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  3. Dichloroisocyanurate sodium

Dichloroisocyanurate sodium is a synthetic organochlorine compound belonging to triazine derivatives, and is commonly used as a disinfectant and biocide. Dichloroisocyanurate sodium can release hypochlorous acid to inactivate waterborne bacteria, viruses, helminths and protozoa, and can act as a hypochlorous acid reservoir to provide sustained biocidal protection.

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Dichloroisocyanurate sodium

Dichloroisocyanurate sodium Chemical Structure

CAS No. : 2893-78-9

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Description

Dichloroisocyanurate sodium is a synthetic organochlorine compound belonging to triazine derivatives, and is commonly used as a disinfectant and biocide. Dichloroisocyanurate sodium can release hypochlorous acid to inactivate waterborne bacteria, viruses, helminths and protozoa, and can act as a hypochlorous acid reservoir to provide sustained biocidal protection[1][2].

In Vitro

Sodium dichloroisocyanurate exhibits excellent antimicrobial activity against a variety of Gram-positive bacteria, Gram-negative bacteria and fungi, and its activity is not affected by temperature or pH[1].
Sodium dichloroisocyanurate exhibits excellent disinfection activity against various microorganisms on fresh vegetables[1].
Sodium dichloroisocyanurate (30 min) eliminates all coliforms and E. coli from low-turbidity water, and reduces the viable count in raw river water by 1.8-2.8 log units[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Dichloroisocyanurate sodium (0.4-10.0 mg/m3; whole-body inhalation; 6 hours/day, 7 days/week; 90 days) causes concentration-dependent pulmonary and systemic effects in Sprague-Dawley/Crl:CD rats, with a no observed adverse effect concentration (NOAEC) of 2.0 mg/m3 for both sexes[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague-Dawley/Crl:CD (7 weeks old after 6 days of acclimatization; 10 males/females per exposure group, 5 males/females per recovery group)[2]
Dosage: 0.4 mg/m3; 2.0 mg/m3; 10.0 mg/m3
Administration: whole-body inhalation; 6 hours/day, 7 days/week; 90 days; 14-day recovery (10.0 mg/m3 group only)
Result: Exhibited signs of lung inflammation, eosinophilic granules observed in the nasal cavity, hyperplasia of mucous cells, atrophy/degeneration of the tracheal epithelium, and thickening of the walls of the alveolar ducts in high dose group.
Molecular Weight

220.95

Formula

C3HCl2N3NaO3

CAS No.
Appearance

Solid

SMILES

[Na].O=C1NC(=O)N(Cl)C(=O)N1Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature, keep dry and cool

In solvent -80°C 1 year
-20°C 6 months
Purity & Documentation
References
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Product Name:
Dichloroisocyanurate sodium
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HY-B2180
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