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Available Variants5 mL
CHA.90531-5mL
Price
€207.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mL | CHA.90531-5mL | €207.20 |
≥98.0% (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
| Empirical Formula (Hill Notation) | C4H13NSi |
|---|---|
| CAS Number | 18166-02-4 |
| Molecular Weight | 103.24 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 57653491 |
| EC Number | 242-049-2 |
| Beilstein/REAXYS Number | 1731488 |
| MDL number | MFCD00042931 |
| Assay | ≥98.0% (GC) |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS02
GHS05
  GHS02,GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H225,H314 |
| pcodes | P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338 |
| Hazard Classifications | Flam. Liq. 2 - Skin Corr. 1B |
| Storage Class | 3 - Flammable liquids |
| wgk | WGK 3 |
| flash_point_f | 48.2 °F - closed cup |
| flash_point_c | 9 °C - closed cup |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(Trimethylsilyl)methylamine, with the CAS registry number 18166-02-4, is a chemical compound that has garnered significant attention in various fields of research. This organosilicon compound is characterized by the presence of a trimethylsilyl group attached to a methylamine moiety. As a result, it exhibits unique properties that make it a valuable reagent in organic synthesis. The compounds reactivity is influenced by the steric and electronic effects of the trimethylsilyl group, which can participate in various reactions, including nucleophilic substitutions and additions. Furthermore, (trimethylsilyl)methylamine has been employed as a building block in the synthesis of complex molecules, including pharmaceuticals and materials. Its versatility and potential applications have sparked interest among chemists, who continue to explore its properties and uses in diverse areas of research.
