PRODUCTS

2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS)

2,2'-Dibenzothiazyl disulfide (MBTS) is used as an accelerator in the rubber industry.
2,2'-Dibenzothiazyl disulfide (MBTS) is added to many types of rubber before vulcanization.
2,2'-Dibenzothiazyl disulfide (MBTS)'s industry uses also include fillers, fuels and fuel additives, intermediates, process regulator, propels and blowing agents.

CAS Number: 120-78-5
EC Number: 204-424-9
MDL number: MFCD00022874
Molecular Formula: C14H8N2S4
Molecular Weight: 332.47 g/mol

SYNONYMS:
Benzothiazole,2,2′-dithiobis-, 2,2′-Dithiobis[benzothiazole], Benzothiazole disulfide, Benzothiazolyl disulfide, 2-Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Dibenzothiazyl disulfide, Dibenzthiazyl disulfide, MBTS, MBTS rubber accelerator, 2-Mercaptobenzothiazole disulfide, Royal MBTS, Thiofide, Dibenzothiazolyl disulfide, Di-2-benzothiazolyl disulfide, 2,2′-Dibenzothiazolyl disulfide, Pneumax DM, Vulcafor MBTS, Vulkacit DM, Ekagom GS, 2,2′-Benzothiazyl disulfide, 2-Benzothiazyl disulfide, Vulkacit DM/C, Accel TM, Nocceler DM, Merasulf MBTS, Nocceler DM-PO, DBTD, Wobezit DM, Sanceler DM, 2,2′-Benzothiazolyl disulfide, Accel DM, Vulkacit DM/MG, 2,2′-Dibenzothiazole disulfide, NSC 677459, Soxinol DM, Vulkafil ZN 96TT11, Perkacit MBTS, Thiofide MBTS, DM, DM (accelerator), Tiazol 2MBS, NSC 2, 1,2-Bis(2-benzothiazolyl) disulfide, Bis(benzothiazol-2-yl)disulfide, Accelerator DM, Oricel DM, Quick Accelerator 200, Dibenzothiophene disulfide, Sanceler DM-G, OCITS, Naugex MBTS, Dispraktol K 16, DM 80 (vulcanizer), DM 80, Thiazole 2MBS, Accelerator MBTS, 2,2′-Benzothiazole disulfide, Rhenogran MBTS 70, Rhenogran MBTS 80, MBTS 75, Rhenogran MBTS 75, Sunsine Mets, Thanecure ZM, DZ 42, Sunsine MBTS, 1,2-Bis(benzo[d]thiazol-2-yl)disulfane, 2,2′-Dithiobis-1,3-benzothiazole, Promoter DM, Rhenogran MBTS, 2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole, MBTS MG, 109767-80-8, 137497-18-8, 186983-60-8, 258278-97-6, 2293932-50-8, Altax, Benzothiazol-2-yl disulfide, Benzothiazole disulfide, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(benzothiazolyl) disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Dibenzothiazolyl disulfide, Ekagom GS, MBTS, MBTS Rubber Accelerator, Pneumax DM, Royal MBTS, Thiofide, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, 2-Benzothiazolyl disulfide, 2-Mercaptobenzothiazole disulfide, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dithiobis[benzothiazole], Accel TM, Di-2-benzothiazolyl disulfide, Dibenzoylthiazyl disulfide, 2-Mercaptobenzothiazyl disulfide, Dibenzothiazolyl disulphide, Dwusiarczek dwubenzotiazylu, USAF CY-5, USAF EK-5432, Vulkacit DM/MGC, Dibenzothiazole disulfide, Dibenzthiazyl disulfide, Mercaptobenzthiazyl ether, Naugex MBT, Perkacit MBTS, 2-Benzothiazyl disulfide, Dibenzothiazyl disulfide, Sanceler DM, di(benzothiazol-2-yl) disulphide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dibenzothiazolyl disulfide, 2,2'-Dibenzothiazolyl disulphide, 2,2'-Dithiobisbenzothiazole, 2,2'-Dithiobis-benzothiazole, Dithiobis(2-benzothiazole), Di(benzothiazol-2-yl) disulfide, Di(benzothiazol-2-yl) disulphide, Di(benzothiazole-2-yl) disulphide, 2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole, 2-Mercaptobenzothiazole Disulfide, MBTS, DM, Vulkacit DM, Rubber Accelerator MBTS, MBTS,2,2, Accelerator, 1,2-bis(benzo[d]thiazol-2-yl)disulfane, DIBENZOTHIAZOLE DISULFIDE, benzothiazolyl, 2-Mercaptobenzothi, BENZOTHIAZYL DISULFIDE, Benzothiazole disulfide, 2-BENZOTHIAZOLYL DISULFIDE, 2,2’-Dithiobisbenzothiazole, 1,2-Bis(2-benzothiazolyl) disulfide, 2,2'-Benzothiazolyl disulfide, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazole disulfide, 2,2'-Dibenzothiazolyl disulfide, 2,2'-Dithiobis[benzothiazole], 2-Benzothiazolyl disulfide, 2-Benzothiazyl disulfide, 2-Mercaptobenzothiazole disulfide, Accel DM, Accel TM, Accelerator DM, Altax, Benzothiazole disulfide, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Bis(benzothiazol-2-yl)disulfide, DBTD, DM, DM (accelerator), Di-2-benzothiazolyl disulfide, Dibenzothiazolyl disulfide, Dibenzothiazyl disulfide, Dibenzothiophene disulfide, Dibenzthiazyl disulfide, Ekagom GS, MBTS, MBTS rubber accelerator, Merasulf MBTS, NSC 2, NSC 677459, Naugex MBTS, Nocceler DM, Nocceler DM-PO, OCITS, Oricel DM, Perkacit MBTS, Pneumax DM, Quick Accelerator 200, Royal MBTS, Sanceler DM, Sanceler DM-G, Soxinol DM, Thiofide, Thiofide MBTS, Tiazol 2MBS, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, Vulkacit DM/MG, Vulkafil ZN 96TT11, Wobezit DM, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dithiobis[benzothiazole], Altax, Benzothiazyl disulfide, Dibenzothiazyl disulfide, MBTS, Mercaptobenzthiazyl ether, Naugex MBT, Thiofide, Vulkacit DM, Di(benzothiazol-2-yl)disulfide, Dibenzothiazole disulfide, 2,2′-Dithiobis(benzothiazole), Thiofid, MBTS (2,2'-Dithiobisbenzothiazole), AKOS001022311, BIS(2-BENZOTHIAZYL) DISULPHIDE, Tox21_111106_1, 2,2'-DIBENZOTHIAZOLE DISULFIDE, 2,2'-Dithiobis(benzothiazole), 99%, AM91095, CS-W009852, DB14201, NSC-677459, DIBENZOTHIAZYL DISULFIDE [VANDF], NCGC00091238-01, NCGC00091238-03, 2,2'-DITHIOBISBENZOTHIAZOLE [MI], AC-11588, LS-14263, 2,2'-disulfanediylbis(1,3-benzothiazole), WLN: T56 BN DSJ CSS-CT56 BN DSJ, D0538, NS00005023, 2,2'-DIBENZOTHIAZYL DISULFIDE [HSDB], D77699, EN300-7399114, SR-01000944767, 2-(1,3-benzothiazol-2-yldithio)-1,3-benzothiazole, Q2795423, SR-01000944767-1, 1,2-Bis(2-benzothiazolyl) disulfide, 1,2-Bis(benzo[d]thiazol-2-yl)disulfane, 2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole, 2-Benzothiazolyl disulfide, 2-Benzothiazyl disulfide, 2-Mercaptobenzothiazole disulfide, 2,2′-Benzothiazole disulfide, 2,2′-Benzothiazolyl disulfide, 2,2′-Benzothiazyl disulfide, 2,2′-Dibenzothiazole disulfide, 2,2′-Dibenzothiazolyl disulfide, 2,2′-Dithiobis-1,3-benzothiazole, 2,2′-Dithiobis[benzothiazole], Benzothiazole disulfide, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Bis(benzothiazol-2-yl)disulfide, DBTD, Di-2-benzothiazolyl