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N,N-Dimethylethylamine: Difference between revisions

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{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}}
{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}}
{{chembox
{{chembox
| Watchedfields = changed
|ImageFile=N,N-Dimethylethylamine.svg
| verifiedrevid = 607448118
|ImageSize=
|IUPACName=''N'',''N''-Dimethylethanamine
|=''N'',''N''-
|OtherNames=Dimethylethylamine
|=Dimethylethylamine
|ImageSize=
|Section1={{Chembox Identifiers
| PIN = ''N'',''N''-Dimethylethanamine
| CASNo=598-56-1
| OtherNames = Ethyl(dimethyl)amine
| ChemSpiderID = 11230
|Section1={{Chembox Identifiers
| PubChem=11723
| UNII = 9N5384XVEM
| SMILES=CCN(C)C
| IUPHAR_ligand = 5523
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=598-56-1
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 11230
| PubChem=11723
| SMILES=CCN(C)C
}}
}}
|Section2={{Chembox Properties
|Section2={{Chembox Properties
| C=4|H=11|N=1
| C=4|H=11|N=1
| Appearance=Volatile liquid at room temp.
| Appearance=Volatile liquid at room temp.
| Density= 0.7±0.1 g/cm<sup>3</sup>
| Density= 0.7±0.1 g/cm<sup>3</sup>
| MeltingPtC=-140
| MeltingPtC=-140
| BoilingPtC= 36.5
| BoilingPtC= 36.5
| Solubility=
| Solubility=
| VaporPressure = 495.4±0.1 mmHg
| VaporPressure = 495.4±0.1 mmHg
| pKa = 10.16 (for the conjugate acid) (H<sub>2</sub>O)<ref name=toxnet/>
}}
}}
|Section3={{Chembox Hazards
|Section3={{Chembox Hazards
| MainHazards=
| MainHazards=
| FlashPt=
| FlashPt=
| AutoignitionPt =
| Autoignition=
}}
}}
| Section4 =
| Section5 =
| Section6 =
}}
}}


'''''N'',''N''-Dimethylethylamine''' ('''DMEA'''), sometimes referred to as dimethylethylamine, is an [[organic compound]] with formula {{chemical formula|C|4|H|11|N}}. It is an industrual 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.}}</ref> It has recently been identified as an [[agonist]] of [[TAAR5|human trace amine-associated receptor 5]].<ref name="pmid23393561">{{cite journal |author=Wallrabenstein I, Kuklan J, Weber L, Zborala S, Werner M, Altmüller J, Becker C, Schmidt A, Hatt H, Hummel T, Gisselmann G |title=Human trace amine-associated receptor TAAR5 can be activated by trimethylamine |journal=PLoS ONE |volume=8 |issue=2 |pages=e54950 |year=2013 |pmid=23393561 |pmc=3564852 |doi=10.1371/journal.pone.0054950 |url=}}</ref>
'''''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>


==See also==
==See also==
[[Odorant]]
{| width=60%
[[Olfactory receptor]]
|{{bull}}[[Odorant]]
[[Trace amine]]
|{{bull}}[[Olfactory receptor]]
[[Trace amine-associated receptor]]
|-
|{{bull}}[[Trace amine]]
|{{bull}}[[Trace amine-associated receptor]]
|}


==References==
==References==
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{{TAAR ligands}}
{{TAAR ligands}}


{{DEFAULTSORT:Dimethylethylamine, N,N-}}
{{DEFAULTSORT:Dimethylethylamine, N,N-}}
[[Category:Ethylamines]]
[[Category:Foul-smelling chemicals]]
[[Category:Foul-smelling chemicals]]
[[Category:Dimethylamino compounds]]