CAS 55335-06-3
:Triclopyr
Description:
Triclopyr is a systemic herbicide primarily used for the control of woody plants and broadleaf weeds. It belongs to the pyridine class of chemicals and functions by mimicking the natural plant hormone auxin, leading to uncontrolled growth and eventual plant death. Triclopyr is particularly effective against invasive species and is often employed in forestry, agriculture, and land management practices. It is available in various formulations, including ester and amine forms, which influence its solubility and application methods. The substance is generally considered to have low toxicity to mammals, but it can be harmful to aquatic organisms, necessitating careful application to minimize environmental impact. Triclopyr is absorbed through foliage and roots, making it effective for both foliar and soil applications. Its persistence in the environment can vary based on factors such as soil type, temperature, and microbial activity, which can influence its degradation rate. Overall, Triclopyr is a valuable tool in integrated pest management strategies, particularly for managing unwanted vegetation.
Formula:C7H4Cl3NO3
InChI:InChI=1S/C7H4Cl3NO3/c8-3-1-4(9)7(11-6(3)10)14-2-5(12)13/h1H,2H2,(H,12,13)
InChI key:InChIKey=REEQLXCGVXDJSQ-UHFFFAOYSA-N
SMILES:O(CC(O)=O)C1=C(Cl)C=C(Cl)C(Cl)=N1
Synonyms:- (3,5,6-Trichloro-2-Pyridinyl)Oxyacetic Acid
- 2-[(3,5,6-Trichloro-2-pyridinyl)oxy]acetic acid
- 2-[(3,5,6-Trichloropyridinyl)oxy]acetic acid
- 3,4,6-Trichloro-2-Pyridinyloxyacetic Acid
- 3,5,6-Tpa
- 3,5,6-Trichloro-2- Pyridyloxyacetic Acid
- 3,5,6-Trichloro-2-pyridinyloxyacetic acid
- 3,5,6-Trichloro-2-pyridinyloxyethanoic acid
- Acetic acid, 2-[(3,5,6-trichloro-2-pyridinyl)oxy]-
- Acetic acid, [(3,5,6-trichloro-2-pyridinyl)oxy]-
- Acetic acid, [(3,5,6-trichloro-2-pyridyl)oxy]-
- Dowco 233
- Garlon
- Garlon 2
- Garlon 250
- Grandstsnd
- Maxim
- Maxim (auxin)
- NSC 190671
- Redeem
- Release
- Remedy
- See more synonyms
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Found 14 products.
Triclopyr
CAS:Formula:C7H4Cl3NO3Purity:>96.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:256.46Triclopyr
CAS:<p>Triclopyr (NSC 190671) is a synthetic growth hormone-like herbicide and fungicide with cytotoxicity and mitochondrial damage induced in rat liver</p>Formula:C7H4Cl3NO3Purity:99.71%Color and Shape:Fluffy Colorless Solid White Or Colourless Fluffy CrystalsMolecular weight:256.47Triclopyr 100 µg/mL in Acetonitrile
CAS:Formula:C7H4Cl3NO3Color and Shape:ColourlessMolecular weight:256.47Pesticide-Mix 95 1000 µg/mL in Ethyl acetate
CAS:Controlled Product- 120-36-5
- 1689-83-4
- 1689-84-5
- 1918-00-9
- 25057-89-0
- 50-31-7
- 55335-06-3
- 93-65-2
- 93-76-5
- 94-74-6
- 94-75-7
- 94-81-5
- 94-82-6
Formula:C7H3Cl3O2Color and Shape:ColourlessMolecular weight:225.46Triclopyr 100 µg/mL in Acetone
CAS:Controlled ProductFormula:C7H4Cl3NO3Color and Shape:Single SolutionMolecular weight:256.47Pesticide-Mix 128 20 µg/mL in Acetonitrile
CAS:Controlled Product- 120-36-5
- 1702-17-6
- 1918-00-9
- 1918-02-1
- 25057-89-0
- 314-40-9
- 55335-06-3
- 69335-91-7
- 69806-34-4
- 882-09-7
- 93-65-2
- 93-72-1
- 93-76-5
- 94-74-6
- 94-75-7
- 94-81-5
- 94-82-6
Formula:C8H5Cl3O3Color and Shape:MixtureMolecular weight:255.48Pesticide Mixture 254 200 µg/mL in Acetonitrile
CAS:- 114311-32-9
- 133-90-4
- 1702-17-6
- 1918-00-9
- 1918-02-1
- 25057-89-0
- 55335-06-3
- 81334-34-1
- 81335-37-7
- 81335-77-5
- 93-65-2
- 94-74-6
- 94-75-7
Formula:C8H6Cl2O3Color and Shape:ColourlessMolecular weight:221.04Triclopyr
CAS:<p>Applications Triclopyr is a selective post-emergence herbicide.<br>References Coupe, R., et al.: Sci. Total Environ., 248, 227 (2000), Lu, C., et al.: Environ. Res., 84, 290 (2000),<br></p>Formula:C7H4Cl3NO3Color and Shape:ColourlessMolecular weight:256.472-[(3,5,6-Trichloro-2-pyridinyl)oxy]acetic acid
CAS:<p>Carbaryl is a broad-spectrum insecticide that has been used to control pests in homes, gardens, and agricultural fields. It can be found in many products for use around the home, including flea collars and ant traps. Carbaryl is absorbed by plants through their leaves and roots and can affect photosynthetic activity. Carbaryl also affects plant metabolism by inhibiting proximal tubule function, which leads to an increase in urea nitrogen and urine production. Carbaryl can be toxic to humans when ingested or inhaled. The toxicity of carbaryl depends on its route of exposure (oral, inhalation, or skin). Carbaryl is metabolized through a number of metabolic reactions that include oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>Formula:C7H4Cl3NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:256.47 g/mol
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