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Burnt Type 1,6-Hexanedithiol CAS 1194-43-1 Flavor Intermediate as As a flavoring for chicken, beef, and dish seasonings
| Minimum Order Quantity | 10KG |
|---|---|
| Price | negociate |
| Packaging Details | plastic drums or IBC totes |
| Delivery Time | ONE WEEK |
| Payment Terms | T/T,L/C,D/A |
| Supply Ability | 300 TONS |
Product Details
| Boiling Point | 118-119 °C/15 MmHg (lit.) | Density | 0.983 G/mL At 25 °C (lit.) |
|---|---|---|---|
| FEMA | 3495 | Refractive Index | N20/D 1.511(lit.) |
| Flash Point | 195 °F | Odor | At 0.10 % In Propylene Glycol. Burnt Fatty Meaty Fungal Sulfurous |
| Fragrance Type | Burnt | Biological Source | Synthetic |
| LogP | 2.80 | Appearance | Clear Colorless To Slightly Yellow Liquid |
| Storage | RT, Stored Under Nitrogen | ||
| Highlight | CAS 1194-43-1 Flavor Intermediate,1 6-Hexanedithiol CAS 1194-43-1,burnt type 1 6-Hexanedithiol |
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Product Description
1,6-Hexanedithiol CAS 1194-43-1 - Flavor Intermediate
Product Overview
High quality flavor intermediate 1,6-Hexanedithiol CAS 1191-43-1, a specialized chemical compound used in flavor manufacturing applications.
Technical Specifications
| Product Name | 1,6-Hexanedithiol |
|---|---|
| Synonyms | 1,6-Dimercaptohexane; 1,6-Hexandithiol; 1,6-Hexanedithiol; Hexane-1,6-dithiol; Hexamethylendimercaptan; Hexamethylene Dimercaptan; FEMA 3495; 1,6-Hexanedimercaptan |
| CAS Number | 1191-43-1 |
| Molecular Formula | C6H14S2 |
| Molecular Weight | 150.31 |
| EINECS | 214-735-1 |
| Product Categories | Sulfides flavors; Industrial/Fine Chemicals; Phenoles and thiophenoles; API intermediates; thiol Flavor; Halogenated Heterocycles |
| Mol File | 1191-43-1.mol |
Key Characteristics
Odor Profile: Strong, unpleasant, and skunky. Like all low-molecular-weight thiols, it has a powerful, offensive odor due to the sulfur atoms. However, its odor is generally considered less intensely putrid than that of 2-Phenylethyl Mercaptan.
Applications
1 Self-Assembled Monolayers (SAMs)
1,6-Hexanedithiol is widely used to form SAMs on gold, silver, and other metal surfaces. The molecule binds via one thiol group to the metal surface, leaving the distal thiol free for subsequent functionalization, enabling:
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Fabrication of molecular junctions
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Immobilization of biomolecules or nanoparticles
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Formation of mixed monolayers with alkanethiols
2 Crosslinking Agent in Polymer Chemistry
As a bifunctional thiol, it serves as a crosslinker for:
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Epoxy resins (via thiol-epoxy click chemistry)
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Polyurethanes (chain extension)
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Vinyl polymers (thiol-ene photoclick reactions)
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Hydrogels for biomedical applications
3 Surface Functionalization
Used to introduce reactive thiol groups onto oxide surfaces (e.g., silica, ITO) after silanization with thiol-terminated silanes, or directly on metals.
4 Nanoparticle Stabilization and Assembly
Employed in the synthesis and assembly of gold nanoparticles (AuNPs), quantum dots, and other nanocrystals, either as a capping ligand or as a molecular linker for nanoparticle networks.
5 Organic Synthesis
Utilized as a protecting group for carbonyls (via cyclic thioketal formation) and as a building block for sulfur-containing heterocycles or macrocycles.
Packaging Options
Available in plastic drums, IBC totes, or customized packaging to meet specific requirements.
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