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  2. 1,4-Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobenzene

    1,4-Dichlorobenzene (1,4-DCB, p-DCB, or para-dichlorobenzene, sometimes abbreviated as PDCB or para) is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring.

  3. Dichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Dichlorobenzene

    1,2-Dichlorobenzene or ortho-dichlorobenzene; 1,3-Dichlorobenzene or meta-dichlorobenzene; 1,4-Dichlorobenzene or para-dichlorobenzene. All three isomers are colorless chlorobenzenes with the formula C 6 H 4 Cl 2. They differ structurally based on where the two chlorine atoms are attached to the ring.

  4. 1,2-Dichlorobenzene - Wikipedia

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

    1,2-Dichlorobenzene, or orthodichlorobenzene (ODCB), is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colourless liquid is poorly soluble in water but miscible with most organic solvents.

  5. Chlorobenzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene_(data_page)

    Specific heat capacity, c p? J/(mol K) Liquid properties Std enthalpy change of formation, Δ f H o liquid: 11.1 kJ/mol Standard molar entropy, S o liquid? J/(mol K) Specific heat capacity, c p: 150.1 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: 52.0 kJ/mol Standard molar entropy, S o gas? J/(mol K) Specific heat ...

  6. 1,4-Dichloro-2-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichloro-2-nitrobenzene

    Disperse Yellow 42, a popular dye for polyesters, is derived from 1,4-dichloro-2-nitrobenzene. [1]1,4-Dichloro-2-nitrobenzene is an organic compound with the formula C 6 H 3 Cl 2 NO 2.

  7. 1,2,4-Trichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4-Trichlorobenzene

    The LD50 (oral, rats) is 756 mg/kg. Animal studies have shown that 1,2,4-trichlorobenzene affects the liver and kidney, and is possibly a teratogen. [4] There is no regulated occupational exposure limit for chemical exposure, but the National Institute for Occupational Safety and Health recommends no greater exposure than 5 ppm, over an 8-hour workday.

  8. 1,2-Dichloro-4-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloro-4-nitrobenzene

    The nitration of 1,2-dichlorobenzene mainly produces 1,2-dichloro-4-nitrobenzene, together with smaller amounts of the 3-nitro isomer. It can also be prepared by chlorination of 1-chloro-4-nitrobenzene. [1] One of the chlorides is reactive toward nucleophiles.

  9. C6H4Cl2 - Wikipedia

    en.wikipedia.org/wiki/C6H4Cl2

    The molecular formula C 6 H 4 Cl 2 (molar mass: 147.00 g/mol) may refer to: 1,2-Dichlorobenzene; 1,3-Dichlorobenzene; 1,4-Dichlorobenzene; Dichlorofulvenes;