跳转至内容
Merck
CN

364533

三甲基氟硅烷

96%

别名:

Trimethylfluorosilane, 三甲基硅基氟化物

登录 查看组织和合同定价。

选择尺寸

关于此项目

线性分子式:
(CH3)3SiF
化学文摘社编号:
420-56-4
分子量:
92.19
EC Number:
206-997-0
UNSPSC Code:
12142100
PubChem Substance ID:
24862438
Beilstein/REAXYS Number:
1731132
MDL number:
MFCD00042064
Assay:
96%

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

InChI key

CTIKAHQFRQTTAY-UHFFFAOYSA-N

InChI

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

SMILES string

C[Si](C)(C)F

assay

96%

bp

16 °C (lit.)

mp

−74 °C (lit.)

density

0.793 g/mL at 25 °C (lit.)

Packaging

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:

Legal Information

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

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

存储类别

2A - Gases

wgk

WGK 3

flash_point_f

-22.0 °F - closed cup

flash_point_c

-30 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
13013AF
10816EO

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

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.
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
[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)
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
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持