Trimethylsilylacetylen

Trimethylsilylacetylene

HCID 66111CAS 1066-54-2

Grundinformationen

Standard-SMILES
C#C[Si](C)(C)C
InChIKey
CWMFRHBXRUITQE-UHFFFAOYSA-N
Summenformel
C5H10Si
Durchschnittliche Molmasse
98,22 g/mol
Monoisotopische Masse
98,05517685

Namen und Bezeichner

Bevorzugter Name
Trimethylsilylacetylene
IUPAC
ethynyl(trimethyl)silane
Lokaler Name
Trimethylsilylacetylen
Englischer Name
Trimethylsilylacetylene
Summenformel
C5H10Si
Molmasse
98.22

Namen und Synonyme

EthynyltrimethylsilaneTrimethylsilylacetylene1066-54-2(Trimethylsilyl)acetyleneethynyl(trimethyl)silaneethynyl-trimethyl-silaneSilane, ethynyltrimethyl-trimethylsilyl acetylenetrimethylsilylethyne(Trimethylsilyl)ethyneTMS acetyleneTMS-acetylene
Weitere Namen anzeigen
TMSAETHINYLTRIMETHYLSILANE1-TrimethylsilylethyneThimethylsilylacetylene(Thrimethylsilyl)acetylene
C5H10SiMFCD00008569(Trimethylsilyl)acetylene-dTrimethylethynylsilaneethynyltrimethyl silanetrimethylsilyl-acetylene1-(Trimethylsilyl)acetylenetms-acetylide

Datenbank-Bezeichner

CAS
1066-54-2、7299-46-9
PubChem CID
66111
DTXSID
DTXSID7061435
EC Number
213-919-9、685-813-4
Nikkaji
J209.060K

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
0 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
0
Frei drehbare Bindungen
1
Schwere Atome
6

Experimentelle und physikochemische Eigenschaften

Chemical ClassesMetals -> Metalloid Compounds (Silicon)
SpringerMaterials Properties29Si nuclear magnetic resonance spectrum
Vapor Pressure224.0 [mmHg]
Physical DescriptionColorless liquid; [Alfa Aesar MSDS]

Physikochemische Eigenschaften

Schmelzpunkt
0 °C · >0°C
Siedepunkt
53 °C · 53 °C(lit.)
Dichte
0.695 g/mL · 0.695 g/mL at 25 °C(lit.)
Dampfdruck
4.18 psi · 4.18 psi ( 20 °C)
Brechungsindex
20 · n20/D 1.388(lit.)
Flammpunkt
30 °F · <−30 °F

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H225 (72.1%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 86 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

Gefahrenhinweise

Regulatory Information · 2 Einträge

Status: Active Update: 02-06-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/33552

Trimethylsilylacetylene: HSNO Approval: HSR006727 Approved with controls

Hazards SummaryMay cause irritation; [Alfa Aesar MSDS] See 1-Phenyl-2-(trimethylsilyl)acetylene and Phenylacetylene.
Hazard Classes and Categories · 2 Einträge

Flam. Liq. 2 (72.1%)

Flam. Liq. 2 (100%)

CSL Reaction Information · 6 Einträge

CSL00196

(Trimethylsilyl)acetylene + Acetone + Oxygen

"We would like to report an explosion that occurred in our laboratory last year while performing an oxidative coupling of trimethylsilylacetylene (TMSA) in a Glaser-Hay reaction. The explosion ruptured the 2-L reaction flask and seriously injured a researcher. This reaction has been routinely used in our and many other laboratories to prepare 1,4-bis(trimethylsilyl)butadiyne-1,3 on a large scale (>100 g), and no dangerous or unusual behavior was previously noted. The procedure involves purging oxygen through a solution of TMSA in acetone in the presence of a copper(I) chloride:tetramethylethylenediamine complex catalyst at room temperature as described by Andrew B. Holmes et al. (Org. Syntheses 1993, Coll. Vol. 8, 63). The authors of the procedure recommend a safety shield as a general precaution while working with flammable materials in the atmosphere of oxygen, although no hazard was ever encountered. In this incident, the explosion occurred as soon as we started adding the solution of catalyst in acetone to the reaction. We have consulted with the pioneer of this reaction (Allan S. Hay) and the submitting author of the procedure (Holmes) and considered various scenarios to explain the explosion. Ignition of acetone/TMSA vapor by the external sources was hardly possible as the flask was well sealed and the outgoing gases were passed through a dry-ice condenser (lowering the vapor pressure below the explosive concentration) and brought to the back side of the fume hood through a 1-meter hose. The reaction temperature (5 ºC) was noted by the researcher a few seconds before the explosion, thus ruling out unexpected reaction exothermy. The autoignition of the vapor on a hot stirring adapter (possibly heated by rotation-induced friction) was refuted, because joint lubrication was checked before setting up the experiment, and it would have required achieving an unrealistic temperature of greater than 300 ºC. Also, the explosion occurred upon adding the first few drops of copper catalyst, which makes crystallization of the explosive intermediate—copper bis(trimethylsilylacetylide)—highly improbable. We speculate that a discharge of static electricity between the syringe needle and the digital thermometer inside the flask is the most likely cause of this explosion. A digital thermometer connected to a stirring hot plate (IKA) was used in the reaction, and a plastic syringe with a long metal needle was introduced through the same neck. An induced static voltage on the syringe through friction from handling (often observed in Montreal winter indoors while walking or even simply sitting) could then cause a sufficient differential potential on the needle for a discharge spark to occur close to the metallic body of the digital thermometer. The oxygen-rich atmosphere lowers the ignition energy and makes even a weak spark sufficient to cause a fire. The incident emphasizes once more the potential danger of mixing oxygen gas with flammable solvents or reagents. More important, introducing two conductors into a flask brings a risk of static electricity discharge between the conductors, which is dangerous whenever a flammable solvent is used without inert gas. As wired metal-gauge digital thermometers are used more often in synthetic practice, precautions must be taken to avoid their contact with other metallic (conducting) parts inside the reaction flasks." (reprint of the full-text)

Explosive

Large (>100g)

Oxidation

Sicherheitsdaten

wgk
-
tsca
TSCA listed
ridadr
UN 1993 3/PG 2
hs_code
29310095
risk_code
11-36/37/38
hazard_code
F,Xi

Chemie und Industrie

Verwendung und Herstellung

General Manufacturing InformationSilane, ethynyltrimethyl-: ACTIVE
Anwendungen · 1 Eintrag

VerwendenTrimethylsilylacetylene is a valuable reagent used in ethynylation by palladium(0)-catalyzed coupling/condensation with aryl and vinyl halides and triflates, or by nucleophilic attack of the corresponding acetylide on electrophilic centers; reacts with alkyl iodides, tin hydrides,6 and dichloroketene in a regioselective and stereoselective manner, participating in the following synthesis reactions: Ethynylations, Palladium(0)-Catalyzed Coupling Reactions,Reaction of Trimethylsilylacetylides with Electrophiles, Radical-Initiated and Transition Metal-Catalyzed Additions, Cycloaddition Reactions, Ethynylations, Cycloaddition Reactions, Further Transformations etc.

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