From Wikipedia, the free encyclopedia
Terbuthylazine
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Names
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Preferred IUPAC name
N2-tert-Butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine
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Identifiers
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ChEBI
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ChemSpider
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ECHA InfoCard
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100.025.125
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KEGG
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UNII
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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
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Clc1nc(nc(n1)NC(C)(C)C)NCC
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Properties
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C9H16ClN5
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Molar mass
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229.710 g/mol
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Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Terbuthylazine is a selective
herbicide. Chemically, it is a halogenated
triazine; compared with
atrazine and
simazine, it has a
tert-butyl group in place of the
isopropyl and
ethyl groups, respectively.
[1]
[2]
Referenced
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^ 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.
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^ 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.