code{{cite web |url=http://www.comlaw.gov.au/Details/F2011C00827 |title=Standard 1.2.4 - Labelling of ingredients |date=8 September 2011 |accessdate=2011-10-27}}</ref>
It is used as a ] and is represented by the food labeling ] E283 in Europe.


== References == == References ==
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