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  2. 2,4,5-Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,5-Trichlorophenol

    2,4,5-Trichlorophenol (TCP) is an organochloride with the molecular formula C 6 H 3 Cl 3 O.It has been used as a fungicide and herbicide. [2] Precursor chemical used in the production of 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T) and hexachlorophene involves the intermediate production of 2,4,5-trichlorophenol (TCP) and the formation of 2,3,7,8-Tetrachlorodibenzodioxin (TCDD, commonly ...

  3. 2,4,5-Trichlorophenoxyacetic acid - Wikipedia

    en.wikipedia.org/wiki/2,4,5-Trichlorophenoxy...

    2,4,5-Trichlorophenoxyacetic acid (also known as 2,4,5-T), a synthetic auxin, is a chlorophenoxy acetic acid herbicide used to defoliate broad-leafed plants. It was developed in the late 1940s, synthesized by reaction of 2,4,5-Trichlorophenol and chloroacetic acid. It was widely used in the agricultural industry until being phased out, starting ...

  4. 2,4,6-Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trichlorophenol

    2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor.

  5. Chlorpyrifos - Wikipedia

    en.wikipedia.org/wiki/Chlorpyrifos

    The industrial synthesis of chlorpyrifos (3) is made by reacting 3,5,6-trichloro-2-pyridinol (TCPy) (1) with O,O-diethyl phosphorochloridothioate (2): [20] Industrial synthesis of chlorpyrifos Uses

  6. Toxicity class - Wikipedia

    en.wikipedia.org/wiki/Toxicity_class

    Indian toxicity label system Toxicity symbol for European toxicity class I and class II. Toxicity class refers to a classification system for pesticides that has been created by a national or international government-related or -sponsored organization.

  7. p-Cresol - Wikipedia

    en.wikipedia.org/wiki/P-cresol

    ch 3 c 6 h 4 so 3 h + 2 naoh → ch 3 c 6 h 4 oh + na 2 so 3 + h 2 o Other methods for the production of p -cresol include chlorination of toluene followed by hydrolysis. In the cymene-cresol process, toluene is alkylated with propene to give p -cymene , which can be oxidatively dealkylated in a manner similar to the cumene process .

  8. γ-Butyrolactone - Wikipedia

    en.wikipedia.org/wiki/Γ-butyrolactone

    γ-Butyrolactone (GBL) or gamma-butyrolactone is an organic compound with the formula O=CO(CH 2) 3. It is a hygroscopic, colorless, water-miscible liquid with a weak characteristic odor. It is the simplest 4-carbon lactone. It is mainly used as an intermediate in the production of other chemicals, such as N-methyl-2-pyrrolidone. [5]

  9. Thymol - Wikipedia

    en.wikipedia.org/wiki/Thymol

    Thymol (also known as 2-isopropyl-5-methylphenol, IPMP), C 10 H 14 O, is a natural monoterpenoid phenol derivative of p-Cymene, isomeric with carvacrol.It occurs naturally in the oil of thyme, and it is extracted from Thymus vulgaris (common thyme), ajwain, [4] and various other plants as a white crystalline substance of a pleasant aromatic odor and strong antiseptic properties.

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