Iodotrimethylsilane
- CAS No.
- 16029-98-4
- Chemical Name:
- Iodotrimethylsilane
- Synonyms
- TRIMETHYLSILYL IODIDE;TMIS;TMS iodide;CT3610;IodotrimethyL;Trimethylsilyl io;Iodotrmethylsilane;trimethyiodosilane;Co-Formula CFS-710;iodotrimethyl-silan
- CBNumber:
- CB0478159
- Molecular Formula:
- C3H9ISi
- Molecular Weight:
- 200.09
- MDL Number:
- MFCD00001028
- MOL File:
- 16029-98-4.mol
- MSDS File:
- SDS
| Melting point | <0°C |
|---|---|
| Boiling point | 106 °C(lit.) |
| Density | 1.406 g/mL at 25 °C(lit.) |
| refractive index |
n |
| Flash point | −25 °F |
| storage temp. | -20°C |
| solubility | reacts |
| form | Liquid |
| color | Clear colorless to reddish |
| Specific Gravity | 1.47 |
| Water Solubility | reacts |
| Sensitive | Moisture & Light Sensitive |
| Hydrolytic Sensitivity | 8: reacts rapidly with moisture, water, protic solvents |
| BRN | 1731136 |
| Stability | Moisture Sensitive (Reactive) |
| InChIKey | CSRZQMIRAZTJOY-UHFFFAOYSA-N |
| CAS DataBase Reference | 16029-98-4(CAS DataBase Reference) |
| FDA UNII | 7A65KRZ6NV |
| NIST Chemistry Reference | Iodotrimethylsilane(16029-98-4) |
| EPA Substance Registry System | Silane, iodotrimethyl- (16029-98-4) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |   GHS02,GHS05 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H225-H314 | |||||||||
| Precautionary statements | P210-P233-P240-P280-P303+P361+P353-P305+P351+P338 | |||||||||
| Hazard Codes | F,C | |||||||||
| Risk Statements | 11-14-34 | |||||||||
| Safety Statements | 16-26-36/37/39-43-45-25 | |||||||||
| RIDADR | UN 2924 3/PG 2 | |||||||||
| WGK Germany | 3 | |||||||||
| F | 8-21 | |||||||||
| TSCA | Yes | |||||||||
| HazardClass | 3 | |||||||||
| PackingGroup | II | |||||||||
| HS Code | 29310095 | |||||||||
| NFPA 704 |
|
Iodotrimethylsilane price More Price(17)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 195529 | Iodotrimethylsilane 97% | 16029-98-4 | 5g | $48.8 | 2024-03-01 | Buy |
| Sigma-Aldrich | 195529 | Iodotrimethylsilane 97% | 16029-98-4 | 25g | $126 | 2024-03-01 | Buy |
| TCI Chemical | I0308 | Trimethylsilyl Iodide (stabilized with Aluminum) >95.0%(T) | 16029-98-4 | 5g | $33 | 2024-03-01 | Buy |
| TCI Chemical | I0308 | Trimethylsilyl Iodide (stabilized with Aluminum) >95.0%(T) | 16029-98-4 | 25g | $90 | 2024-03-01 | Buy |
| Alfa Aesar | A12902 | Iodotrimethylsilane, 97%, stab. with copper | 16029-98-4 | 5g | $45 | 2024-03-01 | Buy |
Iodotrimethylsilane Chemical Properties,Uses,Production
Chemical Properties
Straw liquid
Uses
Iodotrimethylsilane is used for the introduction of trimethylsilyl group in organic synthesis. It is also useful for gas chromatography analysis by converting alcohol into a silyl ether derivative, thereby making it more volatile than the original molecule.
Application
Iodotrimethylsilane can be used as a versatile reagent for the mild dealkylation of ethers, carboxylic esters, lactones, carbamates, acetals, phosphonate and phosphate esters; cleavage of epoxides, cyclopropyl ketones; conversion of vinyl phosphates to vinyl iodides; neutral nucleophilic reagent for halogen exchange reactions, carbonyl and conjugate addition reactions; use as a trimethylsilylating agent for formation of enol ethers, silyl imino esters, and N-silylenamines, alkyl, alkenyl and alkynyl silanes; Lewis acid catalyst for acetal formation, α- alkoxymethylation of ketones, for reactions of acetals with silyl enol ethers and allylsilanes; reducing agent for epoxides, enediones, α-ketols, sulfoxides, and sulfonyl halides; dehydrating agent for oximes.
