Terbuthylazine

Terbuthylazine
Names
	IUPAC name N-tert-butyl-6-chloro-N'-ethyl-1,3,5-triazine-2,4-diamine
Identifiers
CAS Number	5915-41-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:30263 ;
ChemSpider	20848 ;
ECHA InfoCard	100.025.125
KEGG	C18810 ;
PubChem CID	22206;
UNII	M095B391J7 ;
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) Key: FZXISNSWEXTPMF-UHFFFAOYSA-N ; 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;
	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). verify (what is ?) Infobox references

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]

Referenced

^ 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. 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. doi:10.1080/03601234.2018.1474556. PMID 29842837.