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About This Item
Empirical Formula (Hill Notation):
C6H3Cl3N2O2
CAS Number:
Molecular Weight:
241.46
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-636-1
Beilstein/REAXYS Number:
479075
MDL number:
InChI key
NQQVFXUMIDALNH-UHFFFAOYSA-N
InChI
1S/C6H3Cl3N2O2/c7-1-3(10)2(8)5(9)11-4(1)6(12)13/h(H2,10,11)(H,12,13)
SMILES string
Nc1c(Cl)c(Cl)nc(C(O)=O)c1Cl
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
mp
200 °C (dec.) (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
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Related Categories
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
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
Storage Class
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
flash_point_f
No data available
flash_point_c
No data available
Regulatory Information
农药列管产品
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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
Alexandre G S Prado et al.
Journal of agricultural and food chemistry, 59(16), 8847-8852 (2011-07-07)
Hexagonal mesoporous silica modified with carboxylic acid (SiAc) has been obtained by reaction between chloroacetic acid and 3-aminopropyltrimethoxysilane, which was immobilized on porous material by a sol-gel process in the presence of an n-dodecylamine template. SiAc was characterized by TG
Lijuan Chen et al.
Analytical biochemistry, 407(2), 172-179 (2010-08-17)
Picloram, a herbicide widely used for broadleaf weed control, is persistent and mobile in soil and water with adverse health and environmental effects. It is important to develop a sensitive method for accurate detection of trace picloram in the environment.
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