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  • 6920-22-5 , 1,2-己二醇, DL-1,2-Hexanediol, CAS:6920-22-5
6920-22-5 , 1,2-己二醇, DL-1,2-Hexanediol, CAS:6920-22-5

6920-22-5 , 1,2-己二醇, DL-1,2-Hexanediol, CAS:6920-22-5

6920-22-5 , 1,2-己二醇,
DL-1,2-Hexanediol,
CAS:6920-22-5
MFCD00010737
C6H14O2 / 118.17

1,2-己二醇

DL-1,2-Hexanediol

DL-1,2-Hexanediol is a skin-conditioning agent that has synergistic effects with cationic surfactants. It increases the hydrophobicity of the skin and enhances the binding of antimicrobial agents to skin cells. DL-1,2-Hexanediol also stimulates epidermal growth factor (EGF) production in human keratinocytes (HK-2) and may be useful for treating wounds or burns. The hydroxyl group on hexanediol provides a hydrophobic effect that is beneficial for skin care.

1,2-Hexanediol is a colorless, water-soluble, and viscous liquid organic compound with a molecular formula of C6H14O2. It is classified as an alcohol and commonly used as a solvent for various organic and inorganic compounds. The compound is also used as an intermediate in the production of other chemicals, including plasticizers, coatings, and adhesives. 1,2-Hexanediol was first synthesized in the early 1940s and has since become an essential compound in many chemical industries.

Physical and Chemical Properties:

1,2-Hexanediol has a melting point of -6°C and a boiling point of 250°C. It has a density of 0.94 g/cm3 and a vapor pressure of 0.0011 mmHg at 25°C. The molecular weight of 1,2-Hexanediol is 118.17 g/mol. This compound is soluble in water and other polar solvents and has a mild odor.

Synthesis and Characterization:

There are several methods for synthesizing 1,2-Hexanediol. One of the most common methods is the hydrogenation of adipic acid in the presence of a catalyst. Other methods include the reduction of ketones and aldehydes and the hydroformylation of olefins. The synthesis of 1,2-Hexanediol can be characterized by various analytical techniques, including gas chromatography (GC), liquid chromatography (LC), nuclear magnetic resonance (NMR) spectroscopy, and infrared spectroscopy (IR).

Analytical Methods:

Analytical methods are essential in determining the purity and concentration of 1,2-Hexanediol. Some of the commonly used techniques for this include GC, LC, NMR, and IR. GC and LC are used to identify and separate different components of the compound. On the other hand, NMR and IR spectroscopy are used to analyze the molecular structure of 1,2-Hexanediol.

Biological Properties:

1,2-Hexanediol has low toxicity to humans and animals. Studies have shown that the compound is not irritating to the skin and eyes. However, prolonged exposure can cause irritation and skin sensitization. There is also no evidence of carcinogenic, mutagenic, or reproductive toxic effects of 1,2-Hexanediol.

Toxicity and Safety in Scientific Experiments:

The use of 1,2-Hexanediol in scientific experiments should be done with care. The compound can be harmful if ingested, inhaled, or comes into contact with the skin. Proper protective equipment should be used when handling the compound. Further studies are necessary to investigate the long-term toxicity of 1,2-Hexanediol.

Applications in Scientific Experiments:

1,2-Hexanediol has various applications in scientific experiments. It is commonly used as a solvent for chromatography and electrophoresis techniques, including capillary electrophoresis and gel electrophoresis. The compound is also used in the synthesis of polymers, resins, and adhesives.

Current State of Research:

The current state of research on 1,2-Hexanediol focuses on its applications in various fields and the potential health and environmental impacts of the compound. Studies have shown its use in the synthesis of multi-functional materials that can be used for drug delivery, catalysis, and other applications.

Potential Implications in Various Fields of Research and Industry:

1,2-Hexanediol has potential implications in various fields of research and industry. For example, it can be used as a cosolvent in pharmaceutical formulations, and as a polymer additive for performance improvement. The compound can also be used as a moisturizer and emollient in the personal care industry, and as a lubricant and plasticizer in the commercial industry.

Limitations and Future Directions:

Although 1,2-Hexanediol has many potential applications, there are limitations to its use. For instance, it has a low boiling point, which limits its use in high-temperature applications. Furthermore, it is expensive compared to other solvents. However, there are still opportunities to improve its synthesis and optimize its applications. Future directions include exploring the use of 1,2-Hexanediol in the synthesis of novel materials with specialized properties, investigating its use in energy storage and conversion systems, and exploring its use in the agricultural industry, such as crop protection.

In conclusion, 1,2-Hexanediol is an essential compound with various potential applications in research and industry. The compound possesses unique physical and chemical properties, making it a valuable solvent and intermediate in the production of other chemicals. Further research is needed to optimize its use and improve its synthesis while ensuring the safety of its use.

CAS Number6920-22-5
Product Name1,2-Hexanediol
IUPAC Namehexane-1,2-diol
Molecular FormulaC6H14O2
Molecular Weight118.17 g/mol
InChIInChI=1S/C6H14O2/c1-2-3-4-6(8)5-7/h6-8H,2-5H2,1H3
InChI KeyFHKSXSQHXQEMOK-UHFFFAOYSA-N
SMILESCCCCC(CO)O
Synonyms(±)-Hexane-1,2-diol; 1,2-Dihydroxyhexane; 1,2-Hexyleneglycol; 5,6-Dihydroxyhexane; DL-1,2-Hexanediol; KMO 6
Canonical SMILESCCCCC(CO)O


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