추천 제품
분석
96%
bp
16 °C (lit.)
mp
−74 °C (lit.)
density
0.793 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(C)F
InChI
1S/C3H9FSi/c1-5(2,3)4/h1-3H3
InChI key
CTIKAHQFRQTTAY-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
포장
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:
법적 정보
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
또한 이 제품과 함께 일반적으로 구입
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제품 번호
설명
가격
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 1 - Press. Gas Compr. Gas - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
2A - Gases
WGK
WGK 3
Flash Point (°F)
-22.0 °F - closed cup
Flash Point (°C)
-30 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
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
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
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
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
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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