disulfide, Dibenzothiazolyl disulfide, Dibenzothiazyl disulfide, Dibenzothiophene disulfide, Dibenzthiazyl disulfide, Altax, Benzothiazol-2-yl disulfide, Benzothiazole disulfide, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(benzothiazolyl) disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Dibenzothiazolyl disulfide, Ekagom GS, MBTS, MBTS Rubber Accelerator, Pneumax DM, Royal MBTS, Thiofide, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, 2-Benzothiazolyl disulfide, 2-Mercaptobenzothiazole disulfide, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dithiobis[benzothiazole], Accel TM, Di-2-benzothiazolyl disulfide, Dibenzoylthiazyl disulfide, 2-Mercaptobenzothiazyl disulfide, Dibenzothiazolyl disulphide, Dwusiarczek dwubenzotiazylu, USAF CY-5, USAF EK-5432, Vulkacit DM/MGC, Dibenzothiazole disulfide, Dibenzthiazyl disulfide, Mercaptobenzthiazyl ether, Naugex MBT, Perkacit MBTS, 2-Benzothiazyl disulfide, Dibenzothiazyl disulfide, Sanceler DM, di(benzothiazol-2-yl) disulphide, MBTS, 2,2'-Benzothiazyl disulfide, 2,2'-Bis(benzothiazolyl) disulfide, 2,2'-Dibenzothiazyldisulfide, 2,2'-Dithiobis(benzothiazole), 2-Benzothiazolyl disulfide, 2-Benzothiazyl disulfide, 2-Mercaptobenzothiazole disulfide, 2-Mercaptobenzothiazyl disulfide, Accel TM, Altax, Benzothiazole disulfide, Benzothiazole, 2,2'-dithiobis-, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Bis(benzothiazolyl) disulfide, Di-2-benzothiazolyl disulfide, Dibenzothiazolyl disulfide, Dibenzothiazolyl disulphide, Dibenzothiazyl disulfide, Dibenzoylthiazyl disulfide, Dibenzthiazyl disulfide, Dithiobis(benzothiazole), Dwusiarczek dwubenzotiazylu [Polish], Ekagom GS, MBTS, MBTS rubber accelerator, Mercaptobenzthiazyl ether, Pneumax DM, Royal MBTS, Thiofide, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, Vulkacit DM/MGC, [ChemIDplus] MBTS, [Marks, p. 98-9], Benzothiazyl disulfide, Altax, Dibenzothiazyl disulfide, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazyl disulfide, MBTS, Mercaptobenzthiazyl ether, Naugex MBT, Thiofide, Vulkacit DM, Benzothiazole disulfide, benzothiazolyl disulfide, 2-benzothiazolyl disulfide, bis(benzothiazolyl) disulfide, bis(2-benzothiazyl) disulfide, dibenzoylthiazyl disulfide, mbts rubber accelerator, 2-mercaptobenzothiazole disulfide, 2-mercaptobenzothiazyl disulfide, royal mbts, Accel TM, Benzothiazol-2-yl disulfide, Bis(2-benzothiazolyl) disulfide, Dithiobis(benzothiazole), Ekagom GS, Mercaptobenzothiazole disulfide, Mercaptobenzothiazyl disulfide, Pneumax DM, Vulcafor MBTS, Vulkacit DM/C, di(benzothiazol-2-yl) disulfide, 2,2'-Dibenzothiazoyl disulfide, MBTS, Accelerator, 1,2-bis(benzo[d]thiazol-2-yl)disulfane, DIBENZOTHIAZOLE DISULFIDE, benzothiazolyl, BENZOTHIAZYL DISULFIDE, 2-BENZOTHIAZOLYL DISULFIDE, Dibenzothiazolyl disulphide, di(benzothiazol-2-yl) disulphide, 2-Mercaptobenzothiazole disulfide, altax, thiofide, dibenzothiazyl disulfide, benzothiazyl disulfide, 2,2'-dithiobis benzothiazole, 2,2'-dithiobisbenzothiazole, benzothiazole disulfide, mbts, pneumax dm, vulcafor mbts, W-200947, Z56754489, F0900-0449, 2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole #, 2,2'-Benzothiazyl disulfide, 2,2'-Bis(benzothiazolyl) disulfide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dibenzothiazyldisulfide, 2,2'-Dithiobis(benzothiazole), 2-Benzothiazolyl disulfide, 2-Benzothiazyl disulfide, 2-Mercaptobenzothiazole disulfide, 2-Mercaptobenzothiazyl disulfide, 4-27-00-01862 (Beilstein Handbook Reference), AI3-07662, Accel TM, Altax, BRN 0285796, Benzothiazole disulfide, Benzothiazole, 2,2'-dithiobis-, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Bis(benzothiazolyl) disulfide, CCRIS 4637, Caswell No. 408A, Di-2-benzothiazolyl disulfide, Dibenzothiazolyl disulfide, Dibenzothiazolyl disulphide, Dibenzothiazyl disulfide, Dibenzoylthiazyl disulfide, Dibenzthiazyl disulfide, Dithiobis(benzothiazole), Dwusiarczek dwubenzotiazylu, Dwusiarczek dwubenzotiazylu [Polish], EINECS 204-424-9, EPA Pesticide Chemical Code 009202, Ekagom GS, HSDB 1137, MBTS, MBTS rubber accelerator, Mercaptobenzthiazyl ether, NSC 2, Pneumax DM, Royal MBTS, Thiofide, USAF CY-5, USAF EK-5432, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, Vulkacit DM/mgc, Altax, Benzothiazol-2-yl disulfide, Benzothiazole disulfide, Benzothiazolyl disulfide, Benzothiazyl disulfide, Bis(benzothiazolyl) disulfide, Bis(2-benzothiazolyl) disulfide, Bis(2-benzothiazyl) disulfide, Dibenzothiazolyl disulfide, Ekagom GS, MBTS, MBTS Rubber Accelerator, Pneumax DM, Royal MBTS, Thiofide, Vulcafor MBTS, Vulkacit DM, Vulkacit DM/C, 2-Benzothiazolyl disulfide, 2-Mercaptobenzothiazole disulfide, 2,2'-Benzothiazyl disulfide, 2,2'-Dibenzothiazyl disulfide, 2,2'-Dithiobis[benzothiazole], Accel TM, Di-2-benzothiazolyl disulfide, Dibenzoylthiazyl disulfide, 2-Mercaptobenzothiazyl disulfide, Dibenzothiazolyl disulphide, Dwusiarczek dwubenzotiazylu, USAF CY-5, USAF EK-5432, Vulkacit DM/MGC, Dibenzothiazole disulfide, Dibenzthiazyl disulfide, Mercaptobenzthiazyl ether, Naugex MBT, Perkacit MBTS, 2-Benzothiazyl disulfide, Dibenzothiazyl disulfide, Sanceler DM, di(benzothiazol-2-yl) disulphide, DM, MBTS, acceltm, Accel TM, AcceleratorDM, Acelerator DM, benzothiazolyl, AcceleratorMBTS, accelerator(dm), Accelerator (DM), Accelerator MBTS, Benzothiazyldisuflide, Rubber Accelerator DM, benzothiazoledisulfide, Rubber Accelerator MBTS, Benzothiazole disulfide, 2-benzothiazyldisulfide, Dibenzothiazole Disulfide, 2,2'-dithiobis-benzothiazol, Benzothiazol-2-yl disulfide, 2,2'-Dithiobis(Benzothiazole), 2,2'-Dibenzothiazoledisulfide, 2,2-D ibenzothiazole Disulfide, 2,2'-Dibenzothiazole disulfide, Benzothiazole, 2,2'-dithiobis-, 2-mercaptobenzothiazyldisulfide, 1,3-benzothiazole 1,1-disulfide, 2-mercaptobenzothiazoledisulfide, 2-Mercaptobenzothiazyl disulfide, 2,2'-bis(benzothiazolyl)disulfide, 2-Mercaptobenzothiazole disulfide, 2,2'-disulfanediylbis(1,3-benzothiazole), Rubber Pharmaceutical intermediate Refined(DM), 2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole

