2492-26-4 Usage
Uses
1. Used in Copper Corrosion Inhibition:
Sodium mercaptobenzothiazole is used as a copper corrosion inhibitor to prevent the degradation of copper and its alloys. It helps in maintaining the integrity and performance of copper-based materials in various applications.
2. Used in Acid Copper Plating:
In the plating industry, sodium mercaptobenzothiazole is used as a plasticizer and photometer for acid copper plating. It enhances the flexibility and adhesion of the plated layer, ensuring a uniform and high-quality finish.
3. Used in Water Treatment:
Sodium mercaptobenzothiazole is employed as a water treatment agent, where it acts as a corrosion inhibitor. It helps in protecting water infrastructure and equipment from corrosion, thereby extending their lifespan and ensuring efficient water distribution.
4. Used in Chemical Intermediates:
Sodium mercaptobenzothiazole is also used as a chemical intermediate in the synthesis of various compounds. Its unique properties make it a valuable component in the production of different chemicals.
5. Used in Bactericides and Fungicides (Potential Application):
The biological activity of sodium mercaptobenzothiazole indicates its potential use as a bactericide or fungicide. It may be utilized in the development of products that help control the growth of bacteria and fungi, contributing to improved hygiene and sanitation.
Air & Water Reactions
Sensitive to prolonged exposure to air. Water soluble.
Reactivity Profile
SODIUM 2-MERCAPTOBENZOTHIAZOL reacts vigorously with oxidizing materials (e.g. hydroperoxides). Liberates heat in contact with strong mineral acids or acid fumes .
Health Hazard
Contact with moisture in the body by inhalation may yield sodium hydroxide (corrosive) and 2-mercaptabenzothiazole, an irritant. Contact with the eyes caused opacity or ulceration of the cornea, inflammation of the iris, redness and swelling of the conjunctiva and partial eversion of the eye lids, and destruction or irreversible tissue change in 24 hours or less (rabbit). A dose of 2,500 mg/kg applied to the skin caused severe depression, cold extremities, appetite loss; 4 of 10 died. Exposure of the skin to 1,250 mg/kg caused a severe degree of skin injury. The skin was burned in 24 hours with formation of hard eschar at 1-2 weeks; 1 of 10 rabbits died. Ingestion caused tremors, convulsions, severe depression and hemaluria in male rats. Ingestion of 312.5 mg/kg: 1 of 5 male rats die on day 2; 625 mg/kg: 2 of 5 died within 3-5 minutes; 1,250 mg/kg: 3 of 5 died within 3-5 minutes; 2,500 mg/kg: 100% mortality within 3-5 minutes. Hemorrhage of the stomach occurred in all rats that died.
Safety Profile
Moderately toxic by ingestion. When heated to decomposition it emits very toxic fumes of NOx, SOx, and NazO. See also MERCAPTANS.
Regulations
Sodium 2-mercaptobenzothiazole was first registered as a pesticide in the United States in 1949 in an industrial preservative product. Currently, only one product is registered, for use in wood and paper/paperboard treatment and as a preservative in metal working cutting fluids, emulsions, textiles and pastes.sodium and zinc salts of 2-mercaptobenzothiazole
Check Digit Verification of cas no
The CAS Registry Mumber 2492-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2492-26:
(6*2)+(5*4)+(4*9)+(3*2)+(2*2)+(1*6)=84
84 % 10 = 4
So 2492-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NS2.Na/c9-7-8-5-3-1-2-4-6(5)10-7;/h1-4H,(H,8,9);/q;+1
2492-26-4Relevant articles and documents
A chemical looping technology for the synthesis of 2,2′-dibenzothiazole disulfide
Tian, Jiaxin,Jiayu Hu,Wang, Kai,Deng, Jian,Luo, Guangsheng
, p. 2778 - 2785 (2020/06/17)
A novel chemical looping technology for the synthesis of 2,2′-dibenzothiazole disulfide (MBTS) with zero emissions has been developed. Through chemical cycling between carbonate and bicarbonate in the reaction system, the insoluble 2-mercaptobenzothiazole (MBT) can become soluble in the aqueous phase of sodium carbonate and then be oxidized efficiently by hydrogen peroxide and the absorption of CO2 with high selectivity. The mother liquor can be totally recycled by the desorption of CO2 without any generation of salt-containing wastewater. With the new synthesis technology, the product has high purity and reaches the standard of a superior product that can be applied as a vulcanization accelerator. When 5.0 wt% hydrogen peroxide was added dropwise over 40 min at 50 °C, the conversion ratio of MBT was over 98%. The mother liquor was recycled 5 times and no side-products were found. The whole process is clean and pollution-free, which greatly reduces the burden of hazardous waste treatment and brings great environmental benefits.
NOVEL METHOD FOR PREPARING ROSUVASTATIN, INTERMEDIATE COMPOUNDS USEFUL FOR PREPARING SAME, AND METHOD FOR PREPARING SAME
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Page/Page column 15, (2012/04/23)
The present invention relates to novel intermediate compounds used in preparing Rosuvastatin or the pharmaceutically acceptable salts thereof, to a method for preparing same, and to a method for preparing Rosuvastatin or the pharmaceutically acceptable salts thereof from the intermediates. The preparation method of the present invention has the effect of providing Rosuvastatin hemi-calcium salts with an excellent yield rate.
NOVEL METHOD FOR PREPARING ROSUVASTATIN, INTERMEDIATE COMPOUNDS USEFUL FOR PREPARING SAME, AND METHOD FOR PREPARING SAME
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Page/Page column 10, (2012/06/16)
The present invention relates to novel intermediate compounds used in preparing Rosuvastatin or the pharmaceutically acceptable salts thereof, to a method for preparing same, and to a method for preparing Rosuvastatin or the pharmaceutically acceptable salts thereof from the intermediates. The preparation method of the present invention has the effect of providing Rosuvastatin hemi-calcium salts with an excellent yield rate.