Preparation
Iodotrimethylsilane is prepared by mixing equimolar amounts of chlorotrimethylsilane and sodium iodide in acetonitrile, reduces various benzylic alcohols to the corresponding phenylalkanes. Other have been reported for the preparation of Trimethylsilyl Iodide(TMS-I): chlorotrimethylsilane undergoes halogen exchange with either lithium iodide in CHCl3 or sodium iodide in MeCN, which allows in situ reagent formation. Alternatively, hexamethyldisilane reacts with iodine at 25–61°C to afford TMS-I with no byproducts.
Reactions
Trimethylsilyl iodide reacts under mild conditions in the absence of a catalyst with alkyl fluorides as well as with benzyl and tertiary alkyl chlorides and bromides to give good yields of alkyl iodides and the corresponding trimethylsilyl halides.
General Description
Iodotrimethylsilane is a multipurpose reagent used in various organic reactions. It is used for the dealkylation of few compounds like lactones, ethers, acetals, and carbamates and trimethylsilylating agent for the synthesis of silyl imino esters, alkyl and alkenyl silanes, etc. It also acts as a Lewis acid catalyst and as a reducing agent in many organic reactions.
Synthesis
This procedure describes a convenient method for the preparation of Iodotrimethylsilane: A 250-ml., two-necked, round-bottomed flask equipped with a magnetic stirring bar, an addition funnel for solids, and a reflux condenser bearing a nitrogen inlet is charged with 5.6 g. (0.21 mole) of aluminum powder and 16.2 g. (0.100 mole) of hexamethyldisiloxane and purged with nitrogen. The mixture is stirred and heated with an oil bath at 60°C as 50.8 g. (0.200 mole) of iodine is added slowly through the addition funnel over 55 minutes. The bath temperature is raised to ca. 140°C, and the mixture is heated under reflux for 1.5 hours. The reflux condenser is removed, and the flask is equipped for distillation at atmospheric pressure. The bath temperature is gradually raised from 140°C to 210°C, and the clear, colorless distillate is collected, yielding 32.6–35.3 g. (82–88%) of iodotrimethylsilane, b.p. 106–109°C.
Purification Methods
Add a little antimony powder and fractionate with this powder in the still. 20 1.470. Stabilise the distillate with 1% wt of Cu powder. [Eaborn J Chem Soc 3077 1950, Beilstein 4 IV 4009.]
Iodotrimethylsilane Preparation Products And Raw materials
Raw materials
Preparation Products
1of3
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| TCI AMERICA | 800-4238616 | sales@tciamerica.com | Americas | 23653 | 75 |
| Hebei Chuanghai Biotechnology Co,.LTD | +86-13131129325 | sales1@chuanghaibio.com | China | 5893 | 58 |
| Hebei Kingfiner Technology Development Co.Ltd | +86-15532196582 +86-15373005021 | lisa@kingfinertech.com | China | 3010 | 58 |
| Capot Chemical Co.,Ltd. | +86-（0）57185586718 +86-13336195806 | sales@capot.com | China | 29791 | 60 |
| Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 | info@dakenam.com | China | 18779 | 58 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21634 | 55 |
| Shanghai Time Chemicals CO., Ltd. | +86-021-57951555 +8617317452075 | jack.li@time-chemicals.com | China | 1803 | 55 |
| ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32957 | 60 |
| career henan chemical co | +86-0371-86658258 +8613203830695 | sales@coreychem.com | China | 29884 | 58 |
| Win-Win Chemical CO., Limited | 0086-577-64498589 | sales@win-winchemical.com | CHINA | 998 | 58 |
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View Lastest Price from Iodotrimethylsilane manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2024-11-18 | Trimethylsilyl Iodide
16029-98-4
|
US $1450.00 / Kg | 0.100Kg | 98 | 500 Kg | R&D Scientific Inc. | |
 |
2024-10-11 | Iodotrimethylsilane
16029-98-4
|
US $100.00-50.00 / KG | 1KG | 99% | 10000kg | Hebei Chuanghai Biotechnology Co,.LTD | |
 |
2024-06-14 | Iodotrimethylsilane
16029-98-4
|
US $0.00-0.00 / kg | 1kg | 0.99 | 50000kg | Hebei Kingfiner Technology Development Co.Ltd |
-
- Trimethylsilyl Iodide
16029-98-4
- US $1450.00 / Kg
- 98
- R&D Scientific Inc.
-
- Iodotrimethylsilane
16029-98-4
- US $100.00-50.00 / KG
- 99%
- Hebei Chuanghai Biotechnology Co,.LTD
-
- Iodotrimethylsilane
16029-98-4
- US $0.00-0.00 / kg
- 0.99
- Hebei Kingfiner Technology Development Co.Ltd