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TBP is a solvent and plasticizer for cellulose esters such as nitrocellulose and cellulose acetate, similarly to tricresyl phosphate. It is also used as a flame retardant for cellulose fabrics such as cotton. [7] [8] It forms stable hydrophobic complexes with some metals; these complexes are soluble in organic solvents as well as supercritical ...
Microbial metabolism in products treated with TBP is known to produce 2,4,6-tribromoanisole (TBA), [9] which has a musty odor. In 2010 and 2011, Pfizer and Johnson & Johnson voluntarily recalled some products due to TBA odors from wooden pallets which were treated with TBP. [10] [11] [12] [13]
TBP is involved in DNA melting (double strand separation) by bending the DNA by 80° (the AT-rich sequence to which it binds facilitates easy melting). The TBP is an unusual protein in that it binds the minor groove using a β sheet. Another distinctive feature of TBP is a long string of glutamines in the N-terminus of the protein.
Red oil is defined as a substance of varying composition formed when an organic solution, typically tri-n-butyl phosphate (TBP, an agent used for extracting heavy metals in nuclear reprocessing plants) and its diluent, comes in contact with concentrated nitric acid at a temperature above 120 °C.
Tributylphosphine is the organophosphorus compound with the chemical formula P(CH 2 CH 2 CH 2 CH 3) 3, often abbreviated as PBu 3.It is a tertiary phosphine.It is an oily liquid at room temperature, with a nauseating odor.
The degree of DNA bending is species and sequence dependent. For example, one study used the adenovirus TATA promoter sequence (5'-CGCTATAAAAGGGC-3') as a model binding sequence and found that human TBP binding to the TATA box induced a 97° bend toward the major groove while the yeast TBP protein only induced an 82° bend. [21]
The synthetic opioid is what’s known as a partial agonist — meaning there’s a limit to how much the medication can affect people who use it. In the U.S., buprenorphine is mainly sold under the brand name Suboxone, in which form it’s combined with naloxone, the drug that can reverse the effects of an overdose.
The reaction can be used for the synthesis of 2,6-di-tert-butyl-4-methoxyphenol, which is frequently used as an antioxidant. Synthese von 2,6-Di- tert -butyl-4-methoxyphenol aus 2,4,6-TTBP 2,4,6-TTBP is used as stabilizers , free-radical scavengers and antioxidants in technical applications, such as in fuels , hydraulic fluids and lubricating ...