N,N-Dimethylethylamine: Difference between revisions
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{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}} |
{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}} |
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|ImageFile=N,N-Dimethylethylamine.svg |
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|=''N'',''N''- |
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|=Dimethylethylamine |
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| PIN = ''N'',''N''-Dimethylethanamine |
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| OtherNames = Ethyl(dimethyl)amine |
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| UNII = 9N5384XVEM |
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| IUPHAR_ligand = 5523 |
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| CASNo_Ref = {{cascite|correct|??}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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|Section2={{Chembox Properties |
|Section2={{Chembox Properties |
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| C=4|H=11|N=1 |
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| Appearance=Volatile liquid at room temp. |
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| Density= 0.7±0.1 g/cm<sup>3</sup> |
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| MeltingPtC=-140 |
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| BoilingPtC= 36.5 |
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| Solubility= |
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| VaporPressure = 495.4±0.1 mmHg |
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| pKa = 10.16 (for the conjugate acid) (H<sub>2</sub>O)<ref name=toxnet/> |
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|Section3={{Chembox Hazards |
|Section3={{Chembox Hazards |
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| FlashPt= |
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| AutoignitionPt = |
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| Autoignition= |
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'''''N'',''N''-Dimethylethylamine''' ('''DMEA'''), sometimes referred to as dimethylethylamine, is an [[organic compound]] with formula |
'''''N'',''N''-Dimethylethylamine''' ('''DMEA'''), sometimes referred to as dimethylethylamine, is an [[organic compound]] with formula H. It is an chemical that is mainly used in foundries as a catalyst for sand core production.<ref>{{cite web|title=Dimethylethylamine|url=http://www.basf.com/group/corporate/us/en/brand/N_N_DIMETHYLETHYLAMINE|publisher=BASF The Chemical Company|accessdate=4 May 2014}}</ref> Dimethylethylamine is a malodorous, volatile liquid at room temperature that is excreted at greater concentrations with larger dietary intake of [[trimethylamine]].<ref>{{cite web|title=N,N-Dimethylethylamine|url=http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+5712|work=Toxnet|publisher=Hazardous Substance Data Bank|accessdate=4 May 2014|quote=The aim was to study the effect of trimethylamine (TMA) on the metabolism of the industrial catalyst N,N-dimethylethylamine to ascertain whether biological monitoring of industrial exposure to N,N-dimethylethylamine is compromised and excretion of the malodorous N,N-dimethylethylamine in sweat and urine is increased by dietary intake of TMA....Although the increased urinary and hidrotic excretion of N,N-dimethylethylamine may contribute to body odor problems, they were primarily due to TMA excretion, which is much the greater.|-= |-=./..|url=}}</ref> |
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==See also== |
==See also== |
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==References== |
==References== |
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{{TAAR ligands}} |
{{TAAR ligands}} |
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{{DEFAULTSORT:Dimethylethylamine, N,N-}} |
{{DEFAULTSORT:Dimethylethylamine, N,N-}} |
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[[Category:Ethylamines]] |
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[[Category:Foul-smelling chemicals]] |
[[Category:Foul-smelling chemicals]] |
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[[Category:Dimethylamino compounds]] |
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