Cas no 129475-75-8 (2-(2-methylbutyl)cyclohexan-1-ol)
2-(2-methylbutyl)cyclohexan-1-ol Chemical and Physical Properties
Names and Identifiers
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- Cyclohexanol, 2-(2-methylbutyl)-
- 2-(2-methylbutyl)cyclohexan-1-ol
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- Inchi: 1S/C11H22O/c1-3-9(2)8-10-6-4-5-7-11(10)12/h9-12H,3-8H2,1-2H3
- InChI Key: DZVUYRSRMDBYHG-UHFFFAOYSA-N
- SMILES: C1(O)CCCCC1CC(C)CC
Experimental Properties
- Density: 0.891±0.06 g/cm3(Predicted)
- Boiling Point: 226.3±8.0 °C(Predicted)
- pka: 15.32±0.40(Predicted)
2-(2-methylbutyl)cyclohexan-1-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1634268-0.05g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 0.05g |
$768.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-0.1g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 0.1g |
$804.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-0.25g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 0.25g |
$840.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-0.5g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 0.5g |
$877.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-1.0g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 1.0g |
$914.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-2.5g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 2.5g |
$1791.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-5.0g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 5.0g |
$2650.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-10.0g |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 10.0g |
$3929.0 | 2023-07-10 | ||
| Enamine | EN300-1634268-50mg |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 50mg |
$468.0 | 2023-09-22 | ||
| Enamine | EN300-1634268-100mg |
2-(2-methylbutyl)cyclohexan-1-ol |
129475-75-8 | 100mg |
$490.0 | 2023-09-22 |
2-(2-methylbutyl)cyclohexan-1-ol Related Literature
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
Additional information on 2-(2-methylbutyl)cyclohexan-1-ol
Comprehensive Overview of 2-(2-methylbutyl)cyclohexan-1-ol (CAS No. 129475-75-8): Properties, Applications, and Industry Trends
2-(2-methylbutyl)cyclohexan-1-ol (CAS No. 129475-75-8) is a versatile organic compound with a unique molecular structure that combines a cyclohexanol backbone with a branched alkyl substituent. This terpene-derived alcohol has garnered significant attention in recent years due to its potential applications in fragrances, flavorings, and specialty chemicals. The compound's stereochemistry and hydrophobic properties make it particularly interesting for researchers exploring novel bioactive molecules and green chemistry solutions.
The growing demand for sustainable aroma chemicals has positioned 2-(2-methylbutyl)cyclohexan-1-ol as a promising candidate in the fragrance industry. With consumers increasingly seeking natural-inspired scents and eco-friendly formulations, this compound's woody, earthy olfactory profile aligns perfectly with current market trends. Analytical studies using GC-MS techniques have demonstrated its stability in various formulations, while structure-activity relationship research continues to uncover new potential applications.
From a synthetic chemistry perspective, 129475-75-8 presents fascinating challenges and opportunities. Recent advancements in asymmetric synthesis have enabled more efficient production routes, addressing the compound's stereoisomer complexity. The pharmaceutical industry has shown interest in its derivatives as potential chiral building blocks for drug development, particularly in the creation of terpenoid-based therapeutics with improved bioavailability.
In material science applications, researchers are investigating 2-(2-methylbutyl)cyclohexan-1-ol as a precursor for biodegradable polymers and specialty coatings. Its molecular architecture offers unique possibilities for creating materials with tailored hydrophobic surfaces, relevant to marine coatings and water-repellent textiles. These developments align with global initiatives for sustainable material innovation and circular economy principles.
The compound's safety profile and environmental fate have been subjects of recent studies, particularly regarding its biodegradation pathways and ecotoxicological impact. Regulatory agencies are increasingly focusing on green chemistry metrics for such substances, making life cycle assessment data crucial for industrial adoption. Current research suggests favorable environmental persistence characteristics compared to traditional synthetic alternatives.
Analytical characterization of 129475-75-8 has benefited from modern spectroscopic techniques including advanced NMR methodologies and high-resolution mass spectrometry. These tools have enabled precise determination of its conformational dynamics and intermolecular interactions, providing valuable insights for formulation scientists. The compound's phase behavior in different solvent systems has become particularly relevant for extraction optimization processes.
Market analysts project steady growth for 2-(2-methylbutyl)cyclohexan-1-ol derivatives, driven by expanding applications in functional fragrances and advanced material science. The compound's compatibility with biobased solvents and renewable feedstocks positions it favorably in the shift toward sustainable chemical production. Industry stakeholders are particularly interested in its potential as a platform chemical for value-added products.
Future research directions for 129475-75-8 include exploring its role in catalysis applications and molecular recognition systems. The compound's structural features suggest possible utility in chiral separation media and asymmetric catalysis, areas of intense interest in pharmaceutical manufacturing. Additionally, its potential as a flavor modifier in food science applications warrants further investigation, particularly regarding structure-taste relationships.
Quality control protocols for 2-(2-methylbutyl)cyclohexan-1-ol production have evolved to include sophisticated chiral purity assessment methods and impurity profiling techniques. These advancements ensure consistent performance in end-use applications while meeting stringent industry standards for specialty chemicals. The development of robust analytical reference materials has been crucial for accurate quantification in complex matrices.
From a regulatory standpoint, 129475-75-8 benefits from favorable safety assessments in major markets, though regional differences in chemical registration requirements necessitate careful compliance strategies. The compound's inclusion in green chemistry databases and alternative assessment tools reflects its potential as a sustainable chemical option compared to conventional alternatives with greater environmental footprints.
In conclusion, 2-(2-methylbutyl)cyclohexan-1-ol represents an intriguing case study in the intersection of traditional chemistry and modern sustainability requirements. Its multifaceted applications across industries, combined with promising research developments, suggest a bright future for this versatile compound. As scientific understanding of its properties deepens and production methods become more efficient, we can anticipate expanded utilization of this molecule in innovative, environmentally conscious applications.
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