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HS Code |
715983 |
| Chemical Name | 3-Methoxy-4-Methylbenzaldehyde |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.18 g/mol |
| Cas Number | 6736-85-2 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 257-259 °C |
| Density | 1.077 g/cm3 |
| Refractive Index | 1.545-1.547 |
| Smiles | COC1=CC(=C(C=C1)C)C=O |
As an accredited 3-Methoxy-4-Methylbenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package of 3-Methoxy-4-Methylbenzaldehyde comes in a sealed amber glass bottle with a hazard-labelled screw cap. |
| Shipping | 3-Methoxy-4-Methylbenzaldehyde is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. Packaging complies with international transport regulations for hazardous chemicals. The product is clearly labeled with hazard information and handled by trained personnel. Shipment includes safety data sheets, and temperature control may be applied if required. |
| Storage | 3-Methoxy-4-Methylbenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as oxidizing agents. Protect it from direct sunlight and moisture. Store at room temperature, and ensure proper labeling to prevent accidental misuse. Follow all local regulations and safety guidelines during handling and storage. |
Applications of 3-Methoxy-4-Methylbenzaldehyde in Industrial Manufacturing3-Methoxy-4-Methylbenzaldehyde serves as a specialized aromatic aldehyde intermediate in several high-value chemical sectors. Our manufacturing process ensures high purity and supply consistency, supporting industrial formulations under demanding regulatory and quality environments. The following are key downstream applications in which this material is essential. 1. Pharmaceutical Intermediate for Antihypertensive AgentsThe compound functions as a crucial intermediate in the synthesis of active pharmaceutical ingredients, notably for calcium channel blockers in antihypertensive drug manufacturing. Pharmaceutical companies incorporate it during multi-step organic synthesis routes, where stringent impurity limits apply. Our production supports compliance with validated synthetic pathways and repeatable batch-to-batch quality for regulated final dosage forms. Industry compliance standards
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2. Fragrance and Aroma Chemical ManufacturingDownstream specialty fragrance manufacturers apply this benzaldehyde derivative as a key note in floral, spicy, and sweet aromatic blends. It modulates and builds core aldehydic character in high-volume perfumery oils and also appears in compounded fragrance bases for personal care formulations. Processing conditions demand precise weighing and temperature control to ensure olfactory integrity through blending and storage cycles. Industry compliance standards
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3. Agrochemical Active Ingredient SynthesisThe chemical plays a role in the organic synthesis routes for crop protection actives, particularly in the preparation of selective herbicide or fungicide scaffolds. Downstream agrochemical plants incorporate it as a starting material for constructing benzene ring-substituted intermediates, which subsequently undergo further functionalization. Scalability and impurity profile directly impact yield and regulatory registration in key jurisdictions. Industry compliance standards
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4. Specialty Dye & Pigment IntermediateColorants and pigment manufacturers use the aldehyde group in this compound as a reactive functionality for producing complex organic dyes, especially in the synthesis of proprietary azo and anthraquinone dyes. The compound serves as a building block where controlled reactivity determines color stability and solubility. The presence and purity directly influence final pigment shade, application fastness, and dispersibility in downstream industrial applications. Industry compliance standards
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5. Fine Chemical Synthesis for Analytical ReagentsProducers of laboratory analytical reagents employ this molecule as an aldehydic substrate in the design of derivatization agents and chromogenic reagents. The controlled reactivity of the methoxy and methyl substituents allows for selective labeling or detection chemistry. Application requires high-purity supply and traceability, as analytical performance depends on strict residual impurity control and consistent physical characteristics across production lots. Industry compliance standards
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Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
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