What Is Accelerator MBTS (DM)?
Accelerator MBTS, also called DM, CAS 120-78-5, chemically 2,2′-dibenzothiazyl disulfide, is a thiazole-type rubber accelerator. It is a general-purpose accelerator with good scorch safety, used on its own or as a secondary accelerator (often with DPG) in tyres, technical rubber goods and general rubber.
Thiazole accelerators were the first widely used organic accelerators, and MBTS remains in heavy use because it is effective, versatile and forgiving. It is the disulfide counterpart of MBT: where MBT is the thiazole thiol, MBTS is the disulfide formed by joining two thiazole units through sulfur. That difference gives MBTS better scorch safety and less tendency to bloom. PolyBlueChem supplies Accelerator MBTS to a controlled specification with per-batch COA and SDS.
| CAS number | 120-78-5 |
| Chemical name | 2,2′-Dibenzothiazyl disulfide |
| Synonyms | Accelerator MBTS; DM; dibenzothiazyl disulfide; benzothiazyl disulfide; MBTS |
| Molecular formula | C14H8N2S4 |
| Molecular weight | 332.5 g/mol |
| Type | Thiazole accelerator (disulfide) |
| Appearance | White or light yellow powder |
Chemistry and Structure
MBTS consists of two benzothiazole units joined by a disulfide (-S-S-) bridge. The structure explains its behaviour:
- The benzothiazole rings are the active accelerator fragments; they accelerate sulfur vulcanisation once the disulfide opens.
- The disulfide bridge makes MBTS more stable and less reactive than MBT, giving better scorch safety and less tendency to bloom.
- The molecule contains no amine, so it does not raise the same nitrosamine concerns as amine-based accelerators.
Because it is a thiazole (not a sulfenamide), MBTS is not strongly delayed – it acts faster than the sulfenamides (CZ, TBBS, DCBS) but with more processing safety than MBT alone. It also acts partly as a sulfur donor through its disulfide group.
How MBTS Works as an Accelerator
In a sulfur cure, MBTS accelerates the formation of crosslinks between polymer chains. Its action can be summarised as:
- Thiazole activity – the benzothiazole fragment reacts with sulfur and the rubber, speeding the vulcanisation reaction.
- Disulfide/sulfur donation – the -S-S- group can participate in the crosslinking chemistry, so MBTS behaves partly as an accelerator and partly as a sulfur source.
- Activator dependence – like other accelerators, MBTS needs the zinc oxide/stearic acid activator system and, usually, elemental sulfur; it is often used with a secondary accelerator such as DPG to raise activity.
MBTS is therefore a versatile “primary” or “secondary” accelerator: it can accelerate a compound on its own, or be blended with other accelerators to adjust the cure.
How Accelerator MBTS Is Produced
MBTS is made by oxidising 2-mercaptobenzothiazole (MBT), which couples two thiazole thiols into the disulfide:
- MBT is dissolved or suspended in a suitable medium.
- An oxidising agent (for example, hydrogen peroxide, chlorine or a hypochlorite system) oxidatively couples the thiols.
- The disulfide product is filtered, washed, dried and milled to a powder.
Control targets complete coupling and low residual MBT, which would increase cure activity and reduce scorch safety. The specification therefore fixes melting point, heating loss, ash and sieve residue.
Specifications and Quality Control
Accelerator MBTS is supplied as a white or light yellow powder to the following specification:
| Parameter | Specification |
|---|---|
| Appearance | White or light yellow powder |
| Initial melting point | 165 °C min |
| Heating loss | 0.30% max |
| Ash | 0.30% max |
| Sieve residue (150 µm) | 0.1% max |
| Parameter | What it controls |
|---|---|
| Initial melting point (165 °C min) | Purity and identity; MBTS has a characteristically high melting point |
| Heating loss (0.30% max) | Moisture/volatiles; affects weighing and processing |
| Ash (0.30% max) | Inorganic residues |
| Sieve residue (150 µm, 0.1% max) | Particle size / dispersion |
A specification sheet and a per-batch certificate of analysis (COA) are available on request.
Key Properties
| Property | Behaviour | Practical value |
|---|---|---|
| Class | Thiazole (disulfide) | General-purpose acceleration |
| Scorch safety | Better than MBT | Safer processing |
| Bloom | Less than MBT | Cleaner compound surface |
| Secondary use | Works with DPG and other accelerators | Flexible cure tuning |
| Amine content | None | No amine-derived nitrosamine concern |
Applications
| Industry / product | Function |
|---|---|
| Tyres | General accelerator in tyre compounds; secondary accelerator |
| Belts and hoses | Acceleration of technical rubber goods |
| Footwear and mouldings | General rubber goods |
| Mechanical goods | Seals, gaskets, industrial rubber |
| General rubber | NR, SBR, BR, NBR and blends |
- Tyres and technical goods – MBTS is used as a primary accelerator or, more often, as a secondary accelerator alongside a sulfenamide or with DPG, to tune cure rate and properties.
