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This solid compound, available as tablets, is widely used as a disinfectant, to sterilize drinking water, swimming pools, tableware, farming installations, and air; and as an industrial deodorant. It is also used for bleaching textiles. [2] Halazone, or 4-((dichloroamino)sulfonyl)benzoic acid, (HOOC)(C 6 H 4) (SO 2)(NCl 2). This compound was ...
Fluorobenzaldehyde can be used as a synthetic intermediate because the fluorine can be replaced via oxidation reaction. [1] Due to the aldehyde group, the fluorobenzaldehydes can be used to make a variety of schiff base compounds through a condensation reaction, some of which have antimicrobial properties. [2] [3]
2-Chloro-6-fluorobenzaldehyde is prepared by oxidation of 2-chloro-6-fluorotolulene by chromyl chloride. [3] It reacts with sodium hydroxide to give a mixture of 2-chloro-6-fluorobenzene and 6-chlorosalicaldehyde. [4] 2-Chloro-6-fluorobenzaldehyde is used in the production of the antiseptics dicloxacillin and flucloxacillin.
4-Chlorobenzaldehyde (o-Chlorobenzaldehyde) is an organic compound with the formula ClC 5 H 4 CHO. It is one of three isomeric monochlorinated benzaldehydes . Preparation
Sodium hypochlorite is an alkaline inorganic chemical compound with the formula Na O Cl (also written as NaClO). It is commonly known in a dilute aqueous solution as bleach or chlorine bleach. [4] It is the sodium salt of hypochlorous acid, consisting of sodium cations (Na +) and hypochlorite anions (− OCl, also written as OCl − and ClO −).
2-Chlorobenzaldehyde (o-chlorobenzaldehyde) is an organic compound with the formula ClC 5 H 4 CHO. It is one of three isomeric monochlorinated benzaldehyde. 3-Chlorobenzaldehyde and 4-chlorobenzaldehyde are the other isomers. Whereas benzaldehyde is prone to autoxidation, the 2-chloro derivatives are more air-stable.
[4] Inorganic chloramines are produced by the reaction of ammonia and hypochlorous acid or chlorine. An urban legend claims that mixing household bleach (aqueous sodium hypochlorite) with ammonia-based cleaners releases chlorine gas or mustard gas; in reality, the gas produced by the reaction is a mixture of inorganic chloramines.
NOBS is the main bleach activator used in the U.S.A. and Japan. [4] Compared to TAED , which is the predominant bleach activator used in Europe, NOBS is efficient at much lower temperatures. At 20 °C NOBS is 100 times more soluble than TAED in water. [ 5 ]