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Thiourea, N,N'-dioctyl-, also known as N,N'-dioctyl-thiourea, is a sulfur-containing organic compound derived from thiourea. It is a versatile chemical with applications in various industries, including mining, metallurgy, textile, and rubber. Known for its selective extraction and separation capabilities, it plays a crucial role in the recovery of precious metals from ores and mineral deposits.

109-40-0

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109-40-0 Usage

Uses

Used in Mining and Metallurgy Industry:
Thiourea, N,N'-dioctylis used as a metal extractant for selectively extracting and separating precious metals such as gold, silver, and platinum from ores and mineral deposits. Its unique properties enable efficient recovery of valuable metals, making it an essential component in the mining and metallurgy processes.
Used in Flotation Process:
In the flotation process, Thiourea, N,N'-dioctylis used as a collector to separate valuable minerals from gangue materials. Its ability to selectively bind to specific minerals aids in the efficient separation and concentration of desired minerals, improving the overall efficiency of the mining process.
Used in Textile Industry:
Thiourea, N,N'-dioctylis used as a curing agent and accelerator in the textile industry. It enhances the curing process of certain materials, improving their performance and durability. Its presence in the textile industry contributes to the production of high-quality textiles with enhanced properties.
Used in Rubber Industry:
Similarly, in the rubber industry, Thiourea, N,N'-dioctylis utilized as a curing agent and accelerator. It plays a vital role in the production of rubber goods by promoting the curing process, resulting in rubber products with improved strength and elasticity.
However, it is crucial to handle and dispose of Thiourea, N,N'-dioctylwith care due to its potential environmental and health hazards. Proper safety measures and disposal methods should be followed to minimize any adverse effects on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 109-40-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109-40:
(5*1)+(4*0)+(3*9)+(2*4)+(1*0)=40
40 % 10 = 0
So 109-40-0 is a valid CAS Registry Number.

109-40-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Di-n-octylthiourea

1.2 Other means of identification

Product number -
Other names N,N'-dioctyl-oxalamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109-40-0 SDS

109-40-0Upstream product

109-40-0Downstream Products

109-40-0Relevant academic research and scientific papers

Cerium ammonium nitrate-catalyzed aerobic oxidative coupling of dithiocarbamates: Facile synthesis of thioureas and bis(aminothiocarbonyl)disulfides

Li, Tian-Tian,Song, Xiang-Hai,Wang, Mei-Shuang,Ma, Ning

, p. 40054 - 40060 (2014/12/10)

Diverse disubstituted and trisubstituted thioureas were synthesized by the condensation of dithiocarbamate TEA (or DABCO) salts and amines using cerium ammonium nitrate (CAN) as a catalyst in high yields at room temperature. It is a one-pot method and it is unnecessary to isolate isothiocyanates. This reaction probably took place through nucleophilic addition of amines to isothiocyanates, which were generated by oxidative coupling of dithiocarbamates and the following decomposition of bis(aminothiocarbonyl)disulfides. When secondary amines and CS2served as the reactants, bis(aminothiocarbonyl)disulfides were obtained via tandem nucleophilic addition/oxidative coupling reactions in moderate to excellent yields. In all the coupling reactions, the oxidant was air and CAN possibly acted as an SET catalyst.

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