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  2. Acrolein - Wikipedia

    en.wikipedia.org/wiki/Acrolein

    Acrolein (systematic name: propenal) is the simplest unsaturated aldehyde. It is a colorless liquid with a foul and acrid aroma. It is a colorless liquid with a foul and acrid aroma. The smell of burnt fat (as when cooking oil is heated to its smoke point ) is caused by glycerol in the burning fat breaking down into acrolein.

  3. Sigma-Aldrich - Wikipedia

    en.wikipedia.org/wiki/Sigma-Aldrich

    Sigma Advanced Genetic Engineering (SAGE) Labs is a division within Sigma-Aldrich that specializes in genetic manipulation of in vivo systems for special research and development applications. It was formed in 2008 to investigate zinc finger nuclease technology and its application for disease research models.

  4. 1,3-Propanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Propanediol

    1,3-Propanediol is mainly produced by the hydration of acrolein. An alternative route involves the hydroformylation of ethylene oxide to form 3-hydroxypropionaldehyde. The aldehyde is subsequently hydrogenated to give 1,3-propanediol. Biotechnological routes are also known. [2] Two other routes involve bioprocessing by certain micro-organisms:

  5. File:Cr-Ac-OH-MSDS SigmaAldrich.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Cr-Ac-OH-MSDS_Sigma...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  6. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

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

  7. 3,9-Divinyl-2,4,8,10-tetraoxaspiro (5.5)undecane - Wikipedia

    en.wikipedia.org/wiki/3,9-Divinyl-2,4,8,10-tetra...

    Condensation products from propenal and pentaerythritol were first described in 1950. [4] [5] The synthesis is carried using a general synthesis method for acetals at acid pH (pH 3-5) by reacting an alcohol with an excess of aldehyde, which is stabilized with hydroquinone in the case of propenal, which tends to polymerize at elevated temperature.