| Revision as of 16:48, 12 May 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 03:47, 2 January 2025 edit undoDiscospinster (talk | contribs)Administrators465,015 editsm Reverted edits by 2405:201:A431:9836:D84E:93FC:4AE5:8759 (talk) (HG) (3.4.12)Tags: Huggle Rollback |
| (36 intermediate revisions by 29 users not shown) |
| Line 1: |
Line 1: |
|
{{Orphan|date=February 2009}} |
|
|
|
|
|
{{chembox |
|
{{chembox |
|
|
| Verifiedfields = changed |
| ⚫ |
| verifiedrevid = 398941140 |
|
|
|
| Watchedfields = changed |
| ⚫ |
|Reference=<ref>'']'', 11th Edition, '''7880'''</ref> |
|
|
⚫ |
| verifiedrevid = 428780603 |
| ⚫ |
|ImageFile=Propyl propanoate.png |
|
|
⚫ |
| Reference =<ref>'']'', 11th Edition, '''7880'''</ref> |
| ⚫ |
|ImageSize=200px |
|
|
|IUPACName=Propyl propanoate |
|
| ImageFile =Propyl propanoate Structural Formula V1.svg |
|
⚫ |
| ImageSize = |
| ⚫ |
|OtherNames=Propyl propionate |
|
|
⚫ |
| PIN = Propyl propanoate |
|
⚫ |
| OtherNames = Propyl propionate |
|
|Section1={{Chembox Identifiers |
|
|Section1={{Chembox Identifiers |
|
|
| CASNo_Ref = {{cascite|correct|??}} |
|
| CASNo=106-36-5 |
|
| CASNo = 106-36-5 |
| ⚫ |
| PubChem=7803 |
|
|
|
| UNII_Ref = {{fdacite|changed|FDA}} |
| ⚫ |
| SMILES=CCCOC(=O)CC |
|
|
|
| UNII = G09TRV00GK |
|
⚫ |
| PubChem = 7803 |
|
|
| ChEBI_Ref = {{ebicite|changed|EBI}} |
|
|
| ChEBI = 89828 |
|
⚫ |
| SMILES = CCCOC(=O)CC |
|
|
| EINECS = 203-389-7 |
|
|
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
|
|
| ChemSpiderID = 7515 |
|
|
| InChI = 1/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3 |
|
|
| InChIKey = MCSINKKTEDDPNK-UHFFFAOYAX |
|
|
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChI = 1S/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3 |
|
|
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChIKey = MCSINKKTEDDPNK-UHFFFAOYSA-N |
|
}} |
|
}} |
|
|Section2={{Chembox Properties |
|
|Section2={{Chembox Properties |
|
| C = 6 | H = 12 | O = 2 |
|
| C=6 | H=12 | O=2 |
|
| Appearance= |
|
| Appearance = |
|
| Density= 0.833 g/cm<sup>3</sup> at 20 °C |
|
| Density = 0.833{{nbsp}}g/cm<sup>3</sup> at 20{{nbsp}}°C |
|
| MeltingPtC=-76 |
|
| MeltingPtC = −76 |
|
|
| BoilingPtC = 122–124 |
|
| BoilingPt=122-124 °C |
|
|
|
| BoilingPt_notes = |
|
| Solubility=1 part per 200 |
|
| Solubility = 1 part per 200 |
|
}} |
|
}} |
|
|Section3={{Chembox Hazards |
|
|Section3={{Chembox Hazards |
|
| ExternalMSDS = |
|
| ExternalSDS = |
|
| FlashPt= |
|
| FlashPt = |
|
|
| AutoignitionPt = |
|
| Autoignition= |
|
|
}} |
|
}} |
|
}} |
|
}} |
|
|
|
|
|
'''Propyl propanoate''' is an ] formed from the esterification of ] and ]. Like most esters, propyl propanoate has a distinctly fruity odor which may be described as a chemically tinged ]. It may be used as a ].<ref></ref> |
|
'''Propyl propanoate''' (also known as '''propyl propionate''' and '''''n''-propyl propionate''') is the ] with the ] ]<sub>6</sub>]<sub>12</sub>]<sub>2</sub>. It is the ] of ] and ]. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged ] or ]. It is used in perfumery and as a ].<ref></ref><ref>{{cite encyclopedia|author= |
|
|
Anthony J. Papa|title=Propanols|encyclopedia=Ullmann’s Encyclopedia of Industrial Chemistry|year=2011|publisher=Wiley-VCH|place=Weinheim|doi=10.1002/14356007.a22_173.pub2}}</ref> The refractive index at 20 °C is 1.393. |
|
|
|
|
|
Because propyl propanoate is a low-odor, moderately volatile ester solvent that is not a hazardous air pollutant (HAP), with good solvent activity and versatility,<ref>{{cite web | url = https://www.pcimag.com/articles/85514-replacing-hap-solvents-xylene-and-toluene-p-nuts-bolts-april-2006? | date = April 1, 2006 | title = Replacing HAP Solvents: Xylene and Toluene | publisher = Paint & Coatings Industry }}</ref> it is considered a safer substitute for ]. |
|
|
|
|
|
==References== |
|
==References== |
|
{{reflist}} |
|
{{reflist}} |
|
|
{{Esters}} |
|
|
|
|
|
] |
|
] |
|
|
] |
|
|
|
|
|
|
|
|
|
{{ester-stub}} |
|
{{ester-stub}} |
|
|
|
|
] |
|
|
] |
|
|
] |
|
|
] |
|