Reactive · PEGylated Stealth Copolymer

Poly(NHSMA-co-PEGMA)

Also written P(NHSMA-co-PEGMA), NHSMA-PEGMA copolymer  |  Custom composition — no single CAS

A random copolymer of N-hydroxysuccinimide methacrylate (NHSMA) and PEGMA (poly/oligo(ethylene glycol) methacrylate). PEGMA makes up the majority of the chain, grafting a dense, non-ionic PEG brush that sterically shields the backbone from protein and cell adhesion; NHSMA is included as a minor, sparsely distributed comonomer, each unit carrying a reactive NHS ester. The result is a stealth, PEGylated scaffold that stays “conjugation-ready” — couple the NHS sites to an amine-bearing ligand, antibody, dye, or drug without disturbing the PEG brush around it.

Custom composition

(C₈H₉NO₄)ₘ-co-[C₅H₈O₂-(C₂H₄O)ₓ-OCH₃]ₙ

Poly(NHSMA-co-PEGMA)

Poly(NHSMA-co-PEGMA) structure

Appearance: White to off-white powder
Character: PEG stealth + amine-reactive
Architecture: Random comb copolymer
Storage: -20 °C, dark, desiccated

ISO 9001:2015

Manufactured under certified quality management

Custom NHSMA:PEGMA Ratio

Reactive-site density tuned independently of PEG brush density

Batch-Level COA

Mn, Đ, composition, and NHS-ester activity per lot

Desiccated Cold-Chain Packaging

Preserves NHS-ester reactivity in transit and storage

CAS No.

Composition-dependent

Molecular Formula

(C₈H₉NO₄)ₘ-co-[C₅H₈O₂(C₂H₄O)ₓOCH₃]ₙ

Character

PEG stealth + amine-reactive

Mn Range

10K – 150K

Form

Powder

A stealth PEG brush with a few reactive handles

PEGMA and NHSMA aren't playing the same role here — one is the bulk material, the other is a sparse functional handle riding on top of it.

PEGMA: the stealth majority

Grafted PEG side chains hydrate and sterically shield the backbone from protein and cell approach — a non-ionic, charge-independent antifouling effect.

NHSMA: the sparse reactive minority

Each NHS ester reacts with a primary amine to install exactly one ligand, dye, or biomolecule per site — a small fraction of units is usually enough.

Ratio protects the PEG brush

Keeping NHSMA content low preserves a dense, contiguous PEG brush; too much reactive comonomer starts to thin out steric shielding.

Couple once, keep the brush intact

Reacting the NHS sites with your target amine doesn't touch the PEGMA units — the stealth behavior of the rest of the chain is unaffected.

≈2% NHSMA≈5%≈10%≈20%≈30%+ NHSMA
Maximum stealth, few sites Typical working range More sites, thinner PEG brush
Most reactive-PEGylated designs in the literature sit in the 2–15 mol% NHSMA range — enough reactive sites for practical conjugation density without materially thinning the PEG brush's steric shielding.

Choose the reactive-site density that fits your conjugate

NHSMA:PEGMA feed ratio sets how many reactive sites are available per chain, and how much that trades off against PEG brush density.

NHSMA : PEGMA ≈ 2:98

PEGMA-dominant

Maximum stealth coverage with just enough reactive sites for sparse, well-controlled single-ligand conjugation.

NHSMA : PEGMA ≈ 10:90

Balanced

A common working range — meaningful conjugation density (e.g. multiple dyes or ligands per chain) while retaining a strong PEG brush.

NHSMA : PEGMA ≈ 20:80

Reactive-rich

Higher reactive-site density for dense multivalent conjugation, with some reduction in steric shielding.

Applications

PEGylated drug conjugates

Amine-bearing drugs couple to the NHS sites while the PEG brush extends circulation and reduces immune recognition.

Antibody-PEG conjugates

Couples directly to antibody lysine amines, giving a PEGylated antibody with reduced immunogenicity and extended half-life.

Diagnostic microarrays

A low-background PEG surface with defined reactive spots for spotting amine-modified capture probes.

Reactive antifouling membranes

Membrane surface modification that resists biofouling while remaining chemically addressable for later functionalization.

Biosensor capture surfaces

Low-fouling PEG background minimizes nonspecific signal, while NHS sites give oriented, covalent capture-antibody immobilization.

Targeted stealth nanoparticles

A PEGylated, low-fouling corona with a small number of reactive sites for attaching a targeting ligand or antibody fragment.

Stealth polymersomes with ligands

PEG-shielded vesicles that carry a defined number of surface-conjugated targeting or imaging ligands.

PEGylated PPM libraries

One reactive-PEGylated precursor batch can be split and coupled to different amines to build a library of functionalized stealth materials.

Data & safety documents

Batch-specific COAs with GPC, composition (¹H-NMR), and NHS-ester activity data available for order confirmations. Contact us for a specific lot number.

Safety Data Sheet

GHS-format · EN / ZH

Certificate of Analysis

Ratio + Mw confirmation

Amine Coupling Protocol

Recommended buffers & conditions

FAQ

Most frequent questions and answers

It’s used wherever you need a low-fouling, PEGylated surface or particle that still needs to carry something specific — a targeting ligand, antibody, dye, or drug. The PEGMA brush keeps nonspecific protein and cell adsorption low, while the sparse NHS sites let you attach exactly what you need without giving up that stealth character.

PEGMA units are the stealth workhorse — a non-ionic, hydrated PEG side chain that sterically shields the backbone from nonspecific adsorption. NHSMA units are a minor, reactive comonomer — each carries an NHS ester that reacts with a primary amine. Combining them gives a low-fouling material that isn’t a dead end: it still has a defined way to attach something useful.

NHSMA is typically kept to a small minority — commonly 2–20 mol% — so the PEGMA brush still dominates the chain’s overall behavior. Higher NHSMA content gives more reactive sites per chain but starts to thin the PEG coverage, so the ratio is chosen based on how much conjugation density you actually need.

No — PEGMA units don’t carry primary amines or otherwise compete for the NHS ester, so they’re chemically inert to the coupling reaction itself. The main practical consideration is the same as for any NHS-ester chemistry: work in an amine-free buffer and avoid excess water exposure before coupling.

Dissolve the polymer fresh in a dry organic solvent (or briefly in a cold, amine-free aqueous buffer, pH 7.5–8.5) and add your amine-bearing target promptly — protein, peptide, dye, or small molecule. The amine displaces the NHS leaving group to form a stable amide bond at each reacted site.

No. Commercial mPEG-NHS reagents are typically small, discrete PEG molecules with a single NHS ester at one end, meant for one-to-one labeling. This copolymer is a polymer backbone carrying many PEGMA side chains for stealth plus a sparse number of NHS sites along the same chain — a multivalent scaffold rather than a single-conjugation reagent.

No — composition-specific random copolymers like this one are not assigned a single CAS Registry Number, since the NHSMA:PEGMA ratio, PEG chain length, Mn, and dispersity are set per synthesis batch. Each lot’s COA documents the actual composition and NHS-ester activity.

Store sealed, desiccated, at −20 °C, protected from light and moisture — the NHS ester is sensitive to both heat and humidity, and PEG side chains are themselves hygroscopic. Allow the container to reach room temperature before opening, dissolve fresh, and react promptly for best coupling efficiency.

Need a specific NHSMA:PEGMA ratio, or a pre-conjugated version?

Our technical sales team responds within one business day.