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  1. Oct 26, 2020 · Triphenylmethanol. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Triphenylmethanol or triphenylcarbinol, is an organic compound, a tertiary alcohol with the formula (C6H5)3COH. It is sometimes abbreviated as TrOH or Ph3COH .

  2. Aldrich-134848; Triphenylmethanol 0.97; CAS No.: 76-84-6; Synonyms: Triphenylcarbinol; Trityl alcohol; Linear Formula: (C6H5)3COH; Empirical Formula: C19H16O; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.

  3. Jun 21, 2023 · Triphenylmethanol (Zidovudine EP Impurity D) is a triaryl methane derivative as antiproliferative agent. Uses. Triphenylmethanol is used as a reagent in the research laboratory. It acts as an intermediate in the production of the commercially useful triarylmethane dyes. It is used in the preparation of triphenylmethane.

  4. Triphenylmethanol Revision Date 24-Dec-2021 Component CAS No Weight % Benzenemethanol, .alpha.,.alpha.-diphenyl- 76-84-6 97 4. First-aid measures Eye Contact Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes. Skin Contact Wash off immediately with soap and plenty of water while removing all contaminated clothes and shoes.

  5. Apr 22, 2024 · Objective. To familiarize the student with the preparation of Grignard reagents and their reaction with carbonyl compounds to form alcohols, in particular the synthesis of triphenylmethanol (an alcohol) from bromobenzene. Triphenylmethanol (triphenylcarbinol) LZTRCELOJRDYMQ-UHFFFAOYSA-N. 3D Structure.

  6. Our Story. CAS Future Leaders. CAS Innovation Incubator. Press Releases. Careers. Quickly confirm chemical names, CAS Registry Numbers®, structures or basic physical properties by searching compounds of general interest or leveraging an API connection.

  7. Mar 17, 2024 · Objective. Experiment 7 is a group experiment. You will work in a small group to carry out variations of the Grignard reaction with phenyl magnesium bromide and benzophenone to form triphenylmethanol and to answer the focus questions below.

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