Zwitterionic Mucoadhesive Copolymer

Poly(MPC-co-AA)

Also listed as Poly(AA-co-MPC)  |  MPC monomer CAS 67881-98-5 · Acrylic acid monomer CAS 79-10-7

A random copolymer of MPC and acrylic acid (AA). Without MAA’s alpha-methyl group, the AA backbone is more flexible and gives a more uniform, tighter distribution of carboxyl groups along the chain — improving mucin binding and metal-ion chelation while keeping MPC’s antifouling hydration layer and a ready -COOH conjugation handle.

MPC CAS 67881-98-5

MPC — AA

Random copolymer, zwitterionic + anionic

Poly(AA-co-MPC)

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:AA Ratio

Charge density tunable to your spec

Batch-Level COA

Ratio and Mw confirmation per lot

Sample to Bulk

1 g R&D vials up to multi-gram supply

MPC Monomer CAS

67881-98-5

AA Monomer CAS

79-10-7

Character

Zwitterionic + anionic

Approx. pKa

~4.25

Package

1g / 10g / 100g

Why choose acrylic acid over methacrylic acid

These two are close cousins, so the choice usually comes down to one structural difference: the alpha-methyl group.
PropertyPoly(MPC-co-AA)Poly(MPC-co-MAA)
BackboneNo alpha-methyl — more flexibleAlpha-methyl — more sterically hindered
Carboxyl distributionMore uniform, tighter spacingSlightly more irregular
Approx. pKa~4.25~4.5 – 5.0
Best suited forMucoadhesion, ion chelationBioconjugation, general pH-triggered release
Precedented useOphthalmic/nasal/buccal mucoadhesive gels (Carbomer/PAA family)Broader pH-responsive drug-delivery research
Both carry a -COOH conjugation handle and MPC's antifouling background — the difference is in backbone flexibility and charge-group spacing, which is what drives the mucoadhesion and chelation advantage of AA.

Choose your ratio by function

More AA means stronger mucoadhesion and ion-binding capacity; more MPC means stronger baseline antifouling performance.

AA-light

Antifouling-dominant

Mostly MPC character — strong baseline protein resistance with a modest mucoadhesive/chelation handle.

Balanced

Dual-function grade

Standard grade for most mucoadhesive delivery and ion-chelation applications.

AA-rich

Mucoadhesion-dominant

Stronger mucin binding and ion chelation, with reduced antifouling background.

Applications

Ophthalmic mucoadhesive gels

Carboxyl groups hydrogen-bond with ocular mucin, extending residence time of eye-drop formulations.

Nasal & buccal drug delivery

Improves mucosal retention for intranasal or oral-mucosal formulations while resisting nonspecific protein fouling.

Metal-ion chelation

Uniform carboxyl spacing gives efficient binding of select metal ions for sensing or capture research.

pH-triggered drug delivery

Carboxyl ionization near physiological pH supports pH-responsive release designs.

Conjugation-ready nanoparticles

Antifouling MPC background plus a -COOH handle for attaching targeting ligands or fluorophores.

Layer-by-layer assembly

Anionic charge supports electrostatic layer-by-layer coating with cationic polymers.

Smart hydrogels

pH-triggered swelling behavior for stimuli-responsive matrices and sensors.

Antifouling biosensor surfaces

Low nonspecific background from MPC plus a covalent attachment site from AA for capture-molecule immobilization.

Data & safety documents

Batch-specific COAs confirm MPC:AA 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, AA 79-10-7) provided for reference.

AA lacks the alpha-methyl group that MAA has, so the backbone is more flexible and the carboxyl groups are spaced more uniformly along the chain. This tends to give AA-based copolymers an edge in mucoadhesion and metal-ion chelation, while MAA is more commonly used for general pH-triggered release and bioconjugation work. Both carry the same -COOH conjugation handle.

Ionized carboxyl groups form hydrogen bonds with mucin glycoproteins, and acrylic acid’s flexible, uniformly spaced carboxyls make this interaction especially effective — the same underlying chemistry behind Carbomer/polyacrylic acid gels already used in ophthalmic and mucosal formulations.

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. Pre-activated NHS-ester derivatives are available on request.

Both, in a sense — the MPC units are individually zwitterionic (net-neutral), while the AA units carry an ionizable carboxyl group. Above the carboxyl’s pKa (~4.25), the copolymer picks up net negative charge on top of its zwitterionic background.

Store at -20°C, sealed, and protected from moisture. In solution, buffer pH affects both mucoadhesive/chelation behavior and antifouling performance, so confirm your working pH range before formulation.

Need a custom MPC:AA ratio or an activated -COOH derivative?

Our technical sales team responds within one business day.