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  2. Butylated hydroxytoluene - Wikipedia

    en.wikipedia.org/wiki/Butylated_hydroxytoluene

    BHT is used as a preservative ingredient in some foods. With this usage BHT maintains freshness or prevents spoilage; it may be used to decrease the rate at which the texture, color, or flavor of food changes. [25] Some food companies have voluntarily eliminated BHT from their products or have announced that they were going to phase it out. [26]

  3. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene is widely used in the paint, dye, rubber, chemical, glue, printing, and pharmaceutical industries as a solvent. [38] Nail polish, paintbrush cleaners, and stain removers may contain toluene. Manufacturing of explosives (TNT) uses it as well. Toluene is also found in cigarette smoke and car exhaust.

  4. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    Synthetic sulfonates are the most widely used detergents, as industrial oil, emulsifiers, demulsifiers, rust inhibitors, dispersants, surfactants for enhanced oil recovery, ore-floatation agents, and wetting agents, among others. LABs such as alkylbenzene, dialkylbenzene, and alkyltoluene are most commonly used to prepare sulfonate detergents.

  5. Toluene toxicity - Wikipedia

    en.wikipedia.org/wiki/Toluene_toxicity

    Hippuric acid has long been used as an indicator of toluene exposure; [14] however, there appears to be some doubt about its validity. [15] There is significant endogenous hippuric acid production by humans; which shows inter- and intra-individual variation influenced by factors such as diet, medical treatment, alcohol consumption, etc. [15] This suggests that hippuric acid may be an ...

  6. Chain transfer - Wikipedia

    en.wikipedia.org/wiki/Chain_transfer

    In polymer chemistry, chain transfer is a polymerization reaction by which the activity of a growing polymer chain is transferred to another molecule: [1] [2] + + where • is the active center, P is the initial polymer chain, X is the end group, and R is the substituent to which the active center is transferred.

  7. 4-Toluenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Toluenesulfonyl_chloride

    4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl. This white, malodorous solid is a reagent widely used in organic synthesis. [2] Abbreviated TsCl or TosCl, it is a derivative of toluene and contains a sulfonyl chloride (−SO 2 Cl) functional group.

  8. Organogels - Wikipedia

    en.wikipedia.org/wiki/Organogels

    The kinetic and statistical methods model gel formation with different mathematical approaches. As of 2014 [update] most researchers used statistical methods, as the equations derived thereby are less cumbersome and contain variables to which specific physical meanings can be attached, thus aiding in the analysis of gel formation theory. [ 5 ]

  9. 4-tert-Butylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-tert-Butylcatechol

    It is added as a stabilizer and polymerisation inhibitor to butadiene, styrene, [5] vinyl acetate, divinylbenzene [6] and other reactive monomer streams. [7] TBC is also used as a stabilizer in the manufacture of polyurethane foam. [8] It also can be used as an antioxidant for synthetic rubber, polymers and oil derivatives. [7]