Identification | Back Directory | [Name]
DICHLORAMINE T | [CAS]
473-34-7 | [Synonyms]
DICHLORAMINE T Dichloroamine-T DICHLORAMINE T HYDRATE Benzyl p-sulfondichloramide P-TOLUENESULFONDICHLORAMIDE N,N-Dichloro-p-tolylsulfonamide N,N-DICHLORO-P-TOLUENESULFONAMIDE N,N-Dichloro-4-toluenesulfonamide N,N-Dichloro-p-toluenesulphonamide n,n-dichlorotoluene-4-sulphonamide p-toluenesulfonic acid dichloramide N,N-Dichloro-p-toluenesulfonamide 97% N,N-Dichloro-p-methylbenzenesulfonamide N,N-dichloro-4-methylbenzenesulfonamide n,n-dichloro-4-methyl-benzenesulfonamid N,N-Dichloro-4-methylbenzenesulphonamide N,N-dichloro-4-methyl-benzenesulfonamide Benzenesulfonamide,N,N-dichloro-4-methyl- BENZENESULPHONAMIDE,N,N-DICHLORO-4-METHYL- DichloraMine T, N,N-Dichloro-p-toluenesulfonaMide N,N-Dichloro-p-toluenesulfonamide
p-Toluenesulfondichloramide | [EINECS(EC#)]
207-462-4 | [Molecular Formula]
C7H7Cl2NO2S | [MDL Number]
MFCD00058929 | [MOL File]
473-34-7.mol | [Molecular Weight]
240.11 |
Hazard Information | Back Directory | [Uses]
Germicide. | [Purification Methods]
Crystallise it from pet ether (b 60-80o) or CHCl3/pet ether. Dry it in air <55o and store in the dark. It is soluble in CHCl3 (~1:1), *C6H6 (~1:1) and CCl4 (~1:2.5). It is a germicide and antibacterial as it readily liberates chlorine, and it should not smell strongly of chlorine; otherwise it should be purified. Alternatively dissolve ~15g of reagent in 75mL of hot acetic acid and precipitate it by addition of 37mL of N/10 bleaching powder solution (NaOCl), filter off, wash it with a dilute solution of the latter, dry as above (m 78-84o) and recrystallise it. “Sharp drying” will decompose it. [Orton & Bradfield J Chem Soc 993 1927, Krauss & Crede J Am Chem Soc 39 2720 1917, Soper J Chem Soc 1899 1924.] [see also chloramine-T (monochloramine T Na salt) in “Metal-organic Compounds”, Chapter 5]. [Beilstein 11 H I07, 11 I 27, 11 II 63, 11 III 301.] |
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