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  2. Benzoyl peroxide (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_peroxide_(data_page)

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source such as eChemPortal search query 94-36-0, and follow its directions.

  3. Benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_peroxide

    Benzoyl peroxide is usually prepared by treating hydrogen peroxide with benzoyl chloride under alkaline conditions. 2 C 6 H 5 COCl + H 2 O 2 + 2 NaOH → (C 6 H 5 CO) 2 O 2 + 2 NaCl + 2 H 2 O. The oxygen–oxygen bond in peroxides is weak. Thus, benzoyl peroxide readily undergoes homolysis (symmetrical fission), forming free radicals: (C 6 H 5 ...

  4. 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.

  5. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Benzoyl peroxide and hydrogen peroxide are used as bleaching and "maturing" agents for treating flour to make its grain release gluten more easily; the alternative is letting the flour slowly oxidize by air, which is too slow for the industrialized era. Benzoyl peroxide is an effective topical medication for treating most forms of acne.

  6. Polyester resin - Wikipedia

    en.wikipedia.org/wiki/Polyester_resin

    Cobalt salts are the most common type of promoter used. Common radical initiators used are organic peroxides such as benzoyl peroxide or methyl ethyl ketone peroxide. [8] Polyester resins are thermosetting and, as with other resins, cure exothermically. The use of excessive initiator especially with a catalyst present can, therefore, cause ...

  7. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    Standard conditions for using NBS in allylic and/or benzylic bromination involves refluxing a solution of NBS in anhydrous CCl 4 with a radical initiator—usually azobisisobutyronitrile or benzoyl peroxide, irradiation, or both to effect radical initiation.

  8. Peroxide value - Wikipedia

    en.wikipedia.org/wiki/Peroxide_value

    The peroxide value is defined as the amount of peroxide oxygen per 1 kilogram of fat or oil. Traditionally this was expressed in units of milliequivalents, although in SI units the appropriate option would be in millimoles per kilogram (N.B. 1 milliequivalents = 0.5 millimole; because 1 mEq of O2 =1 mmol/2 of O2 =0.5 mmol of O2, where 2 is valence).

  9. Erythromycin/benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Erythromycin/benzoyl_peroxide

    Using an oil-free face moisturizer in conjunction with erythromycin/benzoyl peroxide is recommended. Erythromycin/benzoyl peroxide was approved by the US Food and Drug Administration in 1984. [ 2 ] On March 30, 2004, a generic form of Benzamycin was released by pharmaceutical company Atrix Laboratories .