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  2. Potassium dichromate - Wikipedia

    en.wikipedia.org/wiki/Potassium_dichromate

    Patch test. In 2005–06, potassium dichromate was the 11th-most-prevalent allergen in patch tests (4.8%). [12] Potassium dichromate is one of the most common causes of chromium dermatitis; [13] chromium is highly likely to induce sensitization leading to dermatitis, especially of the hand and forearms, which is chronic and difficult to treat ...

  3. Chemical oxygen demand - Wikipedia

    en.wikipedia.org/wiki/Chemical_oxygen_demand

    Most commonly, a 0.25 N solution of potassium dichromate is used for COD determination, although for samples with COD below 50 mg/L, a lower concentration of potassium dichromate is preferred. In the process of oxidizing the organic substances found in the water sample, potassium dichromate is reduced (since in all redox reactions, one reagent ...

  4. Zenker's fixative - Wikipedia

    en.wikipedia.org/wiki/Zenker's_fixative

    Zenker is usually made with 50g of mercuric chloride, 25g of potassium dichromate, 10g of sodium sulfate (decahydrate) and distilled water to complete 1000 ml. Before use, 5 ml glacial acetic acid is added to 100 ml of the solution. Both the stock solution and the complete Zenker fixative are stable for many years.

  5. Chromyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chromyl_chloride

    The chromyl chloride test involves heating a sample suspected to contain chlorides with potassium dichromate and concentrated sulfuric acid. If a chloride is present, chromyl chloride forms, its presence being indicated by the formation of red smoke. Otherwise, no red smoke will obviously appear.

  6. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    An example is potassium dichromate, which does not pass the dangerous goods test of an oxidizing agent. The U.S. Department of Transportation defines oxidizing agents specifically. There are two definitions for oxidizing agents governed under DOT regulations. These two are Class 5; Division 5.1(a)1 and Class 5; Division 5.1(a)2. Division 5.1 ...

  7. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  8. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    For oxidations to the aldehydes and ketones, two equivalents of chromic acid oxidize three equivalents of the alcohol: 2 HCrO 4 − + 3 RR'C(OH)H + 8 H + + 4 H 2 O → 2 [Cr(H 2 O) 6] 3+ + 3 RR'CO. For oxidation of primary alcohols to carboxylic acids, 4 equivalents of chromic acid oxidize 3 equivalents of the alcohol. The aldehyde is an ...

  9. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.