enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    It is advised to check the references for photos of reaction results. [1] Reagent testers might show the colour of the desired substance while not showing a different colour for a more dangerous additive. [2] For this reason it is essential to use multiple different tests to show all adulterants.

  3. Reagent testing - Wikipedia

    en.wikipedia.org/wiki/Reagent_testing

    Reagent testing is one of the processes used to identify substances contained within a pill, usually illicit substances. With the increased prevalence of drugs being available in their pure forms, the terms "drug checking" or "pill testing" [1] may also be used, although these terms usually refer to testing with a wider variety of techniques covered by drug checking.

  4. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkanes with more than three carbon atoms can be arranged in various ways, forming structural isomers.The simplest isomer of an alkane is the one in which the carbon atoms are arranged in a single chain with no branches.

  5. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  6. Slow strain rate testing - Wikipedia

    en.wikipedia.org/wiki/Slow_strain_rate_testing

    These test results are compared to those for similar tests in a, known to be inert, environment. A 50-year history of the SSRT has recently been published by its creator. [1] The test has also been standardized [2] [3] and two ASTM symposia devoted to it. [4] [5]

  7. 2-Ethylhexanol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylhexanol

    2-Ethylhexanol (abbreviated 2-EH) is an organic compound with the chemical formula C H 3 CH 2 CH 2 CH 2 CH(CH 2 CH 3)CH 2 OH. It is a branched, eight-carbon chiral alcohol . It is a colorless liquid that is poorly soluble in water but soluble in most organic solvents.

  8. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

  9. 2-ethylhexane - Wikipedia

    en.wikipedia.org/?title=2-ethylhexane&redirect=no

    Language links are at the top of the page across from the title.