1,3-Dimethoxybenzene CAS 151-10-0
Name: 1,3-Dimethoxybenzene
CAS: 151-10-0
Purity: 99%min
MOQ: 1KG
Chemical Structure
Basic Info:
| CAS No: | 151-10-0 |
| Name: | 1,3-Dimethoxybenzene |
| EINECS: | 205-783-4 |
| Formula: | C8H10O2 |
| Weight: | 138.16 |
| Other Names: | Dimethyletherresorcinolu |
| Type: | Chemical reagents |
| Shelf Life: | 3 years |
| Brand Name: | Look Chem |
| Place of Origin: | Shandong, China |
Product Introduction:
Dimethyl ether, additionally referred to as 1,3-Dimethoxybenzene, is a fragrant natural substance. Its molecular framework is very instinctive: both hydrogen atoms in the meta setting (i.e. settings 1 and 3) on the benzene ring have actually been changed by a methoxy team (- OCH ∝), and the molecular formula is C8H10O2. 1,3-Dimethoxybenzene generally looks like an anemic to pale yellow clear liquid, with an unique scent comparable to fennel.
The chemical residential or commercial properties of this substance satisfy the regular features of aromatic ethers. The two methoxy teams on its body are particularly simple to give away electrons, and because they remain in the meta setting, they will considerably impact the electron circulation on the benzene ring, making it extra vulnerable to electrophilic substitution reactions, and the response setting is additionally very clear. When making it, resorcinol is normally used as the raw product and manufactured through methylation reaction, which is also a traditional technique in chemistry to convert phenolic hydroxyl groups into ether bonds.
Nature and Specifications:
Specification
Specification
| Item | Specification |
| Product Name | 1,3-Dimethoxybenzene |
| CAS No. | 151-10-0 |
| Appearance | Transparent Colorless Liquid |
| Shelf Life | 2 years |
| Packing | 1kg/bag,25kg/bag or as your requirements |
Product Packaging
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1,3-Dimethoxybenzene Uses:
1,3-Dimethoxybenzene is most definitely not a solitary use regular chemical. It gradually prolongs from the specific “response core” in standard organic synthesis to the “scent creator” in our sensory world, after that upgrades to the “architectural core” of cutting-edge materials, and ultimately integrates into the “energetic molecule design” connected to life and health. This collection of duty changes completely embodies the core concept of “structure establishes homes, buildings identify function” in chemistry. 1,3-Dimethoxybenzene is exactly as a result of its one-of-a-kind and steady aromatic ether structure that it plays numerous vital and irreplaceable duties in several areas of clinical research and market, becoming a traditional “bridge molecule” linking standard chemistry and numerous high-end application areas.
1,3-Dimethoxybenzene is not simply an average intermediate item, yet extra like a “molecular craftsman” proficient in precise positioning. Both methoxy groups on the benzene ring can provide electrons to the benzene ring, making it a highly electron rich aromatic system. This particular makes it highly reactive, conveniently responding with electrophilic reagents, and the responses are primarily concentrated at settings 4 and 6, with a particularly routine pattern. Chemists utilize this characteristic as a core design template to produce different complicated aromatic particles with distinctive frameworks and functional teams with timeless responses such as bromination, chloromethylation, and Claisen rearrangement. These molecules are essential web links in the synthesis of drugs, natural products, and advanced materials.
1,3-Dimethoxybenzene is a “little olfactory prize” with an one-of-a-kind scent. The scent it produces is moderate, sweet, and resilient, appearing like a mix of fennel and licorice, with a pure and passing through aroma. When preparing essence, it can play two roles: on the one hand, as the “major fragrance”, it can directly set or enhance the wonderful and organic sensation in essence; On the other hand, 1,3-Dimethoxybenzene can be used as a “taste fixative” due to its high boiling point and stable molecular framework, which can well mix other seasonings, reduce the exhaust rate of those conveniently volatilized flavors, and allow the taste of significance to stay longer. Whether it is perfume, cosmetics, soap or detergent, after adding it, the fragrance will be extra mellow and longer.
1,3-Dimethoxybenzene has developed from a little molecule to a crucial foundation for creating high-performance materials. Its molecular structure supplies an excellent bifunctional beginning factor for polymer developers. For instance, by oxidation response, 1,3-Dimethoxybenzene can be exchanged meta benzaldehyde, which can then undertake condensation response with bifunctional monomers such as diamines to produce polyimide or polyarylether materials including rigid benzene rings and ether bonds generally chain. This polymer is especially immune to heats, has high mechanical toughness, is dimensionally secure, and can also offer insulation. So when making substrates for versatile circuit boards, light-weight composite components for aerospace lorries, special insulation movies, and chemical immune finishings, it is a necessary premium core product.
1,3-Dimethoxybenzene its derivatives are several “aromatic skeletons” or “drug carriers” with naturally active molecules. Its benzene ring itself is a secure hydrophobic core, and the two methoxy teams are not quickly ruined by body metabolic rate, however can likewise create hydrogen bonds. Moreover, they can conveniently be chemically changed into crucial functional groups such as hydroxyl, aldehyde, and halogen. In drug growth, this structure is frequently made use of in the layout of central nerves medications, anti-biotics, and cardio medications. In the field of pesticides, compounds based upon it are often become reliable herbicide or fungicide prospects due to their one-of-a-kind structure and electronic residential or commercial properties, providing an important chemical basis for the advancement of new, low deposit green chemicals.
Related Industry Q&A
Q: What are the primary resources made use of for the manufacturing of 1,3-Dimethoxybenzene?
A: Primarily utilizing resorcinol as raw material, it can be created through methylation reaction (such as responding with dimethyl sulfate, iodomethane and various other compounds), which is also one of the most generally used and traditional approach in industry.
Q: What should be noted when keeping and delivering this product?
A: It needs to be kept in an awesome and aerated storehouse, away from resources of fire and warmth. It is a flammable fluid and a little bit bothersome. When running, put on protective devices, seal it well, and do not put it along with oxidants.
Q: What are its essential high quality standards?
A: The essential quality signs mainly consist of pureness (normally needed to be ≥ 99%), wetness material, color, as well as the content of contaminations such as residual resorcinol and methylation reagents. Gas chromatography (GC) is typically made use of for detection.
Q: What are the advantages of using it in spices?
A: The benefits are obvious. The aroma is stable and long-term, with pleasant fennel licorice taste and stable chemical buildings. It is challenging to weaken in the significance formula, and it can additionally well mix various other tastes, to ensure that the general scent lasts much longer.
Q: What is the most critical derivative downstream of it?
A: Among the most vital derivatives is meta benzaldehyde. This substance is an essential beginning material for manufacturing high-performance polymers (such as polyimides, specialty resins) and numerous pharmaceutical intermediates, with high value.
Related References:
1,3-Dimethoxybenzene Manufacturer & Supplier
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