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Sigma-Aldrich

Fluorotrimethylsilane

96%

Sinônimo(s):

Trimethylfluorosilane, Trimethylsilyl fluoride

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About This Item

Fórmula linear:
(CH3)3SiF
Número CAS:
420-56-4
Peso molecular:
92.19
Beilstein:
1731132
Número CE:
206-997-0
Número MDL:
MFCD00042064
Código UNSPSC:
12142100
ID de substância PubChem:
24862438

Ensaio

96%

pb

16 °C (lit.)

pf

−74 °C (lit.)

densidade

0.793 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C[Si](C)(C)F

InChI

1S/C3H9FSi/c1-5(2,3)4/h1-3H3

chave InChI

CTIKAHQFRQTTAY-UHFFFAOYSA-N

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Embalagem

Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

Informações legais

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

espiga da mangueira

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Z146811

Hose adapter, brass

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Palavra indicadora

Danger

Frases de perigo

H224,H280,H315,H319,H335

Classificações de perigo

Eye Irrit. 2 - Flam. Liq. 1 - Press. Gas Compr. Gas - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

2A - Gases

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

-22.0 °F - closed cup

Ponto de fulgor (°C)

-30 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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L G Hutchins et al.
The International journal of applied radiation and isotopes, 36(5), 375-378 (1985-05-01)
18F-Labeled fluorotrimethylsilane was prepared by nucleophilic substitution of chlorotrimethylsilane with reactor produced [18F]fluoride. Hydrolysis of fluorotrimethylsilane by aqueous tetraethylammonium hydroxide followed by removal of water with a mechanical pump gave a powerful source of no carrier added nucleophilic 18F. Reaction
M S Rosenthal et al.
The International journal of applied radiation and isotopes, 36(4), 318-319 (1985-04-01)
[18F]Fluorotrimethylsilane was prepared in 80% decay corrected yield by reaction of no-carrier added tetramethyl-ammonium fluoride (hydroxide as bulk anion) with chlorotrimethylsilane in 65% aqueous acetonitrile. The 18F gas was collected in a cold-trap at -130 degrees C and found to
L Gámiz-Gracia et al.
Journal of pharmaceutical and biomedical analysis, 22(6), 909-913 (2000-06-17)
A selective dynamic method for the determination of fluoride in pharmaceuticals based on the integration of pervaporation and potentiometric detection in a laboratory-made module is proposed. The analyte was continuously converted into volatile trimetylfluorosilane by reaction with hexamethyldisilazane, injected into
S J Gatley
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 40(6), 541-544 (1989-01-01)
A flow-through system is described for rapid purification of [18F]fluoride for nucleophilic substitution reactions. It depends on generation of [18F]fluorotrimethylsilane from aqueous 18F solutions and subsequent collection of the gas and its hydrolysis by base in near anhydrous acetonitrile. Potassium
Ian H Krouse et al.
Journal of the American Society for Mass Spectrometry, 16(5), 697-707 (2005-05-03)
In this study, preparation and decomposition of five novel pentavalent fluorosiliconates, RSi(CH3)3F- (R = CH3CH2O, CF3CH2O, (CH3)2CHO, (CH3)3SiO, and (CH3)3SiNH) is used to investigate the process of fluoride-induced desilylation. The siliconates were characterized by collision-induced dissociation and energy-resolved mass spectrometry.
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