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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. Bis(2,4,5-trichloro-6-(pentyloxycarbonyl)phenyl)oxalate ...

    en.wikipedia.org/wiki/Bis(2,4,5-trichloro-6...

    Bis[2,4,5-trichloro-6-(pentyloxycarbonyl)phenyl]oxalate (also known as bis(2,4,5-trichloro-6-carbopentoxyphenyl) oxalate or CPPO) is an organic compound with the formula (C 5 H 11 O 2 CC 6 HCl 3 O) 2 C 2 O 2. A white solid, it is classified as a diester of oxalic acid. It is an active ingredient for the chemiluminescence in glowsticks. [1]

  6. Phenyl isocyanate - Wikipedia

    en.wikipedia.org/wiki/Phenyl_isocyanate

    The molecule consists of a phenyl ring attached to the isocyanate functional group. It is a colourless liquid that reacts with water. Phenyl isocyanate has a strong odor and tearing vapours, therefore it has to be handled with care. Characteristic of other isocyanates, it reacts with amines to give ureas. [2]

  7. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    CH 2 =CHCH 2 Cl + Na 2 S 2 O 3 → CH 2 =CHCH 2 S 2 O 3 Na + NaCl CH 2 =CHCH 2 S 2 O 3 Na + NaCN → CH 2 =CHCH 2 SCN + Na 2 SO 3. Sulfenyl chlorides (RSCl) also convert to thiocyanates. Aryl thiocyanates are traditionally produced by the Sandmeyer reaction, which involves combining copper(I) thiocyanate and diazonium salts: [3]

  8. Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Trichlorophenol

    Trichlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1] Different isomers of trichlorophenol exist according to which ring positions on the phenol contain chlorine atoms. 2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position.

  9. TCPO - Wikipedia

    en.wikipedia.org/wiki/TCPO

    TCPO, or bis(2,4,6-trichlorophenyl) oxalate, is a chemical used in some types of glow sticks and is a key chemical in many chemiluminescent reactions. TCPO is classified as damaging to human organs and toxic if inhaled with an inhalable toxicity of 3.02 mg/L and oral toxicity LD50 of 820 mg/kg (rat).