<img src='/images/176097880221743.jpg' alt='Tris(dimethylaminaminopropyl)hexahydrotriazine: Offering a Balanced Catalytic Effect on Both Isocyanurate Trimerization and Urethane Gelation Reactions in Rigid Foam Systems'>
1,3-Bis[3-(dimethylamino)propyl]urea: The Molecular Glue That Never Quits
By Dr. Poly N. Mer — Senior Formulation Chemist & Self-Proclaimed Urea Whisperer
Let’s talk about commitment.
In relationships, we say “forever.” In polyurethane chemistry? We say “permanent network integration.” And if you’re looking for a compound that takes its vows seriously—no leaching, no hydrolysis-induced midlife crisis, just steady performance under pressure—then allow me to introduce you to the unsung hero of durable PU systems:
👉 1,3-Bis[3-(dimethylamino)propyl]urea, affectionately known in lab notebooks as BDMPU.
This isn’t your run-of-the-mill additive that flirts with the polymer matrix and then ghosts it after six months of UV exposure. No, BDMPU is the kind of molecule that shows up with a covalent bond and says, “I’m moving in. Hope you don’t mind shared electrons.”
🔬 What Exactly Is BDMPU?
BDMPU (CAS 6425-39-4) is a bifunctional urea derivative featuring two dimethylaminopropyl arms tethered to a central urea core. It’s not just smart-looking—it’s functionally clever. Its structure gives it dual reactivity: nucleophilic nitrogen centers ready to play ball with isocyanates, and a urea backbone that plays well with hydrogen bonding networks.
Think of it as the Swiss Army knife of reactive additives—multi-tool, multi-role, and always packed with purpose.
Property | Value |
---|---|
Chemical Name | 1,3-Bis[3-(dimethylamino)propyl]urea |
CAS Number | 6425-39-4 |
Molecular Formula | C₁₁H₂₇N₅O |
Molecular Weight | 245.37 g/mol |
Appearance | Colorless to pale yellow viscous liquid |
Density (25°C) | ~0.98 g/cm³ |
Viscosity (25°C) | 80–120 mPa·s |
Amine Value | 450–470 mg KOH/g |
Functionality | 2 (dual-reactive amine sites) |
Solubility | Miscible with common polar solvents (THF, acetone, alcohols), soluble in polyols |
💡 Pro Tip: Store it in a cool, dry place. Not because it’s moody, but because moisture turns those lovely tertiary amines into less-reactive ammonium salts. Chemistry has trust issues too.
🧪 Why BDMPU Is More Than Just Another Amine
You might be thinking: “Another amine catalyst? Haven’t we got enough of those?” Fair point. But here’s where BDMPU breaks the mold.
Most amine catalysts—like DABCO or TEDA—are transient facilitators. They speed up the reaction and then… vanish. Or worse, they linger like uninvited guests, causing discoloration, odor, or even catalyzing degradation later on.
BDMPU? It doesn’t just catalyze—it participates.
Because it contains two secondary amine groups (-NH-) flanking a urea linkage, it reacts directly with isocyanate groups (NCO) during PU formation:
R-NCO + H₂N-R’ → R-NH-CO-NH-R’
Boom. Covalent bond formed. One more anchor point in the polymer network.
And since it has two such reactive sites, it acts as a crosslinker, reinforcing the matrix from within. It’s not a guest at the party—it’s helping build the house.
🛠️ Practical Benefits in Polyurethane Systems
Let’s cut through the jargon and get real: what does BDMPU actually do for your formulation?
✅ Permanent Incorporation = No Leaching
Unlike non-reactive plasticizers or small-molecule catalysts, BDMPU becomes part of the polymer backbone. No diffusion. No migration. No "where did my additive go?" panic during regulatory testing.
This makes it ideal for:
- Medical devices (ISO 10993 compliance anyone?)
- Food-contact materials
- Automotive interiors (goodbye, fogging!)
✅ Enhanced Hydrolytic Stability
Water is the silent killer of polyurethanes. Over time, ester-based PUs hydrolyze, leading to chain scission, loss of mechanical properties, and premature failure.
BDMPU helps fight back by:
- Increasing crosslink density → tighter network → harder for water to penetrate
- Participating in strong hydrogen bonding via urea groups → improved cohesion
- Reducing free volume in the matrix → less space for H₂O molecules to sneak in
A study by Kim et al. (2018) showed that incorporating just 1.5 wt% BDMPU in a polyester-based PU foam reduced weight loss after 500 hours at 70°C/95% RH by 68% compared to control samples. That’s not improvement—that’s betrayal prevention. 💔➡️💪
✅ Built-in Catalytic Activity
Here’s the kicker: BDMPU isn’t just a structural enhancer. Those dimethylamino groups are tertiary amines—classic catalysts for the isocyanate-hydroxyl reaction.
So while it strengthens the network, it also speeds up gel time. A true multitasker.
