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Butyltrichlorosilane

Catalog Number
ACM7521804
CAS Number
7521-80-4
Product Name
Butyltrichlorosilane
Structure
Category
Self-Assembly Materials; Silane Coupling Agents; POSS Nanohybrid Materials; Solution Deposition Precursors; Substrates and Electrode Materials
Description
Butyltrichlorosilane appears as a colorless liquid with a pungent odor. Flash point 126°F. Corrosive to metals and skin. Used to make various silicon containing compounds.
IUPAC Name
butyl(trichloro)silane
Molecular Weight
191.55g/mol
Molecular Formula
C4H9Cl3Si
Canonical SMILES
CCCC[Si](Cl)(Cl)Cl
InChI
InChI=1S/C4H9Cl3Si/c1-2-3-4-8(5,6)7/h2-4H2,1H3
InChI Key
FQEKAFQSVPLXON-UHFFFAOYSA-N
Boiling Point
288 °F at 760 mm Hg (USCG, 1999);148.5 °C;148.5 °C
Flash Point
126 °F (USCG, 1999);130 °F (54 °C) (open cup)
Density
1.16 at 68 °F (USCG, 1999);1.1606 g/cu cm at 20 C
Solubility
Soluble in ethyl ether, benzene, toluene, ethyl acetate;Soluble in heptane
Application
Butyltrichlorosilane is primarily used for surface modification and functionalization of materials. When applied to glass substrates, it introduces surface alkyl groups, which can effectively bind with specific compounds such as 2-methacryloyloxyethyl-4-azidobenzoate (MPAz), transforming hydrophobic glass surfaces into superhydrophilic ones. Additionally, it serves a crucial role in enhancing the sensitivity of zinc peroxide nanoparticle/polystyrene sulfonate hybrid-based sensors, improving their detection limit by three-fold. As a colorless liquid with a boiling point of 149℃ and notable reactivity, Butyltrichlorosilane significantly contributes to advancing material science and sensor technology applications.
Color/Form
Colorless liquid
Complexity
58.8
Corrosivity
Corrosive
Covalently-Bonded Unit Count
1
EC Number
231-381-3
Exact Mass
189.95391g/mol
Formal Charge
0
Heat of Vaporization
81 BTU/LB = 45 CAL/G = 1.9X10+5 JOULES/KG (EST)
Heavy Atom Count
8
Monoisotopic Mass
189.95391g/mol
NSC Number
93881
Other Experimental
Readily hydrolyzed with liberation of hydrogen chloride;Reacts with water or steam to produce heat and toxic and corrosive fumes;The reaction of organosilanes with halogens and halogen compounds usually proceeds in good yield through cleavage of the Si--H bond and formation of the silicon-halogen bond. Reaction with fluorine, however, does not proceed satisfactorