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  2. DBNPA - Wikipedia

    en.wikipedia.org/wiki/DBNPA

    DBNPA or 2,2-dibromo-3-nitrilopropionamide is a quick-kill biocide that easily hydrolyzes under both acidic and alkaline conditions. It is preferred for its instability in water as it quickly kills and then quickly degrades to form a number of products, depending on the conditions, including ammonia, bromide ions, dibromoacetonitrile, and dibromoacetic acid. [2]

  3. Diquat - Wikipedia

    en.wikipedia.org/wiki/Diquat

    A pesticide can only be used legally according to the directions on the label that is included at the time of the sale of the pesticide. The purpose of the label is "to provide clear directions for effective product performance while minimizing risks to human health and the environment".

  4. BCDMH - Wikipedia

    en.wikipedia.org/wiki/BCDMH

    1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH or bromochlorodimethylhydantoin) is a chemical structurally related to hydantoin.It is a white crystalline compound with a slight bromine and acetone odor and is insoluble in water, but soluble in acetone.

  5. Bronopol - Wikipedia

    en.wikipedia.org/wiki/Bronopol

    Bronopol is used in consumer products as an effective preservative agent, as well as a wide variety of industrial applications (almost any industrial water system is a potential environment for bacterial growth, leading to slime and corrosion problems - in many of these systems bronopol can be a highly effective treatment).

  6. Talk:DBNPA - Wikipedia

    en.wikipedia.org/wiki/Talk:DBNPA

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  7. Dipropylene glycol - Wikipedia

    en.wikipedia.org/wiki/Dipropylene_glycol

    Dipropylene glycol finds many uses as a plasticizer, an intermediate in industrial chemical reactions, as a polymerization initiator or monomer, and as a solvent.Its low toxicity and solvent properties make it an ideal additive for perfumes and skin and hair care products.

  8. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    Cyanogen bromide is often used to immobilize proteins by coupling them to reagents such as agarose for affinity chromatography. [5] Because of its simplicity and mild pH conditions, cyanogen bromide activation is the most common method for preparing affinity gels.

  9. File:DBNPA-3D-spacefill.png - Wikipedia

    en.wikipedia.org/wiki/File:DBNPA-3D-spacefill.png

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