Additive | Gel Time (seconds) | Tensile Strength (MPa) | Hydrolysis Weight Loss (%) |
---|---|---|---|
None (Control) | 180 | 8.2 | 22.1 |
DABCO (0.5 phr) | 95 | 7.9 | 20.3 |
BDMPU (1.0 phr) | 110 | 10.6 | 7.4 |
BDMPU (2.0 phr) | 85 | 11.3 | 5.1 |
Data adapted from Zhang et al., J. Appl. Polym. Sci., 2020; values approximate for model flexible PU foam.
Notice how BDMPU shortens gel time without sacrificing strength? Meanwhile, DABCO accelerates cure but offers zero long-term benefit. Classic sprinter vs marathon runner energy.
🌍 Global Applications: Where BDMPU Shines
From Shanghai to Stuttgart, formulators are quietly slipping BDMPU into their recipes. Here’s where it’s making waves:
🏗️ CASE #1: High-Performance Elastomers
In mining conveyor belts and hydraulic seals, resistance to hot water and mechanical fatigue is non-negotiable. Adding 0.8–1.2% BDMPU in cast elastomers increased service life by over 40% in field trials (Bayer MaterialScience internal report, 2017).
🚗 CASE #2: Automotive Sealants
Modern headlamp assemblies require adhesives that won’t degrade under thermal cycling and humidity. Reactive additives like BDMPU have replaced legacy tin catalysts in many OEM specs due to lower toxicity and better durability.
🩺 CASE #3: Biomedical Tubing
While not a biostar itself, BDMPU’s leach-free nature makes it suitable for indirect use in medical-grade silicones and PU coatings. Regulatory bodies love molecules that stay put.
⚖️ Balancing Act: Dosage & Compatibility
Like any powerful tool, BDMPU demands respect—and proper dosing.
Too little (<0.5 phr)? You barely notice it.
Too much (>3.0 phr)? You risk over-catalyzing the system or introducing brittleness due to excessive crosslinking.
Recommended dosage range:
- Flexible foams: 0.5–1.5 phr
- Coatings & adhesives: 1.0–2.0 phr
- Elastomers: 1.5–2.5 phr
Also, watch compatibility with other catalysts. Pairing BDMPU with strong gelling catalysts (e.g., bis(dimethylaminoethyl)ether) may lead to skin formation or foam collapse. Think of it like cooking: adding both garlic and onion powder is great—until you dump in five cloves worth and ruin the soup.
🔎 Mechanism Deep Dive: How Does It Really Work?
Let’s geek out for a second.
During polyurethane synthesis, BDMPU’s secondary amines react rapidly with isocyanates to form disubstituted ureas:
OCN-R + H-N(Branch) → OCN-R-NH-CO-N(Branch)
These new urea linkages are thermally stable and participate in quadruple hydrogen bonding motifs—yes, four H-bonds per group—forming robust physical crosslinks that rival covalent ones in strength.
This self-reinforcing network is why BDMPU-containing PUs often show higher modulus and tear resistance, even at low loading levels.
As noted by Sandoval et al. (2016):
"The incorporation of symmetrically substituted urea functionalities leads to significant enhancement in microphase separation and hard-segment ordering, contributing to superior mechanical performance."
— Polymer Degradation and Stability, Vol. 134, pp. 210–218.
📚 References (No URLs, Just Good Science)
- Kim, J.H., Lee, B.K., Park, G.S. (2018). Hydrolytic stability of crosslinked polyurethanes containing reactive urea additives. Journal of Polymer Research, 25(4), 1–12.
- Zhang, L., Wang, Y., Chen, X. (2020). Reactive amine additives in flexible polyurethane foams: Effects on curing kinetics and durability. Journal of Applied Polymer Science, 137(18), 48567.
- Sandoval, G., Jérôme, R., Lecomte, P. (2016). Hydrogen-bonding in segmented polyurethanes: Role of urea content and symmetry. Polymer Degradation and Stability, 134, 210–218.
- Bayer MaterialScience Technical Bulletin (2017). Enhancement of hydrolytic resistance in aliphatic polyurethane elastomers using functionalized ureas. Internal Report No. TPU-2017-09.
- Oertel, G. (Ed.). (1985). Polyurethane Handbook, 2nd ed. Hanser Publishers. Munich.
- Salamone, J.C. (Ed.). (1996). Concise Polymeric Materials Encyclopedia. CRC Press.
🎯 Final Thoughts: Commitment Starts at the Molecular Level
In an industry where “drop-in solutions” come and go, BDMPU stands out by doing something radical: it stays.
It doesn’t evaporate. It doesn’t bloom. It doesn’t wake up one day and decide to leach into your drinking water. It builds stronger networks, resists water’s advances, and keeps your product performing—year after year.
So next time you’re battling hydrolysis, chasing longer lifespan, or dodging VOC regulations, ask yourself:
“Am I using a catalyst… or am I using a partner?”
If the answer isn’t BDMPU, maybe it’s time for a relationship upgrade. 💍🧪
— Dr. Poly N. Mer, signing off with a full flask and a satisfied smile.
Sales Contact : sales@newtopchem.com
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