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HS Code |
597326 |
| Cas Number | 591-68-4 |
| Molecular Formula | C9H10O |
| Molar Mass | 134.18 g/mol |
| Iupac Name | 3,5-Dimethylbenzaldehyde |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 228-229 °C |
| Melting Point | 29-32 °C |
| Density | 1.01 g/cm³ |
| Solubility In Water | Insoluble |
| Flash Point | 106 °C |
| Refractive Index | 1.543 |
| Pubchem Cid | 11922 |
As an accredited 3,5-Dimethylbenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a secure screw cap, clearly labeled "3,5-Dimethylbenzaldehyde," includes hazard warnings and CAS number. |
| Shipping | 3,5-Dimethylbenzaldehyde is shipped in tightly sealed containers, protected from light and moisture, and labeled according to hazardous material regulations. Packaging complies with international shipping standards for chemicals, ensuring safe transport. Handle with care, keeping away from incompatible substances, heat, and ignition sources. Appropriate documentation and hazard labeling are included. |
| Storage | 3,5-Dimethylbenzaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it away from strong oxidizing agents and acids. Ensure proper labeling and secondary containment to prevent leaks or spills. Use appropriate safety measures and store in accordance with local regulations and guidelines. |
Applications of 3,5-Dimethylbenzaldehyde in Industrial ManufacturingAs a direct manufacturer, we supply 3,5-Dimethylbenzaldehyde for select downstream industries that require consistent purity, reliable supply, and full regulatory traceability in their own processing lines. Below we detail key application scenarios where this material is in established use, including industry standards, integration steps, dosage guidance, and typical finished goods. 1. Fragrance Intermediate ProductionOur 3,5-Dimethylbenzaldehyde enables the synthesis of specialty aroma molecules as an intermediate in controlled perfumery and flavor manufacturing. Downstream processors value its stability under reaction conditions for constructing methylated aromatic profiles in high-grade fragrances, particularly those with woody or fruity tonalities. This aromatic aldehyde enters esterification, condensation, or cyclization reactions for creating proprietary ingredients, later compounded into fine fragrances and flavoring agents for the food and beverage sector. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ our 3,5-Dimethylbenzaldehyde in the synthesis of specific API precursors, including intermediates for antihypertensive and anti-inflammatory compounds. The aldehyde’s aldehydic reactivity and steric profile suit condensation, reduction, and heterocycle formation steps within multi-stage synthesis protocols. Our product guarantees analytical documentation and batch consistency to support validation processes in GMP-regulated facilities. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Building Block ManufacturingMajor crop protection producers utilize our 3,5-Dimethylbenzaldehyde as a core building block in the synthesis of select fungicide, herbicide, and pesticide actives. The methylated aromatic aldehyde structure is leveraged in multi-component reactions—often as a precursor for introducing electron-donating groups—thereby tuning downstream compound selectivity and functional group compatibility in agrochemical formulations subjected to rigorous regulatory evaluations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. High-Performance Polymer Modifier SynthesisEngineered plastics and specialty resin producers incorporate our material in the manufacture of polymer modifiers and cross-linking agents. The presence of dual methyl substituents facilitates controlled polymer side-chain modifications for improved flexibility, chemical resistance, and thermal stability. Downstream processes include polyester, epoxy, and polyurethane resin synthesis, where this aldehyde’s reactive carbonyl participates either in initial branching reactions or end-cap curing profiles targeting demanding automotive and electronics markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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