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  2. Biphenyl - Wikipedia

    en.wikipedia.org/wiki/Biphenyl

    Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene [4] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl .

  3. Diphenic acid - Wikipedia

    en.wikipedia.org/wiki/Diphenic_acid

    It is the most studied of several isomeric dicarboxylic acids of biphenyl. It is a white solid that can be prepared in the laboratory from anthranilic acid via the diazonium salt. [1] It is the product of the microbial action on phenanthrene. [2] The compound forms a variety of coordination polymers. [3] It also exhibits atropisomerism.

  4. Polychlorinated biphenyl - Wikipedia

    en.wikipedia.org/wiki/Polychlorinated_biphenyl

    Polychlorinated biphenyls ... which even presently results in paper contamination. [30] ... synthesized the first PCB in a laboratory. [94] Since then, large amounts ...

  5. Biphenyl 2,3-dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Biphenyl_2,3-dioxygenase

    The 4 substrates of this enzyme are biphenyl, NADH, H +, and O 2, whereas its two products are (1S,2R)-3-phenylcyclohexa-3,5-diene-1,2-diol and NAD +. This enzyme belongs to the family of oxidoreductases , specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen.

  6. Biphenyl synthase - Wikipedia

    en.wikipedia.org/wiki/Biphenyl_synthase

    In enzymology, a biphenyl synthase (EC 2.3.1.177) is an enzyme that catalyzes the chemical reaction: . 3 malonyl-CoA + benzoyl-CoA 4 CoA + 3,5-dihydroxybiphenyl + 4 CO 2. Thus, the two substrates of this enzyme are malonyl-CoA and benzoyl-CoA, whereas its three products are CoA, 3,5-dihydroxybiphenyl, and CO 2.

  7. Polybrominated biphenyl - Wikipedia

    en.wikipedia.org/wiki/Polybrominated_biphenyl

    Exposure to the coplanar stereoisomer 3,3',4,4',5,5'-hexabromobiphenyl (but not the non-coplanar stereoisomer) in genetically susceptible mice is known to cause immunotoxicity and disorders related to the central nervous system, and even at doses as low as 2.5 mg/kg, excess neonatal fatalities are observed (LD 50 is from 5–10 mg/kg). [1]

  8. 2,2′-Bipyridine - Wikipedia

    en.wikipedia.org/wiki/2,2′-Bipyridine

    Biphenyl: Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...

  9. Industrial Bio-Test Laboratories - Wikipedia

    en.wikipedia.org/wiki/Industrial_Bio-Test...

    Industrial Bio-Test Laboratories (IBT Labs) was an American industrial product safety testing laboratory. [1] [2] [3] IBT conducted significant quantities of research for pharmaceutical companies, chemical manufacturers and other industrial clients; at its height during the 1950s, 1960s, and 1970s, IBT operated the largest facility of its kind and performed more than one-third of all ...