N,N-Dimethylaniline (DMA)

CAS 121-69-7In StockSample available

Key Features

  • Fast-acting amine accelerator for BPO cobalt-free cure systems
  • Very short gel times (8–15 min at 20°C) with BPO paste
  • Enables ambient-temperature cure without cobalt compounds
  • Low viscosity for easy mixing and incorporation
  • Well-established in automotive repair and body filler applications

N,N-Dimethylaniline (DMA) is a tertiary aromatic amine accelerator used in combination with benzoyl peroxide (BPO) to achieve ambient-temperature, cobalt-free cure of unsaturated polyester and vinyl ester resins. DMA is one of the fastest-acting amine accelerators available — when combined with BPO paste, it produces very short gel times (8–15 minutes at 20°C with standard dosages), making it suitable for fast-cure applications. The mechanism involves electron transfer from DMA's amine nitrogen to BPO, generating benzoyloxy and phenyl radicals that initiate free-radical polymerization. DMA provides slightly faster acceleration than DMPT but can contribute more yellow discoloration to cured laminates and gelcoats due to oxidation of the aniline ring. Typical dosage is 0.5–2% DMA combined with 2–4% BPO paste (50%), providing gel times from 5 to 25 minutes at 20°C. DMA is a colorless to pale yellow liquid with a distinctive aromatic amine odor. It is classified as toxic (skin penetration) and a suspected carcinogen; appropriate PPE and ventilation are essential. Its use in food-contact applications is restricted.

Specifications

ParameterValue
Purity≥99%
AppearanceColorless to pale yellow liquid
Shelf Life24 months in sealed container
Flash Point63°C
Density (20°C)0.955–0.960 g/cm³
Viscosity (25°C)1–3 mPa·s

Applications

Cobalt-free fast-cure of UPR with BPO for automotive body fillersBPO/amine cure of polyester putties and repair compoundsFast gel time UPR in spray-up and hand lay-up with BPOCasting resin systems requiring cobalt-free cureIndustrial composite repair with accelerated BPO cure

FAQ

DMA (N,N-dimethylaniline) undergoes oxidation more readily than DMPT (N,N-dimethyl-p-toluidine) because the para position on DMA's ring is unsubstituted and accessible. Oxidation products (azobenzene derivatives, Schiff bases) are yellow-colored. DMPT has a methyl group at the para position, blocking this oxidative pathway and reducing yellowing. For color-sensitive gelcoat work, DMPT is always preferred over DMA.

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