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Available Variants1 g
CHA.58355-1g
Price
€218.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.58355-1g | €218.40 |
95%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | (CH3)3SiCH2CH2SH |
|---|---|
| CAS Number | 18143-30-1 |
| Molecular Weight | 134.32 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 24862451 |
| MDL number | MFCD00077888 |
| Beilstein/REAXYS Number | 1732126 |
| Assay | 95% |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS02
GHS07
  GHS02,GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H226,H315,H319,H335 |
| pcodes | P210 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 3 - Flammable liquids |
| wgk | WGK 3 |
| flash_point_f | 120.2 °F - closed cup |
| flash_point_c | 49 °C - closed cup |
| ppe | Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
2-(Trimethylsilyl)ethanethiol, with the CAS number 18143-30-1, is a chemical compound that has been utilized in various applications due to its unique properties. This organosilicon compound is characterized by the presence of a trimethylsilyl group attached to an ethanethiol moiety, which imparts distinct reactivity and stability. The compound has been employed as a precursor or intermediate in the synthesis of other organosilicon compounds, taking advantage of the facile cleavage of the silicon-sulfur bond under certain conditions. Additionally, 2-(trimethylsilyl)ethanethiol has been used in the modification of surfaces and materials, where its thiol functionality can participate in self-assembly or binding processes, while the trimethylsilyl group can influence the compounds solubility and volatility. Its chemical properties make it a valuable reagent in various fields, including materials science and organic synthesis.
