Sodium Methallyl Sulfonate (SMAS)

Sodium Methallyl Sulfonate (SMAS)

Sodium Methallyl Sulfonate (SMAS)

Chemical Formula: C₄H₇NaO₃S
IUPAC Name: Sodium 2-methyl-2-propene-1-sulfonate
Structure: CH₂=C(CH₃)CH₂SO₃Na


1. Key Properties

  • Physical Appearance: White crystalline powder, highly hygroscopic.
  • Solubility: Freely soluble in water; forms a weakly alkaline solution.
  • Reactivity: Contains a reactive vinyl group (polymerizable) and a sulfonate group (ionic/hydrophilic).
  • Stability: Resistant to high temperatures, hydrolysis, and harsh chemical conditions.

2. Synthesis

SMAS is typically synthesized via the sulfonation of methallyl chloride:
Methallyl Chloride (CH₂=C(CH₃)CH₂Cl) + Sodium Sulfite (Na₂SO₃) → SMAS
The reaction requires controlled temperature and pH to maximize yield.


3. Applications

  • Polymer Industry:
    • Copolymerization monomer for acrylic fibers, styrene, and acrylate resins to enhance dyeability, antistatic properties, and thermal resistance.
    • Used in high-performance fibers (e.g., modified polyacrylonitrile).
  • Water Treatment:
    • Scale inhibitor and dispersant for Ca²⁺/Mg²⁺ in cooling/boiler systems.
  • Oilfield Chemicals:
    • Additive in drilling fluids and EOR (Enhanced Oil Recovery) for salt/heat resistance.
  • Other Uses:
    • Electroplating additives, paper strengthening agents, and coatings modification.

4. Advantages

  • High hydrophilicity: Sulfonate group improves water solubility and ionic conductivity.
  • Polymer versatility: Easily copolymerizes with acrylamide, acrylic acid, etc.
  • Robust performance: Stable under extreme pH/temperature conditions.

5. Safety & Handling

  • Toxicity: Low toxicity but may irritate eyes/skin (use PPE).
  • Storage: Keep sealed in dry, cool conditions to prevent moisture absorption.

6. Related Compounds

  • Analogues: Sodium Allyl Sulfonate (SAS), 2-Acrylamido-2-methylpropanesulfonic acid (AMPS).
  • Differentiator: SMAS’s methyl group lowers steric hindrance, enhancing reactivity.

SMAS is a critical monomer in functional polymers and industrial chemistry due to its dual functionality (vinyl + sulfonate). For technical specifications (e.g., polymerization kinetics), refer to supplier MSDS or chemical databases like PubChem.