Zwitterionic pH-Responsive Copolymer
Poly(MPC-co-MAA)
Also listed as Poly(MAA-co-MPC) | MPC monomer CAS 67881-98-5 · MAA monomer CAS 79-41-4
A random copolymer combining MPC’s cell-membrane-mimetic antifouling surface with methacrylic acid’s ionizable carboxyl groups. The result is a protein-resistant backbone that also switches charge and swelling behavior with pH — and gives you a -COOH handle for further bioconjugation.
- Configurable MPC:HEMA ratio, custom Mw available
MPC CAS 67881-98-5
MPC — MAA
Random copolymer, zwitterionic + anionic
Appearance: White to off-white powder
Character:Zwitterionic + pH-anionic
Reactive Group: -COOH (conjugation-ready)
Storage: -20 °C, keep dry
ISO 9001:2015
Manufactured under certified quality management
Custom MPC:MAA Ratio
Charge density tunable to your spec
Batch-Level COA
Spectral data and free-dye content per lot
Sample to Bulk
1 g R&D vials up to multi-gram supply
MPC Monomer CAS
67881-98-5
MAA Monomer CAS
79-41-4
Approx. pKa
4.5 – 5.0
Character
Zwitterionic + anionic
Package
1g / 10g / 100g
Two functions in one backbone
MPC and MAA each contribute something different — together they give you an antifouling surface that also responds to its environment.
MAA: pH-responsive switch
The carboxyl group ionizes above its pKa (~4.5–5), so the chain shifts from compact/neutral at low pH to charged/extended near physiological pH.
MPC: antifouling background
The phosphorylcholine head group binds a hydration layer that resists nonspecific protein and cell adhesion, the same mechanism as our pMPC and MPC-HEMA grades.
Ready conjugation site
The same -COOH group used for pH-response also gives you a standard EDC/NHS handle to attach ligands, peptides, or drug payloads.
Electrostatic complexation
Ionized carboxyl groups can form polyelectrolyte complexes with cationic drugs, peptides, or polymers for co-assembly and delivery.
Exact pKa and swelling behavior shift with MPC:MAA ratio — reported on the batch technical data sheet.
Typical values for our standard grade. MPC:MAA ratio and molecular weight are configurable — request a batch-specific COA for your exact build.
Synonyms | Poly(MAA-co-MPC) · MPC-MAA copolymer · pH-responsive zwitterionic copolymer · Carboxyl-functionalized PC polymer |
|---|---|
| MPC Monomer CAS | 67881-98-5 |
| MAA Monomer CAS | 79-41-4 |
| MPC Monomer Formula | C₁₁H₂₂NO₆P, MW 295.27 g/mol |
| MAA Monomer Formula | C₄H₆O₂, MW 86.09 g/mol |
| Copolymer Type | Random (statistical) copolymer |
| Appearance | White to off-white powder |
| Character | Zwitterionic (MPC) + weak anionic, pH-responsive (MAA) |
| Approx. pKa (carboxyl) | 4.5 – 5.0 |
| MPC:MAA Ratio | Configurable — specify at order |
| Reactive Group | -COOH, available for EDC/NHS conjugation |
| Molecular Weight | Custom Mw available; specify at order |
| Solubility | Water-soluble, pH-dependent (more soluble above pKa) |
| Storage Conditions | -20 °C, sealed, protected from moisture |
| Package Sizes | 1 g, 10 g, 100 g per bottle |
Need a specific MPC:MAA ratio or an activated -COOH derivative (e.g. NHS ester)? Talk to technical sales →
Choose your ratio by function
More MAA means stronger pH-sensitivity and more conjugation sites; more MPC means stronger baseline antifouling performance.
MAA-light
Antifouling-dominant
Mostly MPC character — strong baseline protein resistance with a modest pH/conjugation handle.
Balanced
Dual-function grade
Standard grade for most pH-responsive, conjugation-ready delivery applications.
MAA-rich
pH-response-dominant
Stronger charge switching and more -COOH sites, with reduced antifouling background.
Applications
pH-triggered drug delivery
Carboxyl ionization at target pH (e.g. tumor, endosomal, or GI environments) drives payload release or particle destabilization.
Conjugation-ready nanoparticles
Antifouling MPC background plus a -COOH handle for attaching targeting ligands, peptides, or fluorophores.
Mucoadhesive formulations
Ionized carboxyl groups hydrogen-bond with mucin, aiding retention on mucosal surfaces for oral or nasal delivery.
Smart hydrogels
pH-triggered swelling/deswelling behavior for stimuli-responsive drug-release matrices and sensors.
Layer-by-layer assembly
Anionic charge supports electrostatic layer-by-layer coating with cationic polymers for multilayer surface engineering.
Antifouling biosensor surfaces
Low nonspecific background from MPC plus a covalent attachment site from MAA for capture-molecule immobilization.
Enteric-adjacent coatings
pH-dependent solubility profile supports GI-targeted coating designs alongside established enteric polymers.
Ion/metal complexation
Carboxyl groups chelate select metal ions, useful for metal-ion sensing or capture research.
Data & safety documents
Batch-specific COAs confirm MPC:MAA ratio and molecular weight. Contact us for a particular lot number.
Safety Data Sheet
GHS-format · EN / ZH
Certificate of Analysis
Ratio + Mw confirmation
¹H-NMR Spectrum
Structure confirmation
FAQ
Most frequent questions and answers
No — as a random copolymer with a configurable monomer ratio, it doesn’t have one universal CAS Registry Number. It’s identified by catalog number, with the monomer CAS numbers (MPC 67881-98-5, MAA 79-41-4) provided for reference.
Both, in a sense — the MPC units are individually zwitterionic (net-neutral), while the MAA units carry an ionizable carboxyl group. Above the carboxyl’s pKa, the copolymer picks up net negative charge on top of its zwitterionic background, so its overall charge is pH-dependent.
HEMA is a neutral, hydroxyl-bearing co-monomer that mainly adds hydrogel-forming structure. MAA is ionizable, so this phosphorylcholine-methacrylic acid copolymer adds pH-responsive charge switching and a reactive -COOH conjugation site that HEMA doesn’t provide. Choose HEMA for a neutral structural hydrogel, MAA for pH-triggered or conjugation-ready applications.
Standard EDC/NHS coupling chemistry works directly on the carboxyl groups — activate with EDC and NHS (or Sulfo-NHS), then react with a primary amine on your ligand, peptide, or drug. We can also supply pre-activated NHS-ester derivatives on request.
The carboxyl groups have an approximate pKa of 4.5–5.0. Below that pH they’re largely protonated and the chain is more compact; above it they ionize and the chain becomes more charged and extended. Exact transition pH shifts slightly with MPC:MAA ratio and ionic strength.
Store at -20°C, sealed, and protected from moisture. In solution, buffer pH affects both antifouling performance and charge state, so we recommend confirming your working pH range before formulation.