CAS 1633-78-9
:6-Mercapto-1-hexanol
Description:
6-Mercapto-1-hexanol, with the CAS number 1633-78-9, is an organic compound characterized by the presence of a thiol (-SH) functional group and a hydroxyl (-OH) group, making it a member of the class of mercapto alcohols. This compound features a six-carbon straight-chain structure, which contributes to its hydrophilic properties due to the hydroxyl group, while the thiol group imparts distinct reactivity, particularly in forming disulfide bonds and participating in nucleophilic reactions. 6-Mercapto-1-hexanol is typically a colorless to pale yellow liquid with a characteristic odor, and it is soluble in water and organic solvents. Its applications span various fields, including organic synthesis, where it serves as a building block for more complex molecules, and in the development of materials, such as adhesives and coatings, due to its ability to form strong bonds with metals and other surfaces. Additionally, it may exhibit antioxidant properties, making it of interest in biochemical research.
Formula:C6H14OS
InChI:InChI=1S/C6H14OS/c7-5-3-1-2-4-6-8/h7-8H,1-6H2
InChI key:InChIKey=UGZAJZLUKVKCBM-UHFFFAOYSA-N
SMILES:C(CCCS)CCO
Synonyms:- 1-Hexanol, 6-mercapto-
- 1-Mercapto-6-hexanol
- 6-Hydroxy-1-Hexanethiol
- 6-Hydroxyhexyl mercaptan
- 6-Mercaptohexan-1-Ol
- 6-Mercaptohexanol
- 6-Sulfanylhexan-1-Ol
- Mercaptohexanol
- 6-Mercapto-1-hexanol
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Found 6 products.
6-Mercapto-1-hexanol
CAS:Formula:C6H14OSPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:134.246-Mercapto-1-hexanol
CAS:Formula:C6H14OSPurity:≥ 98.0%Color and Shape:Clear, colourless liquidMolecular weight:134.246-Mercapto-1-hexanol
CAS:Controlled Product<p>Applications 6-Mercapto-1-hexanolcan be used as a chemical linker for anchoring biological molecules to gold surfaces.<br>References McKinlay, C. J. et al.: J. Am. Chem. Soc 138, 3510 (2016)<br></p>Formula:C6H14OSColor and Shape:NeatMolecular weight:134.246-Mercapto-1-hexanol
CAS:<p>6-Mercapto-1-hexanol is a redox active molecule that has been shown to be a potent inhibitor of human immunodeficiency virus type 1 reverse transcriptase. It has also been shown to inhibit the polymerase chain reaction and transfer reactions, including those mediated by DNA-dependent RNA polymerase. 6-Mercapto-1-hexanol can be detected with high sensitivity in human serum, which is its main application for the diagnosis of HIV infection. This compound reacts with molecular oxygen to form superoxide radicals, which are responsible for its redox potential. The rate constant for this reaction has been shown to be dependent on pH and temperature. 6-Mercapto-1-hexanol can also form stable complexes with proteins such as albumin or human immunoglobulin G (IgG). These complexes have been shown to exhibit electrochemical impedance spectroscopy activity at low concentrations and chemical stability in biological media.</p>Formula:C6H14OSPurity:Min. 96%Color and Shape:Clear LiquidMolecular weight:134.24 g/mol