- General rubber goods – an economical, versatile accelerator where the strong delay of a sulfenamide is not needed.
Accelerator MBTS vs Other Accelerators
| Accelerator | CAS | Class | Delay / speed | Typical role |
|---|---|---|---|---|
| MBT (M) | 149-30-4 | Thiazole (thiol) | Fast, lower scorch safety | General accelerator; intermediate |
| MBTS (DM) | 120-78-5 | Thiazole (disulfide) | Medium; better scorch than MBT | General / secondary accelerator |
| CZ (CBS) | 95-33-0 | Sulfenamide | Delayed | Tyres and technical goods |
| TBBS (NS) | 95-31-8 | Sulfenamide | Delayed | Tyres; the common sulfenamide |
| DPG (D) | 102-06-7 | Guanidine | Fast | Secondary accelerator / activator |
Guidance: use MBTS where a general-purpose, amine-free accelerator with good scorch safety is wanted; pair it with DPG to raise activity; choose a sulfenamide (CZ, TBBS, DCBS) when more delay and scorch safety are needed, as in tyres.
Dosage and Cure Systems
| Use | Character |
|---|---|
| Primary accelerator | MBTS alone, with sulfur and activators |
| Secondary / booster | MBTS with DPG or a sulfenamide to raise cure rate |
| Sulfur-donor role | The disulfide can contribute to crosslinking, allowing lower elemental sulfur |
Levels are set by the cure system and confirmed by rheometer and physical tests. As with any accelerator, MBTS works with zinc oxide and stearic acid activators and elemental sulfur.
Safety, Handling and Storage
- Skin sensitisation – like most rubber accelerators, MBTS is a potential skin sensitiser (H317); avoid skin contact and follow good industrial hygiene.
- Dust – avoid breathing the powder; use local extraction where large amounts are handled.
- No amine – because MBTS contains no amine, it does not carry the amine-derived nitrosamine concern of some accelerators.
- Storage – keep sealed, cool and dry, away from acids and oxidisers.
Regulatory Status
| Use | Status (as commonly cited) |
|---|---|
| Rubber (industrial) | Governed by the buyer’s specification and article requirements |
| Food-contact / potable-water rubber | Only where the specific accelerator is permitted; confirm the applicable regulation |
Packaging, Logistics and Supply
| Item | Standard options |
|---|---|
| Packaging | 25 kg PP/PE bags or fibre drums |
| Documentation | Per-batch COA and SDS |
| Incoterms | FOB and CIF |
| Storage | Sealed, cool and dry |
Price tracks the MBT feedstock and the finishing quality; buying on committed tonnage gives the best terms.
MBT and MBTS: The Thiazole Pair
MBT and MBTS are closely related, and buyers often need to know which to use. MBT is 2-mercaptobenzothiazole (the thiol); MBTS is its disulfide (two MBT units joined by sulfur).
| Comparison | MBT (M) | MBTS (DM) |
|---|---|---|
| Structure | Thiazole thiol | Thiazole disulfide |
| Cure activity | Faster, more active | More controlled |
| Scorch safety | Lower | Better |
| Bloom tendency | Higher | Lower |
| Typical role | Primary accelerator; MBT is also used in mineral flotation | Primary or secondary accelerator |
Where a faster cure and full activity are wanted, MBT is chosen; where better scorch safety and less bloom are wanted, MBTS. In many compounds the two are interchangeable in function, with the choice made on processing behaviour and cost.
Quality: Reading an MBTS Certificate of Analysis
| Parameter | What it tells you |
|---|---|
| Initial melting point (165 °C min) | Confirms a pure disulfide; residual MBT lowers it and raises activity |
| Heating loss (0.30% max) | Moisture/volatiles |
| Ash (0.30% max) | Inorganic residues |
| Sieve residue (150 µm, 0.1% max) | Dispersion; coarse material can cause cure defects |
Residual MBT is the parameter to watch: it makes the accelerator more active and less scorch-safe, so a consistent, low-MBT batch is what delivers consistent cure.
MBTS in Tyre and Technical Compounds
MBTS is used both as a primary accelerator and, more often, as a secondary accelerator that tunes the cure of a compound.
| Role | How MBTS is used |
|---|---|
| Primary accelerator | On its own with sulfur and activators, for general rubber goods |
| Secondary accelerator | With a sulfenamide (CZ/TBBS) to adjust cure rate and properties |
| With DPG | MBTS + DPG is a classic fast general-purpose system |
| Sulfur-donor contribution | The disulfide can contribute to crosslinking, allowing lower elemental sulfur |
Because MBTS is versatile and forgiving, it is a common “utility” accelerator in a rubber plant: it can be used alone where the strong delay of a sulfenamide is unnecessary, or blended to fine-tune a cure system that is close but not quite right.
