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4,4'-Cyclohexylidenebis(2-methylphenol)
[CAS# 2362-14-3]

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Complete supplier list of 4,4'-Cyclohexylidenebis(2-methylphenol)
Identification
Classification Organic raw materials >> Aryl compounds
Name 4,4'-Cyclohexylidenebis(2-methylphenol)
Synonyms 1,1'-Bis(4-hydroxy-3-methylphenyl)cyclohexane
Molecular Structure CAS # 2362-14-3, 4,4'-Cyclohexylidenebis(2-methylphenol), 1,1'-Bis(4-hydroxy-3-methylphenyl)cyclohexane
Molecular Formula C20H24O2
Molecular Weight 296.40
CAS Registry Number 2362-14-3
EC Number 219-110-7
SMILES CC1=C(C=CC(=C1)C2(CCCCC2)C3=CC(=C(C=C3)O)C)O
Properties
Solubility 0.3033 mg/L (25 ºC water)
Density 1.1±0.1 g/cm3, Calc.*
Index of Refraction 1.600, Calc.*
Melting point 180.92 ºC
Boiling Point 450.0±45.0 ºC (760 mmHg), Calc.*, 432.18 ºC
Flash Point 205.6±23.3 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
SDS Available
up Discovory and Applicatios
4,4'-Cyclohexylidenebis(2-methylphenol), commonly known as bis(2-methylphenol) cyclohexylidene or simply as bisphenol M, is an organic compound characterized by its unique molecular structure, which consists of two 2-methylphenol units linked by a cyclohexylidene bridge. This compound has garnered attention in various fields due to its remarkable chemical properties, particularly as a cross-linking agent and stabilizer in polymer chemistry.

The discovery of 4,4'-cyclohexylidenebis(2-methylphenol) dates back to the mid-20th century when researchers were exploring new phenolic compounds that could enhance the performance of resins and plastics. The interest in bisphenol derivatives stemmed from their ability to improve thermal stability, mechanical strength, and chemical resistance of materials. The synthesis of this compound involves the condensation reaction of 2-methylphenol with formaldehyde in the presence of an acid catalyst, followed by cyclization to form the cyclohexylidene linkage. This synthetic pathway enables the production of high-purity bisphenol M, which is crucial for its industrial applications.

One of the primary applications of 4,4'-cyclohexylidenebis(2-methylphenol) is in the formulation of thermosetting resins, particularly phenolic resins. These resins are widely used in the manufacturing of composite materials, adhesives, and coatings due to their excellent thermal and chemical resistance. The incorporation of bisphenol M into resin formulations significantly enhances their properties, leading to improved performance in high-temperature applications. This characteristic makes it particularly valuable in industries such as automotive, aerospace, and electronics, where materials must withstand harsh environments.

In addition to its role in resin production, bis(2-methylphenol) cyclohexylidene serves as a stabilizer in polymer systems. It helps prevent the degradation of polymers during processing and enhances their resistance to UV radiation and oxidative stress. This property is especially important in applications such as coatings, where prolonged exposure to sunlight and environmental conditions can lead to material deterioration. The use of bisphenol M as a stabilizer contributes to the longevity and durability of these products, making it an essential additive in various formulations.

Another area where 4,4'-cyclohexylidenebis(2-methylphenol) is gaining traction is in the development of biomaterials. Researchers are investigating its potential for use in biomedical applications, including drug delivery systems and tissue engineering. The compound’s biocompatibility and ability to form stable structures make it a promising candidate for creating scaffolds and matrices that support cell growth and tissue regeneration. Ongoing studies are focusing on optimizing its properties for these applications, highlighting the versatility of bisphenol M in the field of materials science.

Despite its numerous applications, the safety and environmental impact of 4,4'-cyclohexylidenebis(2-methylphenol) require careful consideration. Like many phenolic compounds, it may pose potential risks if not handled properly. Regulatory agencies are actively assessing its toxicity and environmental persistence to ensure safe usage in industrial and consumer products. This scrutiny emphasizes the importance of responsible chemical management and the need for alternatives that minimize environmental impact.

In summary, 4,4'-cyclohexylidenebis(2-methylphenol) is a valuable chemical substance with diverse applications in resin production, polymer stabilization, and potential biomedical uses. Its discovery has opened new avenues for the development of advanced materials that meet the demanding requirements of various industries. As research continues to uncover its potential, it is crucial to balance the benefits of bisphenol M with environmental and safety considerations.
Market Analysis Reports
List of Reports Available for 4,4'-Cyclohexylidenebis(2-methylphenol)
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