Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

459135

Sigma-Aldrich

Tetramethylammonium fluoride

97%

Sinonimo/i:

TMAF

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
(CH3)4NF
Numero CAS:
373-68-2
Peso molecolare:
93.14
Numero CE:
206-769-0
Numero MDL:
MFCD00011627
Codice UNSPSC:
12352116
ID PubChem:
24869514
NACRES:
NA.22

Saggio

97%

Forma fisica

solid

Punto di fusione

170 °C (dec.) (lit.)

Stringa SMILE

[F-].C[N+](C)(C)C

InChI

1S/C4H12N.FH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
GTDKXDWWMOMSFL-UHFFFAOYSA-M

Categorie correlate

Applicazioni

Reactant for:
  • Halide-induced ring opening of 2-substituted aziridinium salts
  • Synthesis of fluoro aromatics via fluorodenitration reactions
  • Synthesis of sevoflurane in ionic liquids by halogen-exchange fluorination
  • Synthesis of fluorinated Poly(oxomolybdates)
Tetramethylammonium fluoride may be used in combination with sulfuryl fluoride for the conversion of aryl phenols to aryl fluorides. It can react with aminosilanes to generate onium amide bases in situ, which can deprotonate heteroarenes.
Useful for halogen exchange.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302 + H312 + H332,H315,H319,H335

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 3

1 of 3

Tetrabutylammonium fluoride trihydrate technical, ≥90% (T)

Sigma-Aldrich

86843

Tetrabutylammonium fluoride trihydrate

Tris(trimethylsilyl)amine 98%

Sigma-Aldrich

360120

Tris(trimethylsilyl)amine

Tetramethylammonium chloride reagent grade, ≥98%

Sigma-Aldrich

T19526

Tetramethylammonium chloride

Nucleophilic deoxyfluorination of phenols via aryl Fluorosulfonate intermediates.
Schimler SD, et al.
Journal of the American Chemical Society, 139(4), 1452-1455 (2017)
Use of tetramethylammonium fluoride (TMAF) and alkali metal alkoxides as an activator for catalytic deprotonative functionalization of heteroaromatic C (sp2)?H bonds.
Inamoto K, et al.
Tetrahedron, 70(43), 7917-7922 (2014)
Martin-Louis Y Riu et al.
Science advances, 6(13), eaaz3168-eaaz3168 (2020-04-02)
This exploratory synthesis investigation was undertaken to determine the viability of replacing a single carbon vertex with another p-block element in a highly strained tetrahedrane molecule. Phosphorus was selected for this purpose because the stable molecular form of elemental phosphorus
Konrad Rykaczewski et al.
Langmuir : the ACS journal of surfaces and colloids, 29(3), 881-891 (2012-12-25)
The prospect of enhancing the condensation rate by decreasing the maximum drop departure diameter significantly below the capillary length through spontaneous drop motion has generated significant interest in condensation on superhydrophobic surfaces (SHS). The mobile coalescence leading to spontaneous drop
Yusuke Ide et al.
Chemical communications (Cambridge, England), 48(56), 7073-7075 (2012-06-12)
Hiroshima University Silicate-1 (HUS-1), composed of silicate sheets with a halved sodalite cage and the interlayer tetramethylammonium (TMA) cation in the cage, was modified with dimethyldichlorosilane to form the organic derivative in which a dimethyl group was grafted onto the
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.