≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Chlorotris(trimethylsilyl)silane is an organosilicon reagent, which is generally employed in the protection of alcohols. It is also used to prepare organometallic reagents, silyl enol ethers, and novel polymers/materials.
Application
Insertion into a P-P bond
Diastereoselective aldol and cascade reactions
Preparation of hypersilyl substituted monophosphines and diphosphines
| Pubchem Sid | 508811397 |
|---|---|
| Canonical Smiles | C[Si](C)(C)[Si]([Si](C)(C)C)([Si](C)(C)C)Cl |
| IUPAC Name | chloro-tris(trimethylsilyl)silane |
| InChIKey | HCOROOJWVHFMRJ-UHFFFAOYSA-N |
| INCHI | 1S/C9H27ClSi4/c1-11(2,3)14(10,12(4,5)6)13(7,8)9/h1-9H3 |
| Isomeric SMILES | C[Si](C)(C)[Si]([Si](C)(C)C)([Si](C)(C)C)Cl |
| WGK Germany | 3 |
| Molecular Weight | 283.11 |
| Reaxy-Rn | 2349885 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2349885&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organometallic compounds |
| Class | Organometalloid compounds |
| Subclass | Organosilicon compounds |
| Intermediate Tree Nodes | Organoheterosilanes |
| Direct Parent | Trialkylheterosilanes |
| Alternative Parents | Organic metalloid salts Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Trialkylheterosilane - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as trialkylheterosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one heteroatom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 K2230286 | Certificate of Analysis | Sep 02, 2026 | C153634 |
| C2626469 | Certificate of Analysis | Mar 21, 2026 | C153634 |
| C2626470 | Certificate of Analysis | Mar 21, 2026 | C153634 |
| E2410346 | Certificate of Analysis | Apr 25, 2024 | C153634 |
| E2410347 | Certificate of Analysis | Apr 25, 2024 | C153634 |
| E2410348 | Certificate of Analysis | Apr 25, 2024 | C153634 |
| K2230655 | Certificate of Analysis | Oct 20, 2022 | C153634 |
| Sensitivity | Moisture Sensitive;Heat sensitive |
|---|---|
| Flash Point(°F) | 87.8 °F |
| Flash Point(°C) | 31 °C |
| Boil Point(°C) | 93°C/1.8mmHg(lit.) |
| Melt Point(°C) | 46 °C |
| Molecular Weight | 283.100 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 3 |
| Exact Mass | 282.088 Da |
| Monoisotopic Mass | 282.088 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 170.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
