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  2. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    Benzophenone is a naturally occurring organic compound with the formula (C 6 H 5) 2 CO, generally abbreviated Ph 2 CO. Benzophenone has been found in some fungi, fruits and plants, including grapes. [4] It is a white solid with a low melting point and rose-like odor [5] that is soluble in organic solvents. Benzophenone is the simplest ...

  3. 4,4'-Dihydroxybenzophenone - Wikipedia

    en.wikipedia.org/wiki/4,4'-dihydroxybenzophenone

    Safety data sheet (SDS) MSDS by Fisher Scientific Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. Oxybenzone - Wikipedia

    en.wikipedia.org/wiki/Oxybenzone

    Oxybenzone or benzophenone-3 or BP-3 (trade names Milestab 9, Eusolex 4360, Escalol 567, KAHSCREEN BZ-3) is an organic compound belonging to the class of aromatic ketones known as benzophenones. It takes the form of pale-yellow crystals that are readily soluble in most organic solvents.

  6. Michler's ketone - Wikipedia

    en.wikipedia.org/wiki/Michler's_ketone

    p-Dimethylaminobenzophenone is related to Michler's ketone, but with only one amine. [5] Auramine O, a dye, is a salt of the iminium cation [(CH 3) 2 NC 6 H 4] 2 CNH 2 +.Michler's thione, [(CH 3) 2 NC 6 H 4] 2 CS, is prepared by treatment of Michler's ketone with hydrogen sulfide in the presence of acid or sulfideing auramine O. [6] Hydride reduction of Michler's ketone gives 4,4'-bis ...

  7. Benzophenone imine - Wikipedia

    en.wikipedia.org/wiki/Benzophenone_imine

    Benzophenone imine can be prepared by the thermal decomposition of benzophenone oxime: [2]. 2 (C 6 H 5) 2 C=NOH → (C 6 H 5) 2 C=NH + (C 6 H 5) 2 C=O. Benzophenone imine can also be synthesized by addition of phenylmagnesium bromide to benzonitrile followed by careful hydrolysis (lest the imine be hydrolyzed): [3]

  8. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Distillation data. 6 Spectral data. 7 Safety data ...

  9. Category:Benzophenones - Wikipedia

    en.wikipedia.org/wiki/Category:Benzophenones

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