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
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)
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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
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
J F Fairchild et al.
Archives of environmental contamination and toxicology, 56(4), 761-769 (2008-09-12)
We conducted acute and chronic toxicity studies of the effects of picloram acid on the threatened bull trout (Salvelinus confluentus) and the standard coldwater surrogate rainbow trout (Oncorhynchus mykiss). Juvenile fish were chronically exposed for 30 days in a proportional
Romina Sellaro et al.
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
Ting Li et al.
Huan jing ke xue= Huanjing kexue, 29(6), 1660-1665 (2008-09-04)
A "sandwich-type" immunosensor for the determination of picloram in water environment was developed based on the immunoliposomes prepared by crosslinking rabbit antibody against picloram (anti-picloram) and potassium ferrocyanide-encapsulated liposomes with glutaraldehyde. The working conditions including modification components on the electrode
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