Ordering
Available Variants5 mL
CHA.38967-5mL
Price
€96.80
Available – Dispatch in 14 days
25 mL
CHA.38967-25mL
Price
€238.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mL | CHA.38967-5mL | €96.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mL | CHA.38967-25mL | €238.20 |
≥99.0% (GC)
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)3SiCH2I |
|---|---|
| CAS Number | 4206-67-1 |
| Molecular Weight | 214.12 |
| UNSPSC Code | 12352103 |
| NACRES | NA.22 |
| PubChem Substance ID | 24880966 |
| EC Number | 224-123-6 |
| Beilstein/REAXYS Number | 1731485 |
| MDL number | MFCD00001077 |
Safety Information Handling visibility
| pictograms |
GHS02
GHS07
  GHS02,GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H226,H315,H319,H335 |
| pcodes | P210 - P233 - P240 - P241 - P303 + P361 + P353 - 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 | 84.2 °F - closed cup |
| flash_point_c | 29 °C - closed cup |
| ppe | Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(Iodomethyl)trimethylsilane, with the CAS number 4206-67-1, is a chemical compound that has been utilized in various organic synthesis reactions. This reagent is particularly useful for introducing methyl groups into molecules, taking advantage of its iodine moiety to facilitate substitution reactions. Its trimethylsilyl group provides stability and solubility, making it a versatile intermediate in the synthesis of complex molecules. The compounds reactivity is influenced by its molecular structure, which allows it to participate in a range of chemical transformations, including cross-coupling reactions and nucleophilic substitutions. As a result, (iodomethyl)trimethylsilane has found applications in the synthesis of pharmaceuticals, agrochemicals, and materials science, highlighting its importance as a building block in modern organic chemistry. Its properties and reactivity profile make it a valuable tool for chemists seeking to construct complex molecular architectures.
