Sodium dichloroisocyanurate

Base Information

• Chemical Name: Sodium dichloroisocyanurate
• CAS No.: 2893-78-9
• Molecular Formula: C3Cl2N3NaO3
• Molecular Weight: 219.947
• Hs Code.: Oral rat LD50: 1420 mg/kg
• Mol file: 2893-78-9.mol

Synonyms:Hi-Lite 60G;CDB 63;Oniachlor 60;ACL 56;Actisan;ACL 60;Clearon;Clearon CDB;Dikonit;Hi-Lite G 60GW;1,3-dichloro-1,3,5-triazinane-2,4,6-trione;Clearon CDB 56;Prisept;Fi Clor Clearon;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3- dichloro-,sodium salt;Oxidan DCN/WSG;Crente;Surchlor GR 60;CDB Clearon;Neochlor 60P;Basolan DC;SDIC (Sodium Dichloroisocyanurate);DCCNa;Sodium Dichloroisocyanu rate(DCCNa);troclosene sodium;Dichloroisocyanuric acid sodium salt;SDIC;Sodium dichloro-s-triazinetrione;Sodium Dichloro iso cyanurate;water purification tablets;Sodium Dichloroisocyanurate ( SDIC );Dichloroisocyanuric Acid;

Chemical Property of Sodium dichloroisocyanurate

Chemical Property:

• Appearance/Colour: white crystalline powder
• Vapor Pressure: 7.05E-05mmHg at 25°C
• Melting Point: 225 °C
• Boiling Point: 306.7 °C at 760 mmHg
• Flash Point: 139.3 °C
• PSA: 79.95000
• Density: 2.06 g/cm³
• LogP: -0.44740
• Storage Temp.: 0-6°C
• Sensitive.: Moisture Sensitive
• Water Solubility.: 30g/100ml (25 ºC)

Purity/Quality:

60% ^*data from raw suppliers

DichloroisocyanuricAcidSodiumSalt ^*data from reagent suppliers

Safty Information:

• Pictogram(s): O,Xn,N
• Hazard Codes: O,Xn,N,E
• Statements: 8-22-31-36/37-50/53-2
• Safety Statements: 8-26-41-60-61-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Description: Sodium dichloroisocyanurate(NaDCC) is the sodium salt of a chlorinated hydroxytriazine and is used as a source of free available chlorine, in the form of hypochlorous acid, for the disinfection of water. It is widely used as a stable source of chlorine for the disinfection of swimming pools and in the food industry. It is also used as a means of disinfecting drinking-water, primarily in emergencies, when it provides an easy-to-use source of free chlorine, and, more recently, as the form of chlorine for household point-of-use water treatment.
• Uses: Sodium dichloroisocyanurate, the sodium salt of a chlorinated hydroxytriazine, is used as a source of free available chlorine (in the form of hypochlorous acid, HOCl) for disinfecting drinking water.Sodium dichloroisocyanurate can be manufactured either as the anhydrous salt or as the dihydrate. Anhydrous sodium dichloroisocyanurate contains about 63% free available chlorine. When this compound is added to water, it is rapidly hydrolyzed to release free available chlorine, establishing a complex series of equilibria involving six chlorinated and four non-chlorinated isocyanurates. As free available chlorine is consumed on reacting with organic material in the water, chloroisocyanurates rapidly dissociate and continue to release free chlorine.The use of sodium dichloroisocyanurate as a source of freely available chlorine is not expected to lead to greater production of by-products than does the use of elemental chlorine. Sodium Dichloroisocyanurate (SDIC) widely applied for the sterilization of swimming pool and drinking water, or fighting against infectious diseases, or act as disinfectant in raising silkworm, livestock, poultry and fish. Other applications of SDIC are found in wool shrinkage, textile bleaching, and industrial circulating water cleaning. SDIC is normally supplied in powder and granular, tablets are also available on request. Stabilised chlorine granular (dichlor) are used very widely to chlorinate swimming pool water. Sodium dichloroisocyanurate can be used as a reagent for N-monochlorination and dehydrochlorination of amino esters. It is also a reagent for chlorination to detect ammonium via formation of colored zebra-bands in a detecting tube.

Technology Process of Sodium dichloroisocyanurate

There total 1 articles about Sodium dichloroisocyanurate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ sode de l'acide trichloroisocyanurique (2893-78-9)

Guidance literature:

Mononatriumcyanurat + HOCl.;

Reference yield: 67.9%

sode de l'acide trichloroisocyanurique (2893-78-9) → potassium dibromoisocyanurate (15114-46-2)

Guidance literature:

With potassium bromide; In water; for 24h;

Reference yield:

sode de l'acide trichloroisocyanurique (2893-78-9) + 2-n-butyl-4,5-di-(hydroxymethyl)-1H-imidazole (136317-69-6) → 2-n-butyl-4-chloro-5-hydroxymethylimidazole (79047-41-9)

Guidance literature:

In 1,4-dioxane; ethanol;

Downstream raw materials:

2-n-butyl-4-chloro-5-hydroxymethylimidazole

potassium dibromoisocyanurate

Refernces