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Merck
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36774

Supelco

Picloram

PESTANAL®, analytical standard

Sinónimos:

4-Amino-3,5,6-trichloro-pyridine-2-carboxylic acid

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About This Item

Fórmula empírica (notación de Hill):
C6H3Cl3N2O2
Número de CAS:
1918-02-1
Peso molecular:
241.46
Beilstein:
479075
Número CE:
217-636-1
Número MDL:
MFCD00012101
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329755506
NACRES:
NA.24

grado

analytical standard

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

mp

200 °C (dec.) (lit.)

aplicaciones

agriculture
environmental

formato

neat

cadena SMILES

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)

Clave InChI

NQQVFXUMIDALNH-UHFFFAOYSA-N

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Aplicación


  • 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).


Información legal

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Frases de peligro

H412

Consejos de prudencia

P273 - P501

Clasificaciones de peligro

Aquatic Chronic 3

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
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
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
Yingying Tian et al.
Journal of AOAC International, 95(2), 554-559 (2012-06-02)
A sensitive and effective method for the simultaneous quantitative determination of aminopyralid, clopyralid, and picloram in vegetables (eggplant, cucumber, and tomato) and fruits (apple and grape) was developed and validated using ultra-performance LC coupled with MS/MS. The three herbicides were
James F Fairchild et al.
Environmental toxicology and chemistry, 27(3), 623-630 (2007-11-03)
We conducted 96-h static acute toxicity studies to evaluate the relative sensitivity of juveniles of the threatened bull trout (Salvelinus confluentus) and the standard cold-water surrogate rainbow trout (Onchorhyncus mykiss) to three rangeland herbicides commonly used for controlling invasive weeds
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