enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 2-Phenylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Phenylphenol

    2-Phenylphenol, or o-phenylphenol, is an organic compound. In terms of structure, it is one of the monohydroxylated isomers of biphenyl. [2] [3] It is a white solid. It is a biocide used as a preservative with E number E231 and under the trade names Dowicide, Torsite, Fungal, Preventol, Nipacide and many others.

  3. Spray nozzle - Wikipedia

    en.wikipedia.org/wiki/Spray_nozzle

    Spray nozzles can have one or more outlets; a multiple outlet nozzle is known as a compound nozzle. Multiple outlets on nozzles are present on spray balls, which have been used in the brewing industry for many years for cleaning casks and kegs. [2] Spray nozzles range from those for heavy duty industrial uses to light duty spray cans or spray ...

  4. Sprayer - Wikipedia

    en.wikipedia.org/wiki/Sprayer

    Sprayers range in size from man-portable units (typically backpacks with spray guns) to trailed sprayers that are connected to a tractor, to self-propelled units similar to tractors with boom mounts of 4–30 feet (1.2–9.1 m) up to 60–151 feet (18–46 m) in length depending on engineering design for tractor and land size. [1]

  5. o-Toluidine - Wikipedia

    en.wikipedia.org/wiki/O-Toluidine

    o-Toluidine (ortho-toluidine) is an organic compound with the chemical formula CH 3 C 6 H 4 NH 2. It is the most important of the three isomeric toluidines. It is a colorless liquid although commercial samples are often yellowish. It is a precursor to the herbicides metolachlor and acetochlor. [2]

  6. 1,2-Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichlorobenzene

    2 → C 6 H 4 Cl 2 + HCl. The reaction also affords the 1,4- and small amounts of the 1,3-isomer. The 1,4- isomer is preferred over the 1,2- isomer due to steric hindrance. The 1,3- isomer is uncommon because it is a meta- compound, while chlorine, like all halogens, is an ortho/para-director in terms of electrophilic aromatic substitution.

  7. o-Cresol - Wikipedia

    en.wikipedia.org/wiki/O-cresol

    ortho-Cresol (IUPAC name: 2-methylphenol, also known as 2-hydroxytoluene or ortho-Toluenol) is an organic compound with the formula CH 3 C 6 H 4 (OH). It is a colourless solid that is widely used intermediate in the production of other chemicals. It is a derivative of phenol and is an isomer of p-cresol and m-cresol. [3]

  8. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Ortho effect is an organic chemistry phenomenon where the presence of a chemical group at the at ortho position or the 1 and 2 position of a phenyl ring, relative to the carboxylic compound changes the chemical properties of the compound.

  9. Paraquat - Wikipedia

    en.wikipedia.org/wiki/Paraquat

    Paraquat (trivial name; / ˈ p ær ə k w ɒ t /), or N,N′-dimethyl-4,4′-bipyridinium dichloride (systematic name), also known as methyl viologen, is a toxic organic compound with the chemical formula [(C 6 H 7 N) 2]Cl 2.