High-purity aliphatic thiol with consistent batch-to-batch reproducibility.
Excellent reactivity in thiol–ene click chemistry for controlled polymer functionalization.
Low odor profile relative to shorter-chain thiols, supporting safer handling in industrial settings.
Stable molecular structure enabling reliable performance in radical-mediated reactions.
Soluble in common organic solvents including THF, chloroform, and toluene.
Surface modification of nanoparticles and quantum dots for enhanced colloidal stability.
Chain-end capping agent in controlled/living radical polymerization (e.g., RAFT, ATRP).
Building block for synthesizing thiol-functionalized monomers and crosslinkers.
Intermediate in pharmaceutical and agrochemical synthesis requiring selective C–S bond formation.
Additive for specialty coatings and adhesives to improve substrate adhesion and cure kinetics.
| Chemical Type | Aliphatic thiol |
| Product Form | Liquid |
| Appearance | Pale yellow clear liquid |
| Molecular Formula | C8H18S |
| Molecular Weight | 146.29 g/mol |
| Boiling Point (at 760 mmHg) | 205–207 °C |
| Density (at 20 °C) | 0.829–0.833 g/cm³ |
| Refractive Index (n20D) | 1.452–1.456 |
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