Home » Products » Fine Chemicals » 2,6,7-Trioxa-1-phosphabicyclo2.2.2octane-4-methanol, 1-oxide
Appearance:White powder
Content:≥99.0%
| Product name | 2,6,7-Trioxa-1-phosphabicyclo2.2.2octane-4-methanol, 1-oxide |
| Synonym | 2,6,7-Trioxa-1-phosphabicyclo2.2.2octane-4-methanol, 1-oxide;(1-oxo-2,6,7-trioxa-1$l^{5}-phosphabicyclo[2.2.2]oct-4-yl)methanol |
| CAS NO. | 5301-78-0 |
| Appearance | White powder |
| Content | ≥99.0% |
| MF | C5H9O5P |
| MW | 180.1 |
| Related categories | Organic intermediates; Flame retardants; Heterocyclic compounds; Organic chemical raw materials; Chemical connection; Pharmaceutical intermediates; Fire retardants |
| Transport Information | no dangerous goods |
| HS Code | 2916140090 |
| Application | Polymer material reactive flame retardant modification Synthetic monomers of intrinsic flame-retardant polymers |
| Packaging | 100g/bottle;25.0kg/drum;100.0kg/drum |
| Contact Info | lucy@coreychem.com |
Appearance: Typically white or off-white crystalline powder.
Solubility: Soluble in polar solvents such as water, methanol, ethanol, dimethylformamide (DMF), and dimethyl sulfoxide (DMSO). Insoluble or poorly soluble in non-polar solvents (e.g., toluene, n-hexane). Its water solubility is a major advantage as a reactive flame retardant.
Characteristics:
High Phosphorus Content: Phosphorus content reaches ~15.8%, meaning effective flame retardancy can be achieved with lower addition levels.
Rigid Cage Structure: The bicyclic cage structure confers high thermal stability and rigidity, contributing to increased polymer glass transition temperature and dimensional stability.
Active functional groups: Terminal -CH₂OH (hydroxymethyl) groups enable covalent bonding to polymer chains through chemical reactions (e.g., esterification, etherification, condensation), integrating it as a polymer component.
The core value of PEPA-OH lies in its role as a “reactive” flame retardant monomer. It does not function as a simple additive but is permanently incorporated into the polymer matrix through chemical reactions.
Reactive Flame Retardant Modification of Polymeric Materials
Polyester (PET, PBT): PEPA-OH structures are incorporated into polyester molecular chains through copolymerization with dicarboxylic acids (or esters), producing inherently flame-retardant polyesters. Widely used in flame-retardant fibers, engineering plastics, and films.
Polyurethane (PU): As a polyol component, it reacts with isocyanates to produce inherently flame-retardant polyurethane foams, elastomers, coatings, and adhesives.
Epoxy Resins: It can function as a curing agent or modifier, participating in the curing network of epoxy resins to impart excellent flame retardancy, high Tg, and good mechanical properties to the cured material. Used in high-end electronic packaging materials and composites.
Acrylic Resin: Its hydroxymethyl groups react with acrylic (ester) to form phosphorus-containing acrylic monomers, which polymerize into flame-retardant coatings, adhesives, etc.
Essential synthetic monomers for intrinsically flame-retardant polymers
Serves as a key intermediate for synthesizing a series of novel phosphorus (phosphine)-containing ester polymers, used to prepare specialty engineering plastics with high thermal stability, low smoke emission, and low toxicity.
The flame retardant effect of PEPA-OH is primarily achieved through the following synergistic mechanisms:
Condensation-phase flame retardancy: During combustion, polymers containing PEPA structures decompose to form phosphoric acid or polyphosphoric acid compounds. These promote carbonization on the polymer surface, forming a dense, heat-insulating char layer that isolates oxygen and heat.
Gas-Phase Flame Retardation: Decomposition generates phosphorus-containing radicals (e.g., PO·), which capture high-energy H· and OH· radicals in the combustion chain reaction, interrupting flame propagation.
Thermal Stability: Its rigid structure elevates the material’s thermal decomposition temperature, delaying the thermal decomposition process.
5. Advantages over Additive-Type Flame Retardants
Durability: Chemically bonded, it does not migrate, volatilize, or leach out, ensuring long-lasting flame retardancy.
Excellent Compatibility: As an integral part of the polymer chain, it is fully compatible with the matrix, preserving material transparency, mechanical properties, and processability.
Environmental Friendliness: Eliminates potential environmental and health risks associated with small-molecule additive flame retardants.
Storage: Keep sealed in a cool, dry, well-ventilated area to prevent moisture absorption.
Stability: Structurally stable, but due to its hydroxyl group content, avoid contact with strong oxidizing agents, strong acids, and strong bases.
Safety: As a chemical, it may cause irritation to eyes, skin, and respiratory tract. Wear protective equipment during handling and operate within a fume hood.
For pricing, samples, technical data, or customized specifications, please contact:
●Product Manager:Lucy Yao
Email: lucy@coreychem.com
Packaging:500g/bottle;25.0kg/drum;100.0kg/drum
Customized packaging available upon request.