2-[(3,5,6-Trichloro-2-pyridinyl)oxy]acetic acid

CAS: 55335-06-3

Ref. 3D-FT28420

Product Information

• Name: 2-[(3,5,6-Trichloro-2-pyridinyl)oxy]acetic acid
• Synonyms: Triclopyr[(3,5,6-tTichloro-2-pyridyl)oxy]acetic acid3,5,6-TPA, (3,5,6-Trichloro-2-Pyridinyl)Oxyacetic 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, [(3,5,6-Trichloropyridin-2-Yl)Oxy]Acetic Acid

Description

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.

• Brand: Biosynth

Chemical properties

• Molecular weight: 256.47 g/mol
• Formula: C₇H₄Cl₃NO₃
• Purity: Min. 95%
• Color/Form: Powder
• 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=C(O)COc1nc(Cl)c(Cl)cc1Cl