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{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}} |
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{{DISPLAYTITLE:''N'',''N''-Dimethylethylamine}} |
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|ImageFile=N,N-Dimethylethylamine.svg |
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| verifiedrevid = 607448118 |
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|IUPACName=''N'',''N''-Dimethylethanamine |
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| Name = ''N'',''N''-Dimethylethylamine |
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|OtherNames=Dimethylethylamine |
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| ImageFile = N,N-Dimethylethylamine.svg |
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|Section1={{Chembox Identifiers |
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| PIN = ''N'',''N''-Dimethylethanamine |
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| CASNo=598-56-1 |
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| OtherNames = Ethyl(dimethyl)amine |
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| ChemSpiderID = 11230 |
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| Section1 = {{Chembox Identifiers |
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| PubChem=11723 |
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| UNII = 9N5384XVEM |
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| SMILES=CCN(C)C |
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| IUPHAR_ligand = 5523 |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo=598-56-1 |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 11230 |
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| PubChem=11723 |
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| SMILES=CCN(C)C |
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|Section2={{Chembox Properties |
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| Section2 = {{Chembox Properties |
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| C=4|H=11|N=1 |
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| C=4 | H=11 | N=1 |
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| Appearance=Volatile liquid at room temp. |
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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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| Density= 0.7±0.1 g/cm<sup>3</sup> |
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| MeltingPtC=-140 |
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| MeltingPtC=-140 |
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| BoilingPtC= 36.5 |
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| BoilingPtC= 36.5 |
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| VaporPressure = 495.4±0.1 mmHg |
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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 |
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| Section3 = {{Chembox Hazards |
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'''''N'',''N''-Dimethylethylamine''' ('''DMEA'''), sometimes referred to as dimethylethylamine, is an ] 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 ].<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 ] of ].<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> |
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'''''N'',''N''-Dimethylethylamine''' ('''DMEA'''), sometimes referred to as dimethylethylamine, is an ] with formula (CH<sub>3</sub>)<sub>2</sub>NC<sub>2</sub>H<sub>5</sub>. It is an industrial chemical that is mainly used in foundries as a catalyst for ]s and ] as well as sand core production.<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title=Amines, Aliphatic|year=2000|last1= Eller|first1=Karsten|last2=Henkes|first2=Erhard|last3=Rossbacher|first3=Roland|last4=Höke|first4=Hartmut|isbn=3527306730}}</ref> <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 ].<ref name=toxnet>{{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.|archive-date=16 September 2018|archive-url=https://web.archive.org/web/20180916144239/https://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+5712|url-status=dead}}</ref> |
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==See also== |
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==See also== |
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==References== |
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==References== |
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{{TAAR ligands}} |
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{{DEFAULTSORT:Dimethylethylamine, N,N-}} |
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