2,2'-Dibenzothiazyl disulfide (MBTS) is an organic compound.
At room temperature, 2,2'-Dibenzothiazyl disulfide (MBTS) appears as a yellowish crystalline solid with no significant odor.
2,2'-Dibenzothiazyl disulfide (MBTS) belongs to the class of aromatic heterocyclic compounds due to its benzothiazole moieties, which are fused-ring systems containing both sulfur and nitrogen atoms.

Additionally, 2,2'-Dibenzothiazyl disulfide (MBTS) can be classified as a thioether derivative because of the disulfide linkage (-S-S-) connecting the two benzothiazole rings.
This structural characteristic contributes to 2,2'-Dibenzothiazyl disulfide (MBTS)'s unique chemical properties and reactivity profile.
The synthesis of 2,2'-Dibenzothiazyl disulfide (MBTS) dates back to early studies in organic chemistry, where chemists sought to explore the reactivity of sulfur-containing aromatic systems.

Although specific details about its discoverer or exact year of synthesis may not always be well-documented, methods for producing this compound typically involve the oxidation of benzothiazole derivatives under controlled conditions.
For example, one common approach involves reacting benzothiazole with an oxidizing agent such as iodine or hydrogen peroxide in the presence of a suitable solvent.

Industrially, 2,2'-Dibenzothiazyl disulfide (MBTS) finds extensive application in the rubber industry as an accelerator for vulcanization processes, enhancing the cross-linking efficiency between polymer chains.
Beyond rubber manufacturing, 2,2'-Dibenzothiazyl disulfide (MBTS) also serves as a building block in pharmaceuticals and agrochemicals, where its ability to participate in redox reactions makes it valuable for synthesizing more complex molecules.

Despite being primarily synthetic, related compounds might occur naturally in certain microbial metabolites; however, pure 2,2'-Dibenzothiazyl disulfide (MBTS) itself does not have known natural sources.
2,2'-Dibenzothiazyl disulfide (MBTS)'s industrial preparation usually begins with commercially available benzothiazole, which undergoes oxidative coupling reactions at elevated temperatures under acidic conditions to form the desired product.

2,2'-Dibenzothiazyl disulfide (MBTS) is a chemical compound from the group of thiazoles .
2,2'-Dibenzothiazyl disulfide (MBTS) can be obtained by oxidation of 2-mercaptobenzothiazole .
2,2'-Dibenzothiazyl disulfide (MBTS) is a difficult-to-ignite, crystalline, yellowish solid with an unpleasant odor that is practically insoluble in water.

2,2'-Dibenzothiazyl disulfide (MBTS) decomposes upon heating.
2,2'-Dibenzothiazyl disulfide (MBTS) is a non-staining, primary thiazole accelerator widely used in both natural and synthetic rubber compounds.
2,2'-Dibenzothiazyl disulfide (MBTS) exhibits high activity at temperatures above 280°F.

For effective curing, 2,2'-Dibenzothiazyl disulfide (MBTS) requires activation with zinc oxide, a fatty acid, and sulfur.
When used alongside secondary accelerators such as aldehyde amines, dithiocarbamates, guanidines, or thiurams, 2,2'-Dibenzothiazyl disulfide (MBTS) can significantly enhance cure rates.
In addition to its role as an accelerator, 2,2'-Dibenzothiazyl disulfide (MBTS) also functions as a retarder in polychloroprene and peroxide cure systems, helping to control scorch and processing safety.

2,2'-Dibenzothiazyl disulfide (MBTS) is a rubber chemical used as a vulcanization accelerant.
The most frequent occupational categories are metal industry, homemakers, health services and laboratories, and building industries.
2,2'-Dibenzothiazyl disulfide (MBTS) is a yellow amorphous powder

2,2'-Dibenzothiazyl disulfide (MBTS) has the potential to combat HPV, acting as a zinc-ejecting inhibitor.
2,2'-Dibenzothiazyl disulfide (MBTS) also can act as radical polymerization photo-initiators or co-initiators.
2,2'-Dibenzothiazyl disulfide (MBTS) is an accelerator for natural rubber, nitrile-butadiene, butyl and styrene-butadiene rubber; a retarder for chloroprene rubber.

2,2'-Dibenzothiazyl disulfide (MBTS) is an organic disulfide resulting from the formal oxidative coupling of the thiol groups of two molecules of 1,3-benzothiazole-2-thiol.
2,2'-Dibenzothiazyl disulfide (MBTS) is a cream to light yellow powder.
2,2'-Dibenzothiazyl disulfide (MBTS) is insoluble in water.

2,2'-Dibenzothiazyl disulfide (MBTS) is incompatible with strong oxidizers.
2,2'-Dibenzothiazyl disulfide (MBTS) is a component of mercapto mix.
Dibenzothiazole disulfide, also known as 2,2'-Dibenzothiazyl disulfide (MBTS), is a chemical compound primarily used as a vulcanization accelerator in the rubber industry.

2,2'-Dibenzothiazyl disulfide (MBTS) is a pale yellow to off-white solid and is formed by the coupling of 2-mercaptobenzothiazole (MBT) with an oxidant.
2,2'-Dibenzothiazyl disulfide (MBTS) is an odorless, pale yellow to gray powder widely used as a vulcanization accelerator in natural and synthetic rubber processing,
2,2'-Dibenzothiazyl disulfide (MBTS) is an accelerator for rubber processing and PVC.

2,2'-Dibenzothiazyl disulfide (MBTS) is found in the rubber industry.
2,2'-Dibenzothiazyl disulfide (MBTS) is a cream to light yellow powder.
2,2'-Dibenzothiazyl disulfide (MBTS) is a cream to light yellow powder.

2,2'-Dibenzothiazyl disulfide (MBTS) is an organic disulfide resulting from the formal oxidative coupling of the thiol groups of two molecules of 1,3-benzothiazole-2-thiol.
2,2'-Dibenzothiazyl disulfide (MBTS) has a role as an allergen.
2,2'-Dibenzothiazyl disulfide (MBTS) is an organic disulfide and a member of benzothiazoles.

