The melting point of dimethoxybenzene, also known as o-dimethoxybenzene or 1,2-dimethoxybenzene, is 92-93°C. This compound is a clear, colorless liquid with a sweet, floral aroma. It is soluble in most organic solvents, but insoluble in water.
Dimethoxybenzene is a member of the family of compounds known as aromatic hydrocarbons, which are characterized by the presence of a ring of carbon atoms bonded to each other in a particular arrangement. Aromatic hydrocarbons are known for their stability and low reactivity, which makes them useful as solvents and intermediates in chemical synthesis.
The melting point of a compound is the temperature at which it transitions from a solid to a liquid. It is determined by the strength of the intermolecular forces that hold the molecules of the compound together. In general, compounds with strong intermolecular forces have higher melting points than those with weaker forces.
In the case of dimethoxybenzene, the melting point is relatively low compared to other aromatic hydrocarbons. This is due in part to the presence of the two methoxy groups, which disrupt the aromatic ring and weaken the intermolecular forces. As a result, dimethoxybenzene has a lower melting point and is more readily converted to a liquid state than compounds with a more stable aromatic ring.
In addition to its low melting point, dimethoxybenzene is also known for its low boiling point. It vaporizes easily at room temperature, making it a useful solvent for a variety of chemical reactions. It is also used as a flavor and fragrance ingredient in the food and cosmetics industries.
In summary, dimethoxybenzene is a clear, colorless liquid with a sweet, floral aroma and a melting point of 92-93°C. It is a member of the aromatic hydrocarbon family and is known for its low melting and boiling points, as well as its use as a solvent and flavor/fragrance ingredient.
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Environmental fate and pathways This section provides environmental fate and pathways information compiled from all registered dossiers for the substance. The Agency thus cannot guarantee the correctness of the information displayed. A 114 1 , 209-17, 2010 Dichlorocarbene CCl 2 , generated by laser flash photolysis of dichlorodiazirine, formed pi- and O-ylidic complexes with aromatic ethers such as anisole, 1,3-dimethoxybenzene, 1,3,5-trimethoxybenzen. Ecotoxicological information This section summarises the Ecotoxicological information provided from all registered dossiers for the substance. Study results Displayed are the RANGES of min — max of values provided in %.
Brief Profile
Study results If more than one numerical result is available per endpoint, the range of results min-max and range of experimental conditions will be presented RANGE method. Data is generally standardised and displayed in milligram per litre or molar per litre. This section provides ecotoxicological information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. Study results If more than one value is available, results are displayed as concatenated distinct values, ordered from most to least commonly provided, with the percentage of provided values appended. If more than one picklist value is available per endpoint, results are displayed as concatenated distinct values, ordered by most to least commonly provided, with the % of provided values appended.
See the official CAS Chemical Abstract Service registry number The CAS number is the substance numerical identifier assigned by the Chemical Abstract Service, a division of the American Chemical Society, to substances registered in the CAS registry database. Type of study provided This section provides an overview of the type of study records behind the presented results and — if applicable - data waving justifications. Other identifiers gives any other non-name identifiers available for ths substance. The BPR addresses the placing on the market and use of biocidal products, which are used to protect humans, animals, materials or articles against harmful organisms, like pests or bacteria, by regulating the active substances contained in a biocidal product. Note: Results without a concentration value are not processed for the Brief Profile. NIST Mass Spectrometry Data Center. WARNING: The information provided on this web site was developed in compliance with European Union EU regulations and is correct to the best of our knowledge, information and belief at the date of its publication.
