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  2. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride was first prepared in 1852 by French chemist Charles Gerhardt by treating potassium acetate with phosphoryl chloride. [4]Acetyl chloride is produced in the laboratory by the reaction of acetic acid with chlorodehydrating agents such as phosphorus trichloride (PCl 3), phosphorus pentachloride (PCl 5), sulfuryl chloride (SO 2 Cl 2), phosgene, or thionyl chloride (SOCl 2).

  3. Chloroacetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chloroacetyl_chloride

    The major use of chloroacetyl chloride is as an intermediate in the production of herbicides in the chloroacetanilide family including metolachlor, acetochlor, alachlor and butachlor; an estimated 100 million pounds are used annually. Some chloroacetyl chloride is also used to produce phenacyl chloride, another chemical intermediate, also used ...

  4. Flammability limit - Wikipedia

    en.wikipedia.org/wiki/Flammability_limit

    Lower flammability limit (LFL): The lowest concentration (percentage) of a gas or a vapor in air capable of producing a flash of fire in the presence of an ignition source (arc, flame, heat). The term is considered by many safety professionals to be the same as the lower explosive level (LEL). At a concentration in air lower than the LFL, gas ...

  5. Flammability diagram - Wikipedia

    en.wikipedia.org/wiki/Flammability_diagram

    Flammability diagrams show the control of flammability in mixtures of fuel, oxygen and an inert gas, typically nitrogen. Mixtures of the three gasses are usually depicted in a triangular diagram, known as a ternary plot. Such diagrams are available in the speciality literature. [ 1][ 2][ 3] The same information can be depicted in a normal ...

  6. Isocyanate - Wikipedia

    en.wikipedia.org/wiki/Isocyanate

    Isocyanate. The isocyanate functional group. In organic chemistry, isocyanate is the functional group with the formula R−N=C=O. Organic compounds that contain an isocyanate group are referred to as isocyanates. An organic compound with two isocyanate groups is known as a diisocyanate.

  7. Thionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Thionyl_chloride

    Thionyl chloride is an inorganic compound with the chemical formula SOCl 2.It is a moderately volatile, colourless liquid with an unpleasant acrid odour.Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes (50,000 short tons) per year being produced during the early 1990s, [5] but is occasionally also used as a solvent.

  8. Oxalyl chloride - Wikipedia

    en.wikipedia.org/wiki/Oxalyl_chloride

    Oxalyl chloride. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ?) Oxalyl chloride is an organic chemical compound with the formula Cl−C (=O)−C (=O)−Cl. This colorless, sharp-smelling liquid, the di acyl chloride of oxalic acid, is a useful reagent in organic synthesis.

  9. Iron(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Iron(III)_chloride

    Infobox references. Iron (III) chloride describes the inorganic compounds with the formula Fe Cl 3 (H 2 O) x. Also called ferric chloride, these compounds are some of the most important and commonplace compounds of iron. They are available both in anhydrous and in hydrated forms which are both hygroscopic.