268097
Tetrabutilammonio fosfato
97%
Sinonimo/i:
Tetrabutilammonio diidrogeno fosfato
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Formula condensata:
(CH3CH2CH2CH2)4N[OP(OH)2O]
Numero CAS:
Peso molecolare:
339.45
Beilstein:
5196532
Numero CE:
Numero MDL:
Codice UNSPSC:
12352103
Prodotti consigliati
![1,4-Diazabicyclo[2.2.2]octane ReagentPlus®, ≥99%](/deepweb/assets/sigmaaldrich/product/structures/366/129/a6ff4175-974d-4fac-9038-b35e508ef252/640/a6ff4175-974d-4fac-9038-b35e508ef252.png)
![1,4-Diazabicyclo[2.2.2]octane for synthesis](/deepweb/assets/sigmaaldrich/product/images/488/587/f5a877b3-e573-4686-931f-648015f4d284/640/f5a877b3-e573-4686-931f-648015f4d284.jpg)
Saggio
97%
Punto di fusione
151-154 °C (lit.)
Stringa SMILE
OP(O)([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/C16H36N.H3O4P/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-5(2,3)4/h5-16H2,1-4H3;(H3,1,2,3,4)/q+1;/p-1
ARRNBPCNZJXHRJ-UHFFFAOYSA-M
Cerchi prodotti simili? Visita Guida al confronto tra prodotti
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
![Soluzione di tetra-n-butilammonio idrossido in 2-propanol/methanol for titrations in nonaqueous media c[(C4H9)4NOH] = 0.1 mol/l (0.1 N), Titripur®, reag. USP](/deepweb/assets/sigmaaldrich/product/images/217/795/18cba546-7592-4bb4-8b67-0b4b229e0a2f/640/18cba546-7592-4bb4-8b67-0b4b229e0a2f.jpg)
Pieter van Dillewijn et al.
Applied and environmental microbiology, 74(21), 6820-6823 (2008-09-16)
Homogenous preparations of XenB of Pseudomonas putida, pentaerythritol tetranitrate reductase of Enterobacter cloacae, and N-ethylmaleimide reductase of Escherichia coli, all type II hydride transferases of the Old Yellow Enzyme family of flavoproteins, are shown to reduce the polynitroaromatic compound 2,4,6-trinitrotoluene
Erbo Shi et al.
Organic letters, 14(13), 3384-3387 (2012-06-27)
A metal-free C-H oxidation for the construction of allylic esters has been developed. The use of a commercially available and inexpensive catalyst and oxidant, and readily available starting materials, coupled with the operational simplicity of the reaction, renders the methodology
Fabio Galeotti et al.
Journal of chromatography. A, 1284, 141-147 (2013-03-05)
In this study, by using tetrabutylammonium bisulfate as ion-pairing reagent, we were able to separate all the main heparin/heparan sulfate disaccharides generated by the action of heparinases along with the main Hep tetrasaccharide possessing a 3-O-sulfate group on the sulfoglucosamine
R Bryan Sears et al.
Journal of inorganic biochemistry, 121, 77-87 (2013-01-29)
The complex cis-[Ru(phpy)(phen)(CH3CN)2](+) (phpy=2-phenylpyridine, phen=1,10-phenanthroline) was investigated as a potential photodynamic therapy (PDT) agent. This complex presents desirable photochemical characteristics including a low energy absorption tail extending into the PDT window (600-850nm) and photoinduced exchange of the CH3CN ligands, generating
Morteza Moradi et al.
The Analyst, 137(15), 3549-3557 (2012-06-27)
Hollow fiber-based liquid phase microextraction (HF-LPME) using conventional solvents is limited by their relative instability and high volatility. The use of supramolecular solvents as a liquid membrane phase could overcome these inconveniences due to their negligible vapour pressure and high
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.