225622
4-Amino-3,5,6-trichloropyridine-2-carboxylic acid
technical grade
Synonym(s):
4-Amino-3,5,6-trichloropicolinic acid, Picloram
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About This Item
grade
technical grade
mp
200 °C (dec.) (lit.)
SMILES string
Nc1c(Cl)c(Cl)nc(C(O)=O)c1Cl
InChI
1S/C6H3Cl3N2O2/c7-1-3(10)2(8)5(9)11-4(1)6(12)13/h(H2,10,11)(H,12,13)
InChI key
NQQVFXUMIDALNH-UHFFFAOYSA-N
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Plant science : an international journal of experimental plant biology, 185-186, 169-175 (2012-02-14)
The cell wall composition of apples callus cultures showed changes in the presence of 5 mg l(-1) of three different plant growth regulators (PGRs), namely picloram, abscisic acid and gibberellic acid. Although the structural functions of cell walls do not
Ecological applications : a publication of the Ecological Society of America, 18(6), 1489-1500 (2008-09-05)
Small-mammal seed predation is an important force structuring native-plant communities that may also influence exotic-plant invasions. In the intermountain West, deer mice (Peromyscus maniculatus) are prominent predators of native-plant seeds, but they avoid consuming seeds of certain widespread invasives like
Molecular plant, 5(3), 619-628 (2012-02-09)
We investigated the diurnal dependence of the hypocotyl-growth responses to shade under sunlight-night cycles in Arabidopsis thaliana. Afternoon shade events promoted hypocotyl growth, while morning shade was ineffective. The lhy-D, elf3, lux, pif4 pif5, toc1, and quadruple della mutants retained
Nature chemical biology, 8(5), 477-485 (2012-04-03)
The plant hormone auxin regulates virtually every aspect of plant growth and development. Auxin acts by binding the F-box protein transport inhibitor response 1 (TIR1) and promotes the degradation of the AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) transcriptional repressors. Here we show that
Journal of hazardous materials, 153(1-2), 718-727 (2007-10-16)
The degradation of the picloram, a widely used herbicide, has been undertaken by the electrochemical advanced oxidation process, namely electro-Fenton in aqueous solution. This process generates catalytically hydroxyl radicals that are strong oxidizing reagents for the oxidation of organic substances.
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