CAS 3768-58-9
:N,N,N′,N′,1,1-Hexamethylsilanediamin
Beschreibung:
N,N,N′,N′,1,1-Hexamethylsilanediamin, mit der CAS-Nummer 3768-58-9, ist eine organosiliciumverbindung, die durch die Anwesenheit von Siliziumatomen, die an Stickstoff und Kohlenstoff gebunden sind, gekennzeichnet ist. Diese Verbindung weist ein zentrales Siliziumatom auf, das von sechs Methylgruppen und zwei aminischen funktionellen Gruppen umgeben ist, die zu ihren einzigartigen chemischen Eigenschaften beitragen. Es ist typischerweise eine farblose bis blassgelbe Flüssigkeit bei Raumtemperatur und zeigt eine relativ niedrige Viskosität. Die Anwesenheit von Aminogruppen ermöglicht eine potenzielle Reaktivität in verschiedenen chemischen Reaktionen, einschließlich solcher, die nucleophile Substitution und Koordination mit Metallionen betreffen. Darüber hinaus verbessern die Methylgruppen seine hydrophoben Eigenschaften, wodurch es weniger löslich in Wasser, aber besser mit organischen Lösungsmitteln kompatibel ist. N,N,N′,N′,1,1-Hexamethylsilanediamin wird häufig in der Synthese von silanbasierten Materialien und als Kopplungsagent in der Polymerchemie verwendet. Seine einzigartige Struktur und Eigenschaften machen es in verschiedenen industriellen Anwendungen wertvoll, insbesondere in den Bereichen Materialwissenschaften und Oberflächenmodifikation.
Formel:C6H18N2Si
InChl:InChI=1S/C6H18N2Si/c1-7(2)9(5,6)8(3)4/h1-6H3
InChI Key:InChIKey=QULMGWCCKILBTO-UHFFFAOYSA-N
SMILES:[Si](N(C)C)(N(C)C)(C)C
Synonyme:- Bdmads
- Bis(N,N-dimethylamino)dimethylsilane
- Dimethylbis(dimethylamino)silane
- Dimethyldi(N,N-dimethylamino)silane
- Dimethylsilylbis(dimethylamine)
- Hexamethylsilanediamine
- Ls 1440
- N,N,N',N',1,1-Hexamethylsilanediamine
- Silanediamine, hexamethyl-
- [(Dimethylamino)dimethylsilyl]dimethylamine
- silanediamine, N,N,N',N',1,1-hexamethyl-
- Weitere Synonyme anzeigen
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8 Produkte.
Bis(dimethylamino)dimethylsilane
CAS:Formel:C6H18N2SiReinheit:>97.0%(GC)Farbe und Form:Colorless to Almost colorless clear liquidMolekulargewicht:146.31Bis(dimethylamino)dimethylsilane, 97%
CAS:<p>Bis(dimethylamino)-dimethyl silane has been used to silanize pH-sensitive microelectrodes, used to measure the membrane potential in oocytes, in an experimental procedure aimed towards cloning and characterizing human electrogenic Na+-cotransporter isoform (hhNBC). It is also used for microelectrode</p>Formel:C6H18N2SiReinheit:97%Farbe und Form:Clear colorless, LiquidMolekulargewicht:146.31Bis(dimethylamino)dimethylsilane, 99+% BDMADMS
CAS:<p>Bis(dimethylamino)dimethylsilane, 99+% BDMADMS</p>Formel:N(CH3)2(CH3)2SiReinheit:99+%Farbe und Form:colorless liq.Molekulargewicht:146.31N,N,N′,N′,1,1-Hexamethylsilanediamine
CAS:Formel:C6H18N2SiFarbe und Form:LiquidMolekulargewicht:146.3060Bis(dimethylamino)dimethylsilane
CAS:<p>S01600 - Bis(dimethylamino)dimethylsilane</p>Formel:C6H18N2SiReinheit:>95%Farbe und Form:LiquidMolekulargewicht:146.309Bis(dimethylamino)dimethylsilane
CAS:<p>Bis(dimethylamino)dimethylsilane</p>Reinheit:95%Molekulargewicht:146.31g/molRef: 54-OR928817
1mlNachfragen25gNachfragen5mlNachfragen100gNachfragen25mlNachfragen100mlNachfragen500mlNachfragenBIS(DIMETHYLAMINO)DIMETHYLSILANE
CAS:<p>Bridging Silicon-Based Blocking Agent<br>Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.<br>ALD Material<br>Atomic layer deposition (ALD) is a chemically self-limiting deposition technique that is based on the sequential use of a gaseous chemical process. A thin film (as fine as -0.1 Å per cycle) results from repeating the deposition sequence as many times as needed to reach a certain thickness. The major characteristic of the films is the resulting conformality and the controlled deposition manner. Precursor selection is key in ALD processes, namely finding molecules which will have enough reactivity to produce the desired films yet are stable enough to be handled and safely delivered to the reaction chamber.<br>Alkyl Silane - Conventional Surface Bonding<br>Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.<br>Bis(Dimethylamino)dimethylsilane; Dimethylbis(dimethylamino)silane; Hexamethylsilanediamine; DMS<br>More reactive than SIB4120.0Couples silanol terminated siloxanesReacted with diols, diamines, and treatment for glassSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure<br></p>Formel:C6H18N2SiReinheit:97%Farbe und Form:Straw LiquidMolekulargewicht:146.31Bis(dimethylamino)dimethylsilane
CAS:<p>Bis(dimethylamino)dimethylsilane (Bis-DMAS) is a silylating agent that reacts with the hydroxy groups of siloxanes to form a cross-link. It can be used as a functional group for the synthesis of polymers, coatings, and adhesives. Bis-DMAS has also been used to improve the reactivity of other functional groups, such as carbonyls, amines, nitriles, and epoxides. It is reactive in air and moisture and should be stored in an inert atmosphere. Bis-DMAS reacts with metal surfaces to form a coating by reacting with both the metal surface and hydrogen atoms on the surface. The reaction temperature is dependent on the substrate: higher temperatures are needed for copper than aluminum due to copper's higher reactivity. The activation energies are different for each reaction type: thermal reactions have an activation energy of 40 kJ/mol while electrochemical reactions have an activation energy of</p>Formel:C6H18N2SiReinheit:Min. 95%Molekulargewicht:146.31 g/mol