2,2'-Dibenzothiazyl disulfide (MBTS) derives from a 1,3-benzothiazole-2-thiol.
2,2'-Dibenzothiazyl disulfide (MBTS) is an accelerator used in the processing process for natural and synthetic rubber and plastic regeneration.
2,2'-Dibenzothiazyl disulfide (MBTS) belongs to the class of organic compounds known as benzothiazoles.

These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
2,2'-Dibenzothiazyl disulfide (MBTS) is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives.
Technically, 2,2'-Dibenzothiazyl disulfide (MBTS) is part of the human exposome.

The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health.
An individual's exposure begins before birth and includes insults from environmental and occupational sources.
2,2'-Dibenzothiazyl disulfide (MBTS) is a chemical compound that functions as an accelerator in the vulcanization of rubber.

2,2'-Dibenzothiazyl disulfide (MBTS) acts as a sulfur donor during the cross-linking process, promoting the formation of strong and durable rubber products.
2,2'-Dibenzothiazyl disulfide (MBTS) works by reacting with the rubber polymer chains, leading to the formation of cross-links between the chains.
These cross-links enhance the mechanical properties of 2,2'-Dibenzothiazyl disulfide (MBTS) such as its strength, elasticity, and resistance to heat and aging.

In experimental applications, 2,2'-Dibenzothiazyl disulfide (MBTS) may play a role in the modification of rubber properties, contributing to the development of high-performance rubber materials for various industrial applications.
2,2'-Dibenzothiazyl disulfide (MBTS)'s mode of action involves facilitating the cross-linking process, ultimately leading to the enhancement of rubber′s mechanical and thermal properties.

2,2'-Dibenzothiazyl disulfide (MBTS) is an organosulfur compound widely used as a primary accelerator in the vulcanization of natural rubber and synthetic elastomers.
2,2'-Dibenzothiazyl disulfide (MBTS) belongs to the benzothiazole class of rubber chemicals and has been one of the most important sulfur vulcanization accelerators for decades.

2,2'-Dibenzothiazyl disulfide (MBTS) provides a balanced cure rate while offering excellent processing safety, making it particularly valuable in manufacturing rubber products that require consistent mechanical properties and good aging resistance.
2,2'-Dibenzothiazyl disulfide (MBTS) is frequently employed either alone or in combination with secondary accelerators to optimize curing performance and improve the overall quality of vulcanized rubber.

2,2’-Dibenzothiazyl disulfide (MBTS) is a widely used sulfur vulcanization accelerator belonging to the benzothiazole family of rubber chemicals.
2,2’-Dibenzothiazyl disulfide (MBTS) is produced through the controlled oxidation of 2-mercaptobenzothiazole (MBT) and serves as a delayed-action, medium-fast primary accelerator for natural rubber and a wide variety of synthetic elastomers.

2,2’-Dibenzothiazyl disulfide (MBTS) accelerator for rubber is a general purpose accelerator for sulfur cures.
2,2’-Dibenzothiazyl disulfide (MBTS) is very active above 142°C (287°F).
2,2’-Dibenzothiazyl disulfide (MBTS) does not split off active sulfur during vulcanization.

2,2’-Dibenzothiazyl disulfide (MBTS) has a higher critical temperature than MBT, preventing early-cure and scorching.
2,2’-Dibenzothiazyl disulfide (MBTS) is an effective copper or copper alloy corrosion inhibitor.
When the cooling system contains copper equipment and raw water contains a certain amount of copper ions, 2,2’-Dibenzothiazyl disulfide (MBTS) can be added to prevent copper corrosion.

2,2’-Dibenzothiazyl disulfide (MBTS) is also an intermediate of the herbicide benzothiachlor.
2,2’-Dibenzothiazyl disulfide (MBTS) is a semi-ultra-fast rubber vulcanization accelerator used in natural and synthetic rubbers (NR, SBR, NBR, IIR, CR) to improve strength, elasticity, and aging properties.

2,2’-Dibenzothiazyl disulfide (MBTS) is an industrial chemical compound primarily used as a vulcanization accelerator in the processing of natural and synthetic rubber.
2,2’-Dibenzothiazyl disulfide (MBTS) appears as a pale yellow to gray powder and is critical for manufacturing durable rubber goods.

USES and APPLICATIONS of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
2,2'-Dibenzothiazyl disulfide (MBTS) is primarily used as a vulcanization accelerator in the rubber industry, where it promotes efficient sulfur crosslinking between polymer chains.
The resulting vulcanized rubber, 2,2'-Dibenzothiazyl disulfide (MBTS), exhibits enhanced elasticity, mechanical strength, abrasion resistance, resilience, and thermal stability.

2,2'-Dibenzothiazyl disulfide (MBTS) is extensively used in the production of automobile tires, truck tires, conveyor belts, industrial belts, rubber hoses, seals, gaskets, O-rings, vibration dampers, rubber rollers, cable insulation, footwear, molded rubber goods, rubber sheets, sporting goods, and numerous industrial rubber components.
2,2'-Dibenzothiazyl disulfide (MBTS) is also employed in latex products and technical rubber articles requiring reliable curing performance.
Beyond conventional rubber manufacturing, 2,2'-Dibenzothiazyl disulfide (MBTS) serves as an intermediate in specialty chemical production and may be incorporated into adhesive formulations, friction materials, and certain polymer processing systems where sulfur chemistry is involved.

Its controlled curing characteristics make 2,2'-Dibenzothiazyl disulfide (MBTS) particularly useful for thick rubber articles and products requiring uniform crosslink density throughout the material.
2,2'-Dibenzothiazyl disulfide (MBTS) finds various applications in different industries.
One of 2,2'-Dibenzothiazyl disulfide (MBTS)'s primary uses is as a rubber accelerator in the production of vulcanized rubber products.

2,2'-Dibenzothiazyl disulfide (MBTS) enhances the curing process by promoting crosslinking between rubber molecules, resulting in improved strength, elasticity, and durability of rubber materials.
2,2'-Dibenzothiazyl disulfide (MBTS) is commonly employed in the manufacturing of automotive tires, conveyor belts, shoe soles, and other rubber goods.
In addition to its role in rubber production, 2,2'-Dibenzothiazyl disulfide (MBTS) is utilized as a corrosion inhibitor in metalworking fluids and lubricants.

2,2'-Dibenzothiazyl disulfide (MBTS) provides protection against corrosion by forming a protective film on metal surfaces, preventing oxidation and degradation.
This application is particularly important in industries such as automotive, aerospace, and machinery, where metal components are exposed to harsh environments or corrosive substances.
Moreover, 2,2'-Dibenzothiazyl disulfide (MBTS) is employed as a chemical intermediate in the synthesis of various organic compounds.

2,2'-Dibenzothiazyl disulfide (MBTS) serves as a building block for the production of dyes, pharmaceuticals, and agrochemicals, contributing to the development of these industries.
Overall, 2,2'-Dibenzothiazyl disulfide (MBTS) plays a critical role in the rubber industry, acts as a corrosion inhibitor, and serves as a versatile chemical intermediate in different sectors, supporting advancements in technology, infrastructure, and various other applications.

2,2'-Dibenzothiazyl disulfide (MBTS) is used as a vulcanization accelerator for rubber .
2,2'-Dibenzothiazyl disulfide (MBTS) is a versatile compound with various properties and applications.
2,2'-Dibenzothiazyl disulfide (MBTS) has excellent solubility in rubber polymers, ensuring uniform distribution and enhancing performance.

