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Wikipedia

Terbuthylazine

Terbuthylazine is a selective herbicide. Chemically, it is a chlorotriazine; compared with atrazine and simazine, it has a tert-butyl group in place of the isopropyl and ethyl groups, respectively.[1][2]

Terbuthylazine
Names
Preferred IUPAC name
N2-tert-Butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine
Identifiers
  • 5915-41-3 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:30263 Y
ChemSpider
  • 20848 Y
ECHA InfoCard 100.025.125
KEGG
  • C18810 Y
  • 22206
UNII
  • M095B391J7 Y
  • DTXSID4027608
  • InChI=1S/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) Y
    Key: FZXISNSWEXTPMF-UHFFFAOYSA-N Y
  • 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)
    Key: FZXISNSWEXTPMF-UHFFFAOYAN
  • Clc1nc(nc(n1)NC(C)(C)C)NCC
Properties
C9H16ClN5
Molar mass 229.710 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

Referenced edit

  1. ^ Dousset, S.; Mouvet, C.; Schiavon, M. (1994). "Sorption of terbuthylazine and atrazine in relation to the physico-chemical properties of three soils". Chemosphere. 28 (3): 467–476. Bibcode:1994Chmsp..28..467D. doi:10.1016/0045-6535(94)90291-7.
  2. ^ Carretta, L.; Cardinali, A.; Marotta, E.; Zanin, G.; Masin, R. (2018). "Dissipation of terbuthylazine, metolachlor, and mesotrione in soils with contrasting texture". J Environ Sci Health B. 53 (10): 661–668. Bibcode:2018JESHB..53..661C. doi:10.1080/03601234.2018.1474556. PMID 29842837. S2CID 44163175.

terbuthylazine, this, article, needs, additional, citations, verification, please, help, improve, this, article, adding, citations, reliable, sources, unsourced, material, challenged, removed, find, sources, news, newspapers, books, scholar, jstor, january, 20. This article needs additional citations for verification Please help improve this article by adding citations to reliable sources Unsourced material may be challenged and removed Find sources Terbuthylazine news newspapers books scholar JSTOR January 2021 Learn how and when to remove this message Terbuthylazine is a selective herbicide Chemically it is a chlorotriazine compared with atrazine and simazine it has a tert butyl group in place of the isopropyl and ethyl groups respectively 1 2 Terbuthylazine Names Preferred IUPAC name N2 tert Butyl 6 chloro N4 ethyl 1 3 5 triazine 2 4 diamine Identifiers CAS Number 5915 41 3 Y 3D model JSmol Interactive image ChEBI CHEBI 30263 Y ChemSpider 20848 Y ECHA InfoCard 100 025 125 KEGG C18810 Y PubChem CID 22206 UNII M095B391J7 Y CompTox Dashboard EPA DTXSID4027608 InChI InChI 1S 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 YKey FZXISNSWEXTPMF UHFFFAOYSA N YInChI 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 Key FZXISNSWEXTPMF UHFFFAOYAN SMILES Clc1nc nc n1 NC C C C NCC Properties Chemical formula C9H16ClN5 Molar mass 229 710 g mol Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox referencesReferenced edit Dousset S Mouvet C Schiavon M 1994 Sorption of terbuthylazine and atrazine in relation to the physico chemical properties of three soils Chemosphere 28 3 467 476 Bibcode 1994Chmsp 28 467D doi 10 1016 0045 6535 94 90291 7 Carretta L Cardinali A Marotta E Zanin G Masin R 2018 Dissipation of terbuthylazine metolachlor and mesotrione in soils with contrasting texture J Environ Sci Health B 53 10 661 668 Bibcode 2018JESHB 53 661C doi 10 1080 03601234 2018 1474556 PMID 29842837 S2CID 44163175 Retrieved from https en wikipedia org w index php title Terbuthylazine amp oldid 1206054060, wikipedia, wiki, book, books, library,

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