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  2. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4] Since the reaction requires a free carbonyl group, only "reducing sugars" participate.

  3. List of reagent testing color charts - Wikipedia

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

    Reagent test Alcohols: Forms Lucas test in alcohols is a test to differentiate between primary, secondary, and tertiary alcohols. Alkaloids: Forms Froehde Liebermann Mandelin Marquis Mayer's Mecke Simon's: Amines, and amino acids: Forms Folin's: Barbiturates: Class Dille–Koppanyi Zwikker: Benzodiazepines: Class Zimmermann: Phytocannabinoids ...

  4. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Hydrazones are converted to azines when used in the preparation of 3,5-disubstituted 1H-pyrazoles, [12] a reaction also well known using hydrazine hydrate. [ 13 ] [ 14 ] With a transition metal catalyst , hydrazones can serve as organometallic reagent surrogates to react with various electrophiles.

  5. 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.

  6. Molisch's test - Wikipedia

    en.wikipedia.org/wiki/Molisch's_test

    Molisch test (using α-napthol) indicating a positive result (see purple ring). Molisch's test is a sensitive chemical test, named after Austrian botanist Hans Molisch, for the presence of carbohydrates, based on the dehydration of the carbohydrate by sulfuric acid or hydrochloric acid to produce an aldehyde, which condenses with two molecules of a phenol (usually α-naphthol, though other ...

  7. Instruments used in obstetrics and gynecology - Wikipedia

    en.wikipedia.org/wiki/Instruments_used_in...

    - Used in Premalignant lesions of the cervix. Its provides a specimen. Uterine dressing forceps: FemCerv Endocervical Sampler: The FDA cleared disposable FemCerv endocervical Sampler can be used to biopsy the endocervical canal during colposcopyor the evaluation of abnormal uterine bleeding. FemCerv is intended to collect a 360° Endocervical ...

  8. Ellman's reagent - Wikipedia

    en.wikipedia.org/wiki/Ellman's_reagent

    This reaction is rapid and stoichiometric, with the addition of one mole of thiol releasing one mole of TNB. The TNB 2− is quantified in a spectrophotometer by measuring the absorbance of visible light at 412 nm, using an extinction coefficient of 14,150 M −1 cm −1 for dilute buffer solutions, [4] [5] and a coefficient of 13,700 M −1 cm −1 for high salt concentrations, such as 6 M ...

  9. Organozinc chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozinc_chemistry

    The organozinc reagent is generated via an oxidative addition into the alkyl halide. The reaction produces a primary, secondary, or tertiary alcohol via a 1,2-addition . The Barbier reaction is advantageous because it is a one-pot process: the organozinc reagent is generated in the presence of the carbonyl substrate.