2,2'-Dibenzothiazyl disulfide (MBTS) offers heat resistance and aging stability, maintaining rubber properties over time.
Uses of 2,2'-Dibenzothiazyl disulfide (MBTS): Accelerator for: Butyl and styrene-butadiene rubber, Natural rubber, Nitrile-butadiene.
2,2'-Dibenzothiazyl disulfide (MBTS) is used retarder for: Chloroprene rubber, Adhesives and cements, Antifreeze, Condoms and diaphragms, Cutting oils, Detergents, Disinfectants, repellents, fungicides, and insecticides used in agriculture, Gloves (household, work, or hospital gloves), Greases, Leather shoes (insoles, adhesives, linings),

Medical devices, Photographic film emulsion, Renal dialysis equipment.
2,2'-Dibenzothiazyl disulfide (MBTS) is used rubber in elasticized undergarments and clothing, Rubber pillows and sheets, Rubber shoes (sneakers, tennis shoes, etc), Soaps and shampoos, Sponge makeup applicators and rubber eyelash curiers, Swimwear, Tires and toys, Veterinarian products like tick and flea powders and sprays.

2,2'-Dibenzothiazyl disulfide (MBTS) is used semi ultra fast accelerator primary accelerator in vulcanization of NR, SBR, BR, NBR and others for manufacture of Tyres, Tubes, Conveyor belts, Footwear and other molded rubber products.
2,2'-Dibenzothiazyl disulfide (MBTS) is used as an accelerator in the rubber industry.

2,2'-Dibenzothiazyl disulfide (MBTS) is added to many types of rubber before vulcanization.
Additionally, 2,2'-Dibenzothiazyl disulfide (MBTS) is non-staining and non-discoloring, making it suitable for light-colored rubber products.
2,2'-Dibenzothiazyl disulfide (MBTS) can be used as accelerator for general rubber.

2,2'-Dibenzothiazyl disulfide (MBTS) is also used as plasticizer in chloroprene rubbes1.
2,2'-Dibenzothiazyl disulfide (MBTS)'s industry uses also include fillers, fuels and fuel additives, intermediates, process regulator, propels and blowing agents.
2,2'-Dibenzothiazyl disulfide (MBTS) is widely used as a rubber accelerator in tire manufacturing, conveyor belts, and shoe soles.

2,2'-Dibenzothiazyl disulfide (MBTS) also serves as a corrosion inhibitor in metalworking fluids and lubricants.
Moreover, 2,2'-Dibenzothiazyl disulfide (MBTS) is a chemical intermediate in the production of dyes, pharmaceuticals, and agrochemicals.
2,2'-Dibenzothiazyl disulfide (MBTS) is a valuable compound in the rubber industry and other sectors.

2,2'-Dibenzothiazyl disulfide (MBTS) is a universal accelerator for natural rubber, synthetic rubber, and reclaimed rubber.
2,2'-Dibenzothiazyl disulfide (MBTS) is easy to disperse and does not pollute in the rubber compound.
Vulcanized rubber has excellent aging resistance, but items that come into contact with vulcanized rubber tend to have a bitter taste, so 2,2'-Dibenzothiazyl disulfide (MBTS) is not suitable for rubber products that come into contact with food.

2,2'-Dibenzothiazyl disulfide (MBTS) can be used to manufacture tires, hoses, tapes, tapes, general industrial rubber products, etc.
2,2'-Dibenzothiazyl disulfide (MBTS) is usually combined with thiurams, dithiocarbamates, silica gel, guanidine accelerators to increase activity.
2,2'-Dibenzothiazyl disulfide (MBTS) needs to be mixed with zinc oxide and stearic acid.
2,2'-Dibenzothiazyl disulfide (MBTS) is used as an accelerator in the rubber industry.

2,2’-Dibenzothiazyl disulfide (MBTS) is commonly used alone or together with secondary accelerators such as thiurams, dithiocarbamates, guanidines, and sulfenamides to optimize cure rate, crosslink density, and physical properties.
2,2’-Dibenzothiazyl disulfide (MBTS) is used retarder for chloroprene rubber.
2,2’-Dibenzothiazyl disulfide (MBTS) is primarily used as a primary sulfur vulcanization accelerator in the manufacture of natural rubber and synthetic rubber products.

2,2’-Dibenzothiazyl disulfide (MBTS) has been extensively used in the rubber industry for many decades because it provides an excellent balance between processing safety, curing efficiency, and final mechanical performance.
2,2’-Dibenzothiazyl disulfide (MBTS) is used for use in natural and synthetic rubber processing.

Compared with MBT, 2,2’-Dibenzothiazyl disulfide (MBTS) offers improved scorch safety and a slower onset of vulcanization, making it particularly suitable for complex rubber processing operations requiring extended mixing, extrusion, or molding times.
2,2’-Dibenzothiazyl disulfide (MBTS) is commonly used alone or together with secondary accelerators such as thiurams, dithiocarbamates, guanidines, and sulfenamides to optimize cure rate, crosslink density, and physical properties.

2,2’-Dibenzothiazyl disulfide (MBTS) offers higher scorch safety than MBT, making it ideal for tires, hoses, seals, conveyor belts, and technical rubber goods, typically used at levels below 3.0 phr.
Uses of 2,2’-Dibenzothiazyl disulfide (MBTS): Accelerator for natural rubber, nitrile-butadiene, butyl and styrene-butadiene rubber.
2,2’-Dibenzothiazyl disulfide (MBTS) is used retarder for chloroprene rubber.

2,2’-Dibenzothiazyl disulfide (MBTS) is primarily used as a primary sulfur vulcanization accelerator in the manufacture of natural rubber and synthetic rubber products.
2,2’-Dibenzothiazyl disulfide (MBTS) is extensively employed in the production of passenger car tires, truck tires, aircraft tires, conveyor belts, transmission belts, industrial hoses, seals, gaskets, O-rings, cable insulation, vibration mounts, anti-vibration components, rubber rollers, footwear, molded rubber goods, rubber sheets, and various mechanical rubber products.

Its delayed curing characteristics make 2,2’-Dibenzothiazyl disulfide (MBTS) particularly suitable for complex molded articles, thick-section rubber products, and manufacturing processes requiring long mixing or shaping times before vulcanization.
2,2’-Dibenzothiazyl disulfide (MBTS) is also widely used in latex compounds and technical rubber goods where balanced curing characteristics are essential.
Outside conventional rubber manufacturing, 2,2’-Dibenzothiazyl disulfide (MBTS) serves as an intermediate in specialty chemical synthesis and is occasionally used in the production of lubricant additives, corrosion inhibitors, adhesive formulations, polymer processing additives, and specialty sulfur-containing chemicals.

KEY CHARACTERISTICS and USES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
Rubber Accelerator: 2,2'-Dibenzothiazyl disulfide (MBTS) is widely used to speed up the vulcanization process of both natural and synthetic rubber, leading to improved properties like elasticity and durability.
Intermediate: 2,2'-Dibenzothiazyl disulfide (MBTS) serves as an intermediate in the production of cephalosporins, an important class of antibiotics.

Other Applications: 2,2'-Dibenzothiazyl disulfide (MBTS) can also be found in plastic regeneration, polychloroprene plasticizers/retarders, and as a cure modifier for neoprene type W.
Physical Properties: 2,2'-Dibenzothiazyl disulfide (MBTS) is an organic disulfide with a melting point typically between 177-180°C.