Scorch Safety, Bloom and Processing
Two practical behaviours distinguish MBTS from its thiazole parent MBT.
- Scorch safety – MBTS is more stable than MBT, so it begins to cure later at processing temperature. This gives a wider processing window and reduces the risk of premature vulcanisation.
- Bloom – MBTS is less prone to migrate to the surface of the compound than MBT, so it leaves a cleaner surface and wastes less of the addition. Bloom can spoil appearance and reduce the effective protection the compound retains.
For these reasons MBTS often replaces MBT where a slightly more controlled, cleaner-running accelerator is wanted, at a modest cost premium.
Accelerator Combinations with MBTS
| System | Character | Where used |
|---|---|---|
| MBTS alone + sulfur | General-purpose cure | General rubber goods |
| MBTS + DPG | Faster, more active | Technical goods, footwear |
| MBTS + sulfenamide (CZ/TBBS) | Fine-tuned cure rate | Tyres and demanding goods |
| MBTS + thiuram (TMTD) | Low-sulfur / EV-type systems | Heat-resistant compounds |
Accelerator combinations are chosen so that the total system delivers the required scorch time, cure rate and final crosslink density. Because MBTS is a thiazole (not strongly delayed), it is usually paired with a more delayed accelerator when a long processing window is needed, or with DPG when more speed is needed.
The Amine-Free Advantage
Because MBTS contains no nitrogen in an amine form, it does not raise the same nitrosamine concerns as amine-derived accelerators (sulfenamides from secondary amines, thiurams/dithiocarbamates).
| Accelerator class | Nitrosamine potential |
|---|---|
| Sulfenamides from secondary amines | Higher concern |
| Sulfenamides from primary amines (CZ, TBBS) | Lower concern |
| Thiazoles (MBT, MBTS) | No amine-derived concern |
This makes MBTS attractive where a plant wants to reduce nitrosamine potential in the cure system while keeping a versatile, effective accelerator.
MBTS in Practice and Selection
MBTS is the “utility” thiazole accelerator: it can stand alone or blend with almost anything, and it is chosen when a plant wants a reliable, amine-free accelerator with sensible processing safety.
| Situation | Why MBTS fits |
|---|---|
| General rubber goods | Effective, versatile, economical |
| Need to boost a cure | Blends with DPG or a sulfenamide |
| Want less bloom than MBT | Lower bloom tendency |
| Want to avoid amine-derived nitrosamines | Amine-free thiazole |
In a compound, MBTS is set with the sulfur level, the zinc oxide/stearic acid activators and any co-accelerator. Where the cure must be more delayed, a sulfenamide is used; where it must be faster, DPG or a thiuram is added. Because MBTS continues the thiazole line from MBT, plants that already use MBT can often swap to MBTS to gain scorch safety and reduce bloom with minimal reformulation – confirming the cure on the rheometer and the physical properties on the cured article.
As a rule: use MBTS when you need a general-purpose, amine-free accelerator; step up to a sulfenamide when you need more delay and scorch safety; add DPG when you need more speed.
Frequently Asked Questions about Accelerator MBTS (DM)
What is Accelerator MBTS used for?
It is a thiazole accelerator for sulfur vulcanisation, used in tyres, technical rubber goods and general rubber, often as a secondary accelerator.
What is the CAS number of MBTS?
120-78-5.
Is MBTS the same as DM?
Yes – MBTS and DM are names for the same accelerator, 2,2′-dibenzothiazyl disulfide.
How does MBTS differ from MBT?
MBT is the thiazole thiol; MBTS is its disulfide. MBTS usually gives better scorch safety and less bloom than MBT.
Does MBTS contain an amine?
No – it contains no amine, so it does not carry the amine-derived nitrosamine concern of some accelerators.
Does MBTS need activators?
Yes – it works with zinc oxide and stearic acid and elemental sulfur, and is often boosted with DPG.
Is MBTS a skin sensitiser?
Yes – like most accelerators it is a potential skin sensitiser; avoid skin contact.
Related reading
- Accelerator MBTS (DM) in rubber vulcanization
- Rubber antioxidants and accelerators: selection guide
- Accelerator CZ (CBS): properties and applications
- Accelerator TBBS (NS): properties and applications
- Accelerator MBTS (DM, CAS 120-78-5) – product page
PolyBlueChem supplies Accelerator MBTS (DM, CAS 120-78-5) to a controlled specification, with per-batch COA and SDS, competitive pricing on bulk volumes and FOB/CIF delivery. Contact us with your application, tonnage and delivery port.