 | |
| Names | |
|---|---|
| Preferred IUPAC name 1,3-Benzothiazole-2(3H)-thione | |
| Other names Mercapto-2-benzothiazole; 2-MBT | |
| Identifiers | |
| |
3D model (JSmol) | |
| 508810 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.005.216 |
| EC Number |
|
| KEGG | |
| UNII | |
| |
| |
| Properties | |
| C7H5NS2 | |
| Molar mass | 167.24 g·mol−1 |
| Appearance | white solid |
| Melting point | 177–181 °C (351–358 °F; 450–454 K) |
| Hazards | |
| GHS labelling: | |
  | |
| Warning | |
| H317,H410 | |
| P261,P272,P273,P280,P302+P352,P321,P333+P313,P363,P391,P501 | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
2-Mercaptobenzothiazole is anorganosulfur compound with the formulaC6H4(NH)SC=S. A white solid, it is a reagent inorganic synthesis[1] and, notably, for thesulfur vulcanization of rubber.[2]
The molecule is planar in shape, with a C=S double bond, so the namemercaptobenzothiazole is a misnomer; a more appropriate name could bebenzothiazoline-2-thione. Solution measurements byNMR spectroscopy could not identify the presence of thethioltautomer that the name implies, instead it exists as athione/dithiocarbamate and the hydrogen appears on the nitrogen in the gas-phase, solid state, and in solution.[3] Theory indicates that the thione tautomer is about 39 kJ/mol lower in energy than the thiol, and a hydrogen-bonded dimer of the thione has even lower energy.[4] At alkaline pH greater than 7 the deprotonatedthiolate form is most abundant. A protonated form could not be observed in the pH range 2-11.[5]
The compound has been produced by many methods. Industrially, MBT is synthesised by the Kelly process (U.S. Pat. No. 1,631,871), whereby Sulfur, aniline and carbon disulfide are reacted under elevated pressure at elevated temperatures in a batch reactor. The industrial route entails the high temperature reaction ofaniline andcarbon disulfide in the presence of sulfur, which proceeds by this idealized equation:[4][1]
The traditional route is the reaction of2-aminothiophenol and carbon disulfide:
This method was developed by the discoverer of the compound, A. W. Hoffmann. Other routes developed by Hoffmann include the reactions of carbon disulfide with 2-aminophenol and ofsodium hydrosulfide with chlorobenzothiazole.[6] Further synthetic advances were reported in the 1920s that included demonstration that phenyldithiocarbamates pyrolyze to benzothiazole derivative.[7]
Industrially, MBT purification consists of a reprecipitation, wherein crude MBT is dissolved in sodium hydroxide solution, tar-like by-products are decanted off, filtered off or extracted. The aqueous sodium MBT solution is subjected to a further oxidative treatment, if appropriate; the MBT is then precipitated using sulfuric acid and filtered off (cf. German Patent 2,258,484). Unless captured, H2S escapes from the reaction upon completion of the reaction.
The mechanism of the reaction and identification of by-products was clarified byNeal Stuart Isaacs andFyaz Mahmood Daud Ismail, his postdoctoral colleague, working at Reading University between 1989 and 1991[8]This process has been converted from batch to flow and optimised using chemometric methods. Shandong Yanggu Huatai Co., Ltd., is operating this optimised process at a 10,000-ton-scale MBT production plant. The simulation results allowed optimisation to a green synthesis of MBT, with optimal industrial production and, therefore, reducing pollution from this important industrial process.[9]
The compound is insoluble in water but dissolves upon the addition of base, reflecting deprotonation.[10]Treatment withRaney nickel results in monodesulfurization, givingbenzothiazole:[4]
The benzo ring undergoes electrophilic aromatic substitution at the position para to nitrogen.[4]
S-alkylation of mercaptobenzothiazole gives thioether, which can be oxidized to the sulfone. This sequence sets the stage for theModified Julia olefination.
Oxidation gives mercaptobenzothiazole disulfide. This disulfide reacts withamines to givesulfenamide derivatives such 2-morpholinodithiobenzothiazole. These compounds are used insulphur vulcanization, where they act as accelerators.
disulfide.svg)
Using 2-mercaptobenzothiazole, rubber vulcanizes with less sulfur and at milder temperatures, both factors give a stronger product. This effect was reported by workers at Pirelli and at Goodyear Tire & Rubber.[2]Lorin B. Sebrell won the 1942Charles Goodyear Medal for his work on mercaptobenzothiazole.
In polymerization, it finds use as a radical polymerization inhibitor,chain transfer agent, reforming agent, and additive forphotoinitiators.[11]
The compound has also been used in the past in the gold-mining industry for thefroth flotation of gold from ore residue as part of the extraction process.[12]
Sodium salt is used as a biocide and preservative in adhesives (especially based on latex, starch, casein, and animal glues), paper, textiles. Often found together with sodiumdimethyldithiocarbamate as e.g. Vancide 51. Zinc salt is used as a secondary accelerator in latex foam vulcanization.[13]
It can be added to oil-basedhydraulic fluids, heat-transfer fluids (oils,antifreezes),cutting fluids and other mixtures as acorrosion inhibitor, effective forcopper andcopper alloys.[14]
It is also used in veterinary dermatology.[15]
Inelectroplating it is used as a brightener forcopper sulfate baths, at about 50-100 milligrams/liter. Also can be added to silver cyanide baths.[14]
Mercaptobenzothiazole has a low toxicity in mice, with anLD50 of > 960 mg/kg.[4]
In 2016, it was identified by theWorld Health Organization as probably carcinogenic to humans.[16]
It causesallergic contact dermatitis.[17] The derivative morpholinylmercaptobenzothiazole is a reported allergen in protective gloves, including latex,nitrile, andneoprene gloves.[18]
It becomes air-borne as a result of wear on car tires, and is able to beinhaled.[19] Evidence suggests that benzothiazolesbiodegrade readily.[20]
Benzothiazoles were long ago found to strongly influence the course of thevulcanization of rubber.[21]
