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  2. 1,2,4-Butanetriol - Wikipedia

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

    1,2,4-Butanetriol is an organic compound with the formula HOCH 2 CH(OH)CH 2 CH 2 OH. It is an colorless, odorless, hygroscopic , oily liquid. Containing three alcohol groups, it is classified as a polyol , similar to glycerol and erythritol .

  3. Thermal oxidizer - Wikipedia

    en.wikipedia.org/wiki/Thermal_oxidizer

    VAMTOX units have a system of valves and dampers that direct the air flow across one or more ceramic filled bed(s). On start-up, the system preheats by raising the temperature of the heat exchanging ceramic material in the bed(s) at or above the auto-oxidation temperature of methane 1,000 °C (1,830 °F), at which time the preheating system is ...

  4. 2,4,6-Trinitrobenzoic acid - Wikipedia

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

    2,4,6-Trinitrobenzoic acid is prepared by oxidation of 2,4,6-trinitrotoluene (TNT). It is formed by oxidation of TNT and nitric acid with chlorate [2] and with dichromate. [3] Upon heating, 2,4,6-trinitrobenzoic acid undergoes decarboxylation to give 1,3,5-trinitrobenzene. [4]

  5. 2,4-Dinitrotoluene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrotoluene

    2,4-Dinitrotoluene (DNT) or dinitro is an organic compound with the formula C 7 H 6 N 2 O 4. This pale yellow crystalline solid is well known as a precursor to trinitrotoluene (TNT) but is mainly produced as a precursor to toluene diisocyanate .

  6. 2,4,6-Tri-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tri-tert-butylphenol

    [5] 2,4,6-tri-tert-butylphenol is also found as a by-product in the synthesis of the disubstitution products 2,4-DTBP and 2,6-DTBP, which are more widely used antioxidants. [2] Synthese von 2,4,6-Tri-tert-butylphenol mit Isobuten. A synthesis of 2,4,6-tri-tert-butylphenol has been described that is also suitable as a teaching experiment.

  7. Fast protein liquid chromatography - Wikipedia

    en.wikipedia.org/wiki/Fast_protein_liquid...

    Fast protein liquid chromatography (FPLC) is a form of liquid chromatography that is often used to analyze or purify mixtures of proteins. As in other forms of chromatography, separation is possible because the different components of a mixture have different affinities for two materials, a moving fluid (the mobile phase) and a porous solid (the stationary phase).

  8. Toxicity class - Wikipedia

    en.wikipedia.org/wiki/Toxicity_class

    The system is based on LD50 determination in rats, thus an oral solid agent with an LD50 at 5 mg or less/kg bodyweight is Class Ia, at 5–50 mg/kg is Class Ib, LD50 at 50–2000 mg/kg is Class II, and at LD50 at the concentration more than 2000 mg/kg is classified as Class III. Values may differ for liquid oral agents and dermal agents. [1]

  9. Liquid–liquid extraction - Wikipedia

    en.wikipedia.org/wiki/Liquid–liquid_extraction

    Some extraction systems are able to extract metals by both the solvation and ion exchange mechanisms; an example of such a system is the americium (and lanthanide) extraction from nitric acid by a combination of 6,6'-bis-(5,6-dipentyl-1,2,4-triazin-3-yl)-2,2'-bipyridine and 2-bromohexanoic acid in tert-butyl benzene. At both high- and low ...