| Revision as of 02:51, 30 May 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (changes to verified fields - added verified revid - updated 'UNII_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:WikiProject_Chemicals|← Previous edit |
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{{more citations needed|date=January 2021}} |
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{{chembox |
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{{chembox |
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| verifiedrevid = 470602280 |
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| ImageFile = Terbuthylazine.png |
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| verifiedrevid = 402681753 |
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| ImageAlt = Skeletal formula of terbuthylazine |
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|ImageFile=Terbuthylazine.png |
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| ImageFile1 = Terbuthylazine-3D-spacefill.png |
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| ImageAlt1 = Space-filling model of the terbuthylazine molecule |
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|IUPACName=N-tert-butyl-6-chloro-N'-ethyl-1,3,5-triazine-2,4-diamine |
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| PIN=''N''<sup>2</sup>-''tert''-Butyl-6-chloro-''N''<sup>4</sup>-ethyl-1,3,5-triazine-2,4-diamine |
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|OtherNames= |
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|Section1={{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 20848 |
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| ChemSpiderID = 20848 |
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| InChI = 1/C9H16ClN5/c1-5-11-7-12-6(10)13-8(14-7)15-9(2,3)4/h5H2,1-4H3,(H2,11,12,13,14,15) |
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| InChI = 1/C9H16ClN5/c1-5-11-7-12-6(10)13-8(14-7)15-9(2,3)4/h5H2,1-4H3,(H2,11,12,13,14,15) |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo=5915-41-3 |
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| CASNo=5915-41-3 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| PubChem=22206 |
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| UNII = M095B391J7 |
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| KEGG_Ref = {{keggcite|changed|kegg}} |
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| PubChem=22206 |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = C18810 |
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| KEGG = C18810 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| SMILES = Clc1nc(nc(n1)NC(C)(C)C)NCC |
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| ChEBI = 30263 |
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| SMILES = Clc1nc(nc(n1)NC(C)(C)C)NCC |
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|Section2={{Chembox Properties |
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|Section2={{Chembox Properties |
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| Formula=C<sub>9</sub>H<sub>16</sub>ClN<sub>5</sub> |
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| Formula=C<sub>9</sub>H<sub>16</sub>ClN<sub>5</sub> |
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| MolarMass=229.710 g/mol |
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| MolarMass=229.710 g/mol |
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|Section3={{Chembox Hazards |
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|Section3={{Chembox Hazards |
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'''Terbuthylazine''' is a selective ]. Chemically, it is a halogenated ]; compared with ] (1958 inv., ] lab) and ], it has a ] group <chem display="inline">-</chem> in place of the ] <chem display="inline">-</chem> and ] group, respectively.<ref>{{cite journal|title=Sorption of terbuthylazine and atrazine in relation to the physico-chemical properties of three soils|journal=]|volume=28|issue=3|pages=467–476|doi=10.1016/0045-6535(94)90291-7|year=1994|last1=Dousset|first1=S.|last2=Mouvet|first2=C.|last3=Schiavon|first3=M.|bibcode=1994Chmsp..28..467D }}</ref><ref>{{cite journal|title=Dissipation of terbuthylazine, metolachlor, and mesotrione in soils with contrasting texture|journal=]|volume=53|issue=10|pages=661–668|doi=10.1080/03601234.2018.1474556|year=2018|last1=Carretta|first1=L.|last2=Cardinali|first2=A.|last3=Marotta|first3=E.|last4=Zanin|first4=G.|last5=Masin|first5=R.|pmid=29842837|bibcode=2018JESHB..53..661C |s2cid=44163175 }}</ref> The sim-azine molecule with 2 ethyl groups is symmetric and flat (excepting its equal <chem display="inline">NH-C2H5</chem>ends). The threefold substituted triazines have ] of the free (non-bonding, <math display="inline">\pi</math>-) electron pairs, resulting in equivalent ] structures. |
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'''Terbuthylazine''' is a selective ]. Chemically, it is a ]; compared with ] and ], it has a ] group in place of the ] and ] groups, respectively. |
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<Simazine remains active in the soil for 2 to 7 months or longer after application. Atrazine remains in soil for a matter of months (although in some soils can persist to at least 4 years)<ref>Atrazine: Chemical Summary. Toxicity and Exposure Assessment for Children's Health (PDF) (Report). U.S. ]. 2007-04-24. Archived from the original (PDF) on 2012-03-16.</ref> and can migrate from soil to ].> |
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==References== |
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==References== |
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{{reflist}} |
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{{German|Terbuthylazine|09:48, 15 June 2008 (UTC)}} |
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{{Herbicides}} |
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