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化驗
96%
bp
16 °C (lit.)
mp
−74 °C (lit.)
密度
0.793 g/mL at 25 °C (lit.)
SMILES 字串
C[Si](C)(C)F
InChI
1S/C3H9FSi/c1-5(2,3)4/h1-3H3
InChI 密鑰
CTIKAHQFRQTTAY-UHFFFAOYSA-N
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包裝
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:
Compatible with the following:
法律資訊
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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軟管倒鉤
产品编号
说明
价格
訊號詞
Danger
危險分類
Eye Irrit. 2 - Flam. Liq. 1 - Press. Gas Compr. Gas - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
2A - Gases
水污染物質分類（WGK）
WGK 3
閃點（°F）
-22.0 °F - closed cup
閃點（°C）
-30 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves
其他客户在看
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.
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
[Gas chromatographic fluoride determination following adsorption of trimethylfluorsilane on Porapak P].
K Seifert
Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete, 29(2), 80-80 (1983-02-01)
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
P Venkateswarlu
Analytical chemistry, 64(4), 346-349 (1992-02-15)
The conventional procedure for separation of fluoride as trimethylfluorosilane in Conway diffusion cells involves the use of grease for sealing the cell and also for closing the hole in the lid drilled for introduction of hexamethyldisiloxane. We have developed a
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