Nadic Methyl Anhydride (NMA, Methyl Nadic)
Key Features
- Highest heat resistance of common liquid anhydride hardeners (Tg to 200°C)
- Bicyclic rigid structure restricts chain motion for extreme Tg
- Liquid at room temperature for pump metering despite high Tg potential
- Excellent hot-dry mechanical property retention above 150°C
- Preferred for aerospace tooling and high-temperature electrical applications
Nadic Methyl Anhydride (NMA), also called Methyl Nadic Anhydride or Methyl Nadic (MNA), is a bicyclic liquid anhydride curing agent for high-performance epoxy systems. The unique bicyclic norbornene-based structure of NMA provides the highest heat resistance of all common liquid anhydride hardeners, making it the preferred choice for applications requiring service temperatures above 150°C. NMA-cured epoxy systems achieve Tg values of 150–200°C with appropriate post-cure schedules, making them suitable for aerospace composite tooling, high-temperature electrical applications, and motor potting. The rigid bicyclic structure restricts chain motion, yielding exceptionally high Tg and excellent hot-dry mechanical retention. NMA has an anhydride equivalent weight (AEW) of approximately 178 g/eq. Its viscosity is slightly higher than MTHPA but still pump-able at room temperature. An accelerator (BDMA 1–2% or DMP-30 2–3%) is required. NMA is more expensive than MTHPA or MHHPA and is reserved for applications where the high Tg justifies the premium. Post-cure at 170–200°C for 2–4 hours is recommended to achieve maximum Tg and mechanical performance.
Specifications
| Parameter | Value |
|---|---|
| Appearance | Clear pale yellow liquid |
| Shelf Life | 12 months in sealed container |
| Density (20°C) | 1.22–1.24 g/cm³ |
| Viscosity (25°C) | 150–300 mPa·s |
| Cured Tg (with post-cure 200°C) | 170–200°C |
| Anhydride Equivalent Weight (AEW) | ~178 g/eq |
Applications
FAQ
The bicyclic norbornene framework in NMA creates a rigid bridge structure that severely restricts rotation around the main chain bonds in the cured epoxy network. This restricted mobility means more thermal energy is needed to activate segmental motion (defining Tg). The bicyclic bridge also reduces free volume in the cured polymer, further contributing to the high Tg. MTHPA and MHHPA have monocyclic rings that provide less steric restriction.
Direct Contact
💬WhatsApp +86 156 3910 0440Telegram +86 156 3910 0440✉️[email protected]Reply within 24 hours
Related Products
Methyltetrahydrophthalic Anhydride (MTHPA)
CAS 11070-44-3
Liquid at room temperature for easy pump metering in automated systems
Methylhexahydrophthalic Anhydride (MHHPA)
CAS 25550-51-0
Fully saturated ring structure for superior UV and color stability
Trimellitic Anhydride (TMA, High Performance)
CAS 552-30-7
Trifunctional anhydride for high crosslink density and Tg >200°C
Benzyl Dimethylamine (BDMA, Accelerator)
CAS 103-83-3
Powerful accelerator for anhydride and latent epoxy systems