CHARACTERISTICS of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
2,2'-Dibenzothiazyl disulfide (MBTS) is considered a medium-speed sulfur vulcanization accelerator with excellent scorch safety, allowing sufficient processing time before curing begins.
Compared with faster accelerators, 2,2'-Dibenzothiazyl disulfide (MBTS) provides more controlled vulcanization, reducing the risk of premature curing during mixing and molding operations.

2,2'-Dibenzothiazyl disulfide (MBTS) produces vulcanizates with good tensile strength, abrasion resistance, elasticity, and long-term durability.
2,2'-Dibenzothiazyl disulfide (MBTS) exhibits good compatibility with natural rubber, styrene-butadiene rubber (SBR), nitrile rubber (NBR), butadiene rubber (BR), and several other sulfur-curable elastomers.

Because of its balanced curing characteristics, 2,2'-Dibenzothiazyl disulfide (MBTS) is frequently combined with ultra-accelerators such as TMTD, ZDEC, ZDBC, or CBS to obtain faster curing while maintaining processing safety.
2,2'-Dibenzothiazyl disulfide (MBTS) is relatively stable during storage and possesses low volatility, minimizing evaporative losses during industrial processing.
Its delayed action characteristics make 2,2'-Dibenzothiazyl disulfide (MBTS) suitable for complex rubber molding operations requiring extended processing times.

2,2’-Dibenzothiazyl disulfide (MBTS) is classified as a delayed-action, medium-speed sulfur vulcanization accelerator.
2,2’-Dibenzothiazyl disulfide (MBTS)'s most important characteristic is its excellent scorch safety, which allows rubber compounds to undergo extended processing before vulcanization begins.

This minimizes premature curing during mixing, calendaring, extrusion, and molding operations.
Unlike faster accelerators such as dithiocarbamates or thiurams, 2,2’-Dibenzothiazyl disulfide (MBTS) provides a more gradual cure profile, resulting in improved processing control and uniform crosslink formation.

2,2’-Dibenzothiazyl disulfide (MBTS) is especially effective in thick rubber articles where homogeneous curing throughout the product is essential.
2,2’-Dibenzothiazyl disulfide (MBTS) demonstrates excellent compatibility with natural rubber (NR), styrene-butadiene rubber (SBR), butadiene rubber (BR), nitrile rubber (NBR), chloroprene rubber (CR), and several other sulfur-curable elastomers.

2,2’-Dibenzothiazyl disulfide (MBTS) is frequently combined with diphenylguanidine (DPG), tetramethylthiuram disulfide (TMTD), zinc dithiocarbamates, or sulfenamide
accelerators to increase cure speed while maintaining excellent scorch resistance.
2,2’-Dibenzothiazyl disulfide (MBTS) exhibits low volatility, good storage stability, and high thermal resistance under normal rubber processing conditions.
Because 2,2’-Dibenzothiazyl disulfide (MBTS) is generated by oxidation of MBT, it provides a cleaner and more controlled vulcanization process than MBT alone in many industrial formulations.

BENEFITS of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
2,2'-Dibenzothiazyl disulfide (MBTS) provides excellent processing safety by delaying the onset of vulcanization during mixing and shaping operations, thereby reducing the likelihood of scorch defects.
2,2'-Dibenzothiazyl disulfide (MBTS) produces consistent curing behavior and allows manufacturers greater flexibility during processing.

2,2'-Dibenzothiazyl disulfide (MBTS) improves tensile strength, tear resistance, resilience, fatigue resistance, and abrasion resistance of vulcanized rubber.
2,2'-Dibenzothiazyl disulfide (MBTS) contributes to longer service life and better mechanical performance of finished rubber products while maintaining dimensional stability.

Another important benefit is 2,2'-Dibenzothiazyl disulfide (MBTS)'s compatibility with numerous secondary accelerators, enabling formulators to tailor cure speed and crosslink structure according to specific application requirements.
2,2'-Dibenzothiazyl disulfide (MBTS) also exhibits relatively low volatility, reducing material losses during manufacturing and contributing to stable product quality.

2,2’-Dibenzothiazyl disulfide (MBTS) provides outstanding processing safety by delaying the onset of vulcanization, thereby reducing the risk of scorch during mixing and forming operations.
This enables manufacturers to process complex rubber compounds with greater confidence and fewer production defects.
2,2’-Dibenzothiazyl disulfide (MBTS) produces vulcanized rubber with excellent tensile strength, tear resistance, resilience, elasticity, abrasion resistance, fatigue resistance, and long-term durability.

2,2’-Dibenzothiazyl disulfide (MBTS) contributes to improved dimensional stability and consistent crosslink density throughout thick rubber products.
Another major advantage is 2,2’-Dibenzothiazyl disulfide (MBTS)'s versatility.
2,2’-Dibenzothiazyl disulfide (MBTS) performs effectively across numerous sulfur-curable elastomers and exhibits excellent compatibility with secondary accelerator systems, allowing compound formulators to tailor cure speed, crosslink structure, and physical performance according to specific application requirements.

Its relatively low volatility, excellent storage stability, and predictable curing behavior make 2,2’-Dibenzothiazyl disulfide (MBTS) one of the most reliable and widely accepted accelerators in modern rubber technology.
2,2’-Dibenzothiazyl disulfide (MBTS) also contributes to improved heat aging resistance and long service life of finished rubber components.

WHAT IS 2,2’-DİBENZOTHIAZYL DISULFIDE (MBTS) AND WHERE IS 2,2’-DIBENZOTHIAZYL DISULFIDE (MBTS) FOUND?
2,2’-Dibenzothiazyl disulfide (MBTS) is an accelerator for natural rubber, synthetic rubber and plastic regeneration.
2,2’-Dibenzothiazyl disulfide (MBTS)'s usage includes tires, hoses, rubber mats, tarpaulins, unveiled silk goods, wires, cables, and other ‘non-food’ use of rubber products.
Further research may identify additional product or industrial usages of 2,2’-Dibenzothiazyl disulfide (MBTS).

ALTERNATIVE PARENTS of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
*Benzenoids
*Thiazoles
*Heteroaromatic compounds
*Organic disulfides
*Sulfenyl compounds
*Azacyclic compounds
*Organopnictogen compounds
*Organonitrogen compounds
*Hydrocarbon derivatives

SUBSTITUENTS of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
*1,3-benzothiazole
*Benzenoid
*Heteroaromatic compound
*Thiazole
*Azole
*Organic disulfide
*Azacycle
*Sulfenyl compound
*Organic nitrogen compound
*Organopnictogen compound
*Hydrocarbon derivative
*Organosulfur compound
*Organonitrogen compound
*Aromatic heteropolycyclic compound

PROPERTIES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
2,2'-Dibenzothiazyl disulfide (MBTS) possesses several notable properties that contribute to its effectiveness in rubber applications.
Firstly, 2,2'-Dibenzothiazyl disulfide (MBTS) has excellent solubility in various rubber polymers, enabling easy incorporation into rubber compounds.
This property ensures uniform distribution throughout 2,2'-Dibenzothiazyl disulfide (MBTS), enhancing its overall performance.

Secondly, 2,2'-Dibenzothiazyl disulfide (MBTS) exhibits moderate reactivity, allowing it to promote the vulcanization process at a controlled rate.
2,2'-Dibenzothiazyl disulfide (MBTS)'s ability to facilitate the cross-linking of polymer chains enhances the mechanical strength, elasticity, and durability of rubber products.

Additionally, 2,2'-Dibenzothiazyl disulfide (MBTS) offers good heat resistance and aging stability to rubber compounds.
This property ensures that the vulcanized rubber maintains 2,2'-Dibenzothiazyl disulfide (MBTS)'s properties over an extended period, even under high-temperature conditions or exposure to environmental factors.

Furthermore, it is worth mentioning that 2,2'-Dibenzothiazyl disulfide (MBTS) is non-staining and non-discoloring, making it suitable for light-colored or white rubber products where visual aesthetics are important.
In summary, 2,2'-Dibenzothiazyl disulfide (MBTS) possesses desirable properties such as good solubility, controlled reactivity, heat resistance, and non-staining characteristics, making it a valuable accelerator in the rubber industry.

PHYSICAL and CHEMICAL PROPERTIES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
CAS Number: 120-78-5
Molecular Weight: 332.49
EC Number: 204-424-9
MDL Number: MFCD00022874
Beilstein Number: 0285796
XlogP3-AA: 5.60 (estimated)
Formula: C14 H8 N2 S4
Appearance: White powder or pellets (estimated)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 180.00 °C. @ 760.00 mm Hg
Boiling Point: 532.00 to 533.00 °C. @ 760.00 mm Hg (estimated)
Flash Point: 529.00 °F. TCC (275.80 °C.) (estimated)
logP (o/w): 5.769 (estimated)
Soluble in water, 10 mg/L @ 25 °C (experimental)
Physical State: Needles

Color: Light yellow
Odor: No data available
Melting Point/Freezing Point: 177 - 180 °C (literature value)
Initial Boiling Point and Boiling Range: No data available
Flammability (Solid, Gas): The product is not flammable.
Upper/Lower Flammability or Explosive Limits: No data available
Flash Point: No data available
Autoignition Temperature: Not auto-flammable
Decomposition Temperature: No data available
pH: No data available
Viscosity:
Kinematic Viscosity: No data available
Dynamic Viscosity: No data available
Water Solubility: 0.088 g/L at 22 °C

Partition Coefficient (n-octanol/water): Log Pow 4.5
Vapor Pressure: No data available
Density: 1.34 g/cm3
Relative Density: 1.5 at 19 °C
Relative Vapor Density: Not available
Particle Characteristics: No data available
Explosive Properties: No data available
Oxidizing Properties: None
Other Safety Information: No data available
CAS Number: 120-78-5
Molecular Formula: C14H8N2S4
SMILES: C1=CC=C2C(=C1)N=C(S2)SSC3=NC4=CC=CC=C4S3
Molecular Weight (g/mol): 332.472
ChEBI: CHEBI:53239
Percent Purity: ≥96.0% (HPLC, N)

Chemical Name or Material: 2,2′-Dibenzothiazolyl Disulfide
Melting Point: 178°C
MDL Number: MFCD00022874
UN Number: 3077
InChI Key: AFZSMODLJJCVPP-UHFFFAOYSA-N
IUPAC Name: 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole
PubChem CID: 8447
Formula Weight: 332.47
Physical Form: Crystalline Powder
Molecular Formula: C14H8N2S4
Molar Mass: 332.49 g/mol
Density: 1.467 g/cm3
Melting Point: 177-180°C
Boiling Point: 358.898°C at 760 mmHg
Flash Point: 170.855°C

Water Solubility: <0.01 g/100 mL at 21°C
Vapor Pressure: 0 mmHg at 25°C
Appearance: Crystallization
Storage Condition: 2-8°C
Sensitivity: Easily absorbing moisture
Refractive Index: 1.752
MDL Number: MFCD00022874
Physical and Chemical Properties: Density 1.5, melting point 177-180°C, flash point 271°C, water-soluble <0.01g/100 mL at 21°C
CAS Number: 120-78-5
EINECS Number: 204-424-9
InChI: InChI=1/C14H8N2S4/c1-3-7-11-9(5-1)15-13(17-11)19-20-14-16-10-6-2-4-8-12(10)18-14/h1-8H
CBNumber: CB7154687
Molecular Weight: 332.49 g/mol
MDL Number: MFCD00022874
MOL File: 120-78-5.mol

Melting point: 177-180 °C (lit.)
Boiling point: 532.5±33.0 °C (Predicted)
Density: 1.5
Vapor pressure: 0 Pa at 25 °C
Refractive index: 1.5700 (estimate)
Flash point: 271 °C
Storage temperature: Keep in a dark place, sealed in dry conditions, at room temperature
Solubility: 0.01 g/L
Form: Powder to crystal
pKa: -0.58±0.10 (Predicted)
Color: Cream to pale-yellow powder

Odor: Gray-white to cream powder or pellets, slight odor
Water solubility: <0.01 g/100 mL at 21 °C
Merck Index: 14,3370
InChIKey: AFZSMODLJJCVPP-UHFFFAOYSA-N
LogP: 4.5 at 20 °C
CAS DataBase Reference: 120-78-5 (CAS DataBase Reference)
Indirect Additives used in Food Contact Substances: 2,2'-DITHIOBIS(BENZOTHIAZOLE)
FDA 21 CFR: 175.105; 177.2600
EWG's Food Scores: 2-3
FDA UNII: 6OK753033Z
NIST Chemistry Reference: Benzothiazyl disulfide (120-78-5)
EPA Substance Registry System: 2,2'-Dithiobisbenzothiazole (120-78-5)

Appearance: Pale yellow to light yellow powder or granular solid.
Odor: Slight characteristic sulfur-like odor; nearly odorless under normal conditions.
Physical State: Solid at room temperature.
Color: Light cream to pale yellow.
Molecular Weight: 332.47 g/mol.
Molecular Formula: C14H8N2S4.
Density: Approximately 1.45–1.55 g/cm³ at 20°C.
Melting Point: Approximately 165–181°C (decomposes near melting).
Boiling Point: Not applicable; decomposes before boiling.
Flash Point: Greater than 250°C.
Autoignition Temperature: Above 300°C.

Vapor Pressure: Extremely low at ambient temperature.
Vapor Density: Not applicable due to negligible volatility.
Solubility in Water: Practically insoluble.
Solubility in Organic Solvents: Slightly soluble in benzene, chloroform, carbon disulfide, acetone and aromatic hydrocarbons; soluble in certain chlorinated solvents.
Partition Coefficient (log Kow): Approximately 4.5–5.0.
pH: Not applicable (insoluble in water).
Explosive Properties: Dust may form explosive mixtures with air under certain conditions.
Oxidizing Properties: Not classified as an oxidizer.

Thermal Stability: Stable under recommended storage conditions but decomposes when heated excessively.
Hygroscopicity: Low moisture absorption.
Decomposition Products: Sulfur oxides (SOx), nitrogen oxides (NOx), carbon oxides (COx), and sulfur-containing organic compounds may be produced during thermal decomposition.
Chemical Stability: Stable under normal industrial handling and storage conditions.
Reactivity: Reacts with strong oxidizing agents and strong reducing agents; incompatible with highly reactive chemicals.

Molecular Weight: 332.48700
Exact Mass: 332.49
EC Number: 204-424-9
UNII: 6OK753033Z
ICSC Number: 0505
NSC Number: 677459
UN Number: 3077
DSSTox ID: DTXSID1020146
Color/Form: PALE YELLOW NEEDLES FROM BENZENE|FREE-FLOWING POWDER|Cream to off-white powder or pellets
HScode: 2934200090
PSA: 132.86000
XLogP3: 5.6
Appearance: yellow amorphous powder

Density: 1.50 g/cm3
Melting Point: 180 °C
Boiling Point: 532.5ºC at 760 mmHg
Flash Point: 271ºC
Refractive Index: 1.752
Water Solubility: H2O: <0.01 g/100 mL at 21 ºC
Storage Conditions: Store in a cool, dry, well-ventilated area away from incompatible substances. Keep containers tightly closed.
Vapor Pressure: 0mmHg at 25°C
Odor: ODORLESS

Air and Water Reactions: Insoluble in water.
Reactive Group: Amines, Phosphines, and Pyridines
Reactivity Profile: 2,2'-DITHIOBISBENZOTHIAZOLE is incompatible with strong oxidizers. (NTP, 1992).
Physical Dangers: Dust explosion possible if in powder or granular form, mixed with air.
Chemical Formula: C14H8N2S4
Average Molecular Weight: 332.47
Monoisotopic Molecular Weight: 331.957032962
IUPAC Name: 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole
Traditional Name: altax
CAS Registry Number: Not Available
SMILES: S(SC1=NC2=CC=CC=C2S1)C1=NC2=CC=CC=C2S1

InChI Identifier: InChI=1S/C14H8N2S4/c1-3-7-11-9(5-1)15-13(17-11)19-20-14-16-10-6-2-4-8-12(10)18-14/h1-8H
InChI Key: AFZSMODLJJCVPP-UHFFFAOYSA-N
Chemical Name: 2,2'-Dibenzothiazyl disulfide
Common Name: MBTS
CAS Number: 120-78-5
EC Number: 204-424-9
Molecular Formula: C14H8N2S4
Molecular Weight: 332.47 g/mol
CBNumber: CB7154687
Molecular Formula: C14H8N2S4
Molecular Weight: 332.49

MDL Number: MFCD00022874
MOL File: 120-78-5.mol
Melting point: 177-180 °C (lit.)
Boiling point: 532.5±33.0 °C(Predicted)
Density: 1.5
vapor pressure: 0Pa at 25℃
refractive index: 1.5700 (estimate)
Flash point: 271°C
storage temp.: Keep in dark place,Sealed in dry,Room Temperature
solubility: 0.01g/l

form: powder to crystal
pka: -0.58±0.10(Predicted)
color: Cream to pale-yellow powder
Odor: gray-wh. to cream powd. or pellets, sl. odor
Water Solubility: <0.01 g/100 mL at 21 ºC
Merck: 14,3370
Henry's Law Constant: 4.2×107 mol/(m3Pa) at 25℃
InChI: 1S/C14H8N2S4/c1-3-7-11-9(5-1)15-13(17-11)19-20-14-16-10-6-2-4-8-12(10)18-14/h1-8H
InChIKey: AFZSMODLJJCVPP-UHFFFAOYSA-N
SMILES: S(Sc1nc2ccccc2s1)c3nc4ccccc4s3
LogP: 4.5 at 20℃
CAS DataBase Reference: 120-78-5(CAS DataBase Reference)

Indirect Additives used in Food Contact Substances: 2,2'-DITHIOBIS(BENZOTHIAZOLE)
FDA 21 CFR: 175.105; 177.2600
EWG's Food Scores: 2-3
FDA UNII: 6OK753033Z
NIST Chemistry Reference: Benzothiazyl disulfide(120-78-5)
EPA Substance Registry System: 2,2'-Dithiobisbenzothiazole (120-78-5)
UNSPSC Code: 12352100
NACRES: NA.22
IUPAC Name: Dibenzothiazyl Disulfide
Abbreviation: MBTS

Product Name: Dibenzothiazyl Disulfide
Synonyms: 2,2’-Benzothiazyl Ddisulfide , MBTS; Dithiobis
Chemical Formula: C14H8N2S4
Molecular Weight: 332.47
CAS: 120-78-5
EC No: 204-424-9
Density: 1.54 g/cm3 at 25°C
Melting Range: 170°C- 179°C
CAS Number: 120-78-5
Molecular Formula: C₁₄H₈N₂S₄
Molecular Weight: 332.49

Purity: ≥95%
Appearance: Supplied as an off-white to yellow solid
Solubility: Chloroform, Dioxane (Sparingly), DMSO (Sparingly), Ethyl Acetate (Sparingly)
Melting Point: 175-178°C
Storage and Stability: Store at 4°C. For maximum recovery of product, centrifuge the original vial prior to removing the cap.
Molar mass: 332.47 g· mol −1
State of matter: firmly
Density: 1.34 g·cm −3
Melting point: 177–180 °C
Solubility: practically insoluble in water (40 mg·l −1 at 20 °C)

Appearance: Pale yellow to light yellow powder, granules, or free-flowing powder.
Physical State: Solid.
Color: Cream to pale yellow.
Odor: Slight characteristic sulfur odor; nearly odorless under normal conditions.
Molecular Formula: C14H8N2S4.
Molecular Weight: 332.48 g/mol.
Density: Approximately 1.45–1.54 g/cm³ at 20°C.
Melting Point: 165–181°C (decomposes near melting).
Boiling Point: Not applicable; decomposes before boiling.

Flash Point: Greater than 250°C.
Autoignition Temperature: Approximately 315–330°C.
Vapor Pressure: Extremely low (negligible at room temperature).
Volatility: Very low.
Water Solubility: Practically insoluble (typically less than 5 mg/L at 20–25°C).
Solubility in Organic Solvents: Slightly soluble in benzene, chloroform, acetone, carbon disulfide, toluene, and aromatic hydrocarbons; soluble in certain chlorinated organic solvents.
Partition Coefficient (log Kow): Approximately 4.4–5.0.
pH: Not applicable (insoluble in water).
Thermal Stability: Stable under recommended storage conditions.

Chemical Stability: Stable under normal temperatures and pressures.
Hygroscopicity: Low.
Dust Explosion Hazard: Finely divided dust may form combustible dust-air mixtures.
Oxidizing Properties: Not oxidizing.
Explosive Properties: Not classified as explosive.
Decomposition Temperature: Begins to decompose above its melting range.
Decomposition Products: Carbon monoxide (CO), carbon dioxide (CO₂), sulfur oxides (SOx), nitrogen oxides (NOx), hydrogen sulfide (H₂S), sulfur-containing organic compounds.
Reactivity: Incompatible with strong oxidizing agents, strong acids, and strong reducing agents.

Chemical Name: 2-Mercaptobenzothiazole Disulfide
Common Name: MBTS
IUPAC Name: Bis(1,3-benzothiazol-2-yl) disulfide
CAS Number: 120-78-5
EC Number: 204-424-9
Molecular Formula: C14H8N2S4
Molecular Weight: 332.48 g/mol
Molecular Weight: 332.5 g/mol
XLogP3-AA: 5.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 3
Exact Mass: 331.95703296 Da

Monoisotopic Mass: 331.95703296 Da
Topological Polar Surface Area: 133 Å²
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 311
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

FIRST AID MEASURES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available

ACCIDENTAL RELEASE MEASURES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Do not store near acids.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids

STABILITY and REACTIVITY of 2,2'-DIBENZOTHIAZYL DISULFIDE (MBTS):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available