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Usage

Uses

Used in Plastic Industry:
Dithiobiuret is used as a plasticizer to enhance the flexibility, workability, and processability of various types of plastics. Its incorporation into the polymer matrix improves the overall performance and durability of the end product.
Used in Rubber Industry:
In the rubber industry, Dithiobiuret serves as a rubber accelerator, promoting faster and more efficient curing of rubber compounds. This leads to improved mechanical properties and reduced production time, making it a valuable additive in the manufacturing of rubber products.
Used in Pesticide Manufacturing:
Dithiobiuret is utilized as an intermediate in the production of various pesticides. Its chemical properties make it a suitable candidate for the synthesis of active ingredients that can effectively control pests and protect crops.

Air & Water Reactions

pH of the saturated aqueous solution is 5.8.

Reactivity Profile

Dithiobiuret is a thioamide, which may behave as a weak acid in solution and therefore will react with base foeming salts with production of heat. Dithiobiuret may react with acids and reducing agents to form toxic hydrogen sulfide gas. This may be vigorous depending on the nature of the reducing agent. Organic amides/imides react with azo and diazo compounds to generate toxic gases. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Health Hazard

The material is highly toxic. It may cause respiratory failure.

Fire Hazard

When heated to decomposition, Dithiobiuret emits highly toxic fumes of oxides of sulfur and nitrogen.

Safety Profile

Poison by ingestion and intraperitoneal routes. When heated to decomposition it emits highly toxic fumes of SOx and NOx.

InChI:InChI=1/C6H3FN2/c7-5-2-1-3-9-6(5)4-8/h1-3H

Upstream product

• 127099-85-8 N-Cyanoguanidine 
• 31111-24-7 1-t-Butyl-2,4-dithiobiuret 
• 67754-13-6 1-t-Butyl-4-S-t-butyliso-2-thiobiuret 
• 21867-64-1 1-n-propylpiperazine 
• 30013-32-2 3-dimethylamino-1,2,4-dithiazole-5-thione 
• 142-25-6 N,N',N'-trimethylenediamine 
• 127099-85-8 dicyandiamide 
• 1934-75-4 sodium dicyanamide 

Downstream Products

• 1843-12-5 2,2'-imino-bis-4,4'-diphenylthiazole 
• 28077-65-8 3,5-diamino-1,2,4-dithiazolium chloride 
• 7364-95-6 3,5-diamino-1,2,4-dithiazolium bromide 
• 30805-32-4 6-phenyl-1,3,5-triazinane-2,4-dithione 
• 61851-94-3 6-(4-methoxyphenyl)-2,4-dithioxo-1,3,5-triazinane 
• 30886-13-6 6-phenyl-1H-[1,3,5]triazine-2,4-dithione 
• 5333-35-7 propylidene-dithiobiuret 
• 6635-76-3 N-(4-p-Chlorophenyl-2-thiazolyl)thiourea 
• 107523-24-0 bis-[4-(3-nitro-phenyl)-thiazol-2-yl]-amine 
• 7713-93-1 bis-(4,5-diphenyl-thiazol-2-yl)-amine 
• 14015-63-5 <4-(4-Nitro-phenyl)-thiazol-2-yl>-thioharnstoff 
• 7713-89-5 bis-[4-(4-nitro-phenyl)-thiazol-2-yl]-amine 
• 7709-31-1 N'-(4-phenylthiazol-2-yl)thiourea 
• 7713-86-2 Bis-<4-(4-brom-phenyl)-thiazol-2-yl>-amin 

Relevant academic research and scientific papers

PRODUCTION METHOD OF THIOUREA

PROBLEM TO BE SOLVED: To provide a production method of thiourea, which has high safety, can afford thiourea by a simple production facility and method, and further can reduce a production cost. SOLUTION: The production method of thiourea comprises the steps of: reacting a compound such as dicyandiamide and the like and hydrogen sulfide and the like to obtain a compound such as dithiobiuret and the like; and reacting a compound such as dithiobiuret and the like with ammonia, ammonium salts, and the like. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Pesticidal dithiazolium salts

Dithiazolium salts of one of the following formulas: SPC1 Where R, r1, r2, and R3 are certain organic radicals, the ring EQU1 contains 5-8 atoms, and A, E, and G are alkylene, And their use as pesticides. An exemplary compound: Hydrochloric acid salt of 3-dimethylamino-5-(4-methylpiperazin-l-yl)-1,2,4-dithiazolium chloride.