Molecular structure of 2,5-Dimethyl-2,5-hexanediol, CAS Number: 110-03-2
2,5-Dimethyl-2,5-hexanediol (CAS 110-03-2)
CAS Number:
110-03-2
Molecular Weight:
146.23
Molecular Formula:
(CH3)2C(OH)CH2CH2C(OH)(CH3)2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2,5-Dimethyl-2,5-hexanediol functions as a stabilizer and a solvent in various experiments. It acts by forming hydrogen bonds with water molecules, which helps to solubilize hydrophobic compounds and enhance their stability. 2,5-Dimethyl-2,5-hexanediol serves as a reducing agent, participating in redox reactions by donating electrons to other molecules. 2,5-Dimethyl-2,5-hexanediol can act as a chelating agent, binding to metal ions and preventing them from participating in unwanted chemical reactions. Its mode of action involves interacting with other molecules at the molecular level, altering their chemical properties and enhancing the stability of experimental systems.
2,5-Dimethyl-2,5-hexanediol (CAS 110-03-2) References
- Synthesis of a new fluorine-18-labeled bexarotene analogue for PET imaging of retinoid X receptor. | Wang, M., et al. 2014. Bioorg Med Chem Lett. 24: 1742-7. PMID: 24602901
- A green approach towards adoption of chemical reaction model on 2,5-dimethyl-2,5-di-(tert-butylperoxy)hexane decomposition by differential isoconversional kinetic analysis. | Das, M. and Shu, CM. 2016. J Hazard Mater. 301: 222-32. PMID: 26368796
- (Solid + liquid) phase equilibria and enthalpy changes in (water + 2,2-dimethyl-1,3-propanediol) | J. Bevan Ott, J. Rex Goates, Earl M. Woolley, Jeffrey G. Priest. 1982. The Journal of Chemical Thermodynamics. 14: 1077-1082.
- Thermally depolymerizable polycarbonates. 2. Synthesis of novel linear tertiary copolycarbonates by phase-transfer catalysis | F. M. Houlihan, F. Bouchard, J. M. J. Frechet, and C. G. Willson, et al. 1986. Macromolecules. 19: 13–19.
- Diols as effective oocatalysts in the phase transfer catalyzed preparation of 1-alkynes from 1,2-dihalides | Eckehard V. Dehmlow ∗, Rainer Thieser, Yoel Sasson, Ronny Neumann. 1986. Tetrahedron. 42: 3569-3574.
- The metabolism of 2, 5-dimethylhexane in male Fischer 344 rats | M.Paul Serve a, Daniel D. Bombick a, J. Roberts a, Gayle A. McDonald a, David R. Mattie b, Kyung O. Yu ∗ b. 1991. Chemosphere. 22: 77-84.
- Transformation of diols in the presence of heteropoly acids under homogeneous and heterogeneous conditions | Béla Török, Imre Bucsi, Tímea Beregszászi, Irén Kapocsi, Árpád Molnár. 1996. Journal of Molecular Catalysis A: Chemical. 107: 305-311.
- Selective synthesis of binuclear N-substituted tetrazoles and tetrazolium salts | P. N. Gaponik, S. V. Voitekhovich & A. S. Lyakhov. 2000. Chemistry of Heterocyclic Compounds. 36: 326–333.
- Crystal structure of first- and second-sphere complexes of uranyl nitrate with 1,2- and 1,4-diols | Claude Villiers, Pierre Thuéry, Michel Ephritikhine. 2004. Polyhedron. 23: 1613-1618.
- The Synthesis and Spectroscopic Characterization of Heterobimetallic Bu2Sn(IV) Complexes Derived from Some Chelating Ligands | Nandu Bala Sharma, Anirudh Singh & Ram C. Mehrotra†. 2006. Phosphorus, Sulfur, and Silicon and the Related Elements. 181: 1527-1539.
- Synthesis of 2,5-Dichloro-2,5-dimethylhexane by an SN1 Reaction | Carl E. Wagner* and Pamela A. Marshall. 2010. J. Chem. Educ. 87: 81–83.
- Cyclization of alkanediols in high-temperature liquid water with high-pressure carbon dioxide | Aritomo Yamaguchi, Norihito Hiyoshi, Osamu Sato, Masayuki Shirai. 2012. Catalysis Today. 185: 302-305.
- Photocatalytic carbon–carbon bond formation with concurrent hydrogen evolution on the Pt/TiO2 nanotube | Jian Wang a b c, Pengju Yang a, Baoyue Cao a, Jianghong Zhao a, Zhenping Zhu a. 2015. Applied Surface Science. 325: 86-90.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,5-Dimethyl-2,5-hexanediol, 100 g | sc-223474 | 100 g | $30.00 | |||
2,5-Dimethyl-2,5-hexanediol, 500 g | sc-223474A | 500 g | $90.00 |