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Catalog Number:
39686
CAS Number:
1633-78-9
6-Mercapto-1-hexanol
Purity:
≥ 97% (CG)
Synonym(s):
6-hydroxy-1-hexanethiol, 6-Mercaptohexane-1-ol
Hazmat
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$45.00 /5G
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Informations sur le produit

6-Mercapto-1-hexanol is a versatile thiol compound known for its unique properties and applications in various industries. With a molecular structure that includes a sulfhydryl group, this compound is particularly valued in the fields of organic synthesis and materials science. Its ability to form stable thiol-ether linkages makes it an excellent candidate for use in the production of polymers, coatings, and adhesives, enhancing their durability and performance. Additionally, 6-Mercapto-1-hexanol is utilized in the formulation of specialty chemicals and as a reagent in biochemical research, where it serves as a reducing agent and a stabilizer for metal nanoparticles.

Researchers and industry professionals appreciate 6-Mercapto-1-hexanol for its functional versatility and effectiveness in modifying surfaces and enhancing chemical reactivity. Its applications extend to the development of biosensors and drug delivery systems, where its thiol functionality can facilitate conjugation with various biomolecules. The compound's unique properties not only improve product performance but also offer innovative solutions in the synthesis of advanced materials, making it a valuable addition to any chemical toolkit.

Numéro CAS 
1633-78-9
Formule moléculaire
C 6 H 14 OS
Poids moléculaire 
134.24
Informations générales
Numéro CAS 
1633-78-9
Formule moléculaire
C 6 H 14 OS
Poids moléculaire 
134.24
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

6-Mercapto-1-hexanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders, due to its ability to form stable thiol linkages.
  • Bioconjugation: Its thiol group allows for efficient conjugation with proteins and peptides, making it valuable in the development of targeted drug delivery systems and diagnostic agents.
  • Material Science: Used in the formulation of polymeric materials, it enhances the properties of coatings and adhesives, providing improved adhesion and durability.
  • Analytical Chemistry: As a reagent, it is employed in the detection of heavy metals and other contaminants in environmental samples, offering a reliable method for monitoring pollution levels.
  • Cosmetic Applications: Its antioxidant properties make it beneficial in cosmetic formulations, helping to protect skin from oxidative stress and improving product stability.

Citations