36774
Picloram
PESTANAL®, analytical standard
Synonym(s):
4-Amino-3,5,6-trichloropyridine-2-carboxylic acid, 4-Amino-3,5,6-trichloropicolinic acid, Picloram
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About This Item
Empirical Formula (Hill Notation):
C6H3Cl3N2O2
CAS Number:
Molecular Weight:
241.46
Beilstein:
479075
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
mp
200 °C (dec.) (lit.)
application(s)
agriculture
environmental
format
neat
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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Application
- Herbicide Research: Picloram is explored for its synthesis, bioactivity, and mechanism of action as a herbicide in a novel compound class, showing its efficacy and potential applications in agriculture (Liu et al., 2024).
- Environmental Impact Studies: Research focuses on long-term conservation efforts using Picloram, demonstrating its effectiveness in ex situ plant conservation and understanding its broader environmental impacts (Kocot et al., 2024).
- Molecular Biology: Studies on the fluorescence sensor array for herbicides including Picloram highlight advancements in analytical chemistry, providing a robust method for qualitative and quantitative herbicide analysis (Zhang et al., 2024).
- Pharmacological Properties: The development and validation of methods for analyzing formulations containing Picloram showcase its stable nature and relevance in ensuring the safety and effectiveness of herbicidal products (Marczewska et al., 2024).
- Plant Growth Regulator Studies: Picloram′s role in the synthesis and herbicidal activity of novel compounds supports ongoing research into its use as a plant growth regulator, enhancing our understanding of its molecular effects on plant biology (Liu et al., 2024).
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Customers Also Viewed
Jose L Marco-Brown et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 54(4), 281-289 (2019-02-14)
The picloram (PCM) adsorption on nontronite, illite and kaolinite was studied at pH 3, 5 and 7. The adsorption isotherms had well-fitted to Langmuir and Freundlich models equations. The interactions of PCM with the clay mineral surfaces exhibited an anionic
Solmaz Khosravi et al.
Pakistan journal of biological sciences : PJBS, 10(15), 2517-2521 (2007-08-01)
Experiments were carried out to investigate the effects of various concentrations of Picloram (0, 1, 2, 3, 6 and 9 mg L(-1)), TDZ (0, 0.5, 1, 1.5 and 2 mg L(-1)), NAA (1.5 mg L(-1)) in combination with TDZ (0.08
D A Steinmacher et al.
Annals of botany, 108(8), 1463-1475 (2011-03-01)
Secondary somatic embryogenesis has been postulated to occur during induction of peach palm somatic embryogenesis. In the present study this morphogenetic pathway is described and a protocol for the establishment of cycling cultures using a temporary immersion system (TIS) is
Paula Alayón-Luaces et al.
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
Dean E Pearson et al.
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
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