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36774

Supelco

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
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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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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

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

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Unique recombinant human ribonuclease and inhibition of Kaposi's sarcoma cell growth
Newton D L and Rybak S M
Journal of the National Cancer Institute, 90(23), 1787-1791 (1998)
Reducing inositol lipid hydrolysis, Ins (1, 4, 5) P3 receptor availability, or Ca2+ gradients lengthens the duration of the cell cycle in Xenopus laevis blastomeres.
Han J K, et al.
The Journal of Cell Biology, 116(1), 147-156 (1992)
The superovulation of synchronous adult rats using follicle-stimulating hormone delivered by continuous infusion
Scott H G and Armstrong D T
Biology of Reproduction, 44(5), 851-856 (1991)
Umit A Kayisli et al.
Journal of immunology (Baltimore, Md. : 1950), 171(5), 2305-2313 (2003-08-21)
The first known hormonal signal of the conceptus during implantation is human chorionic gonadotropin (hCG). Interestingly, increased apoptosis in human endometrium coincides with the implantation window. Factors from the fetal or placental origin as well as maternal hormonal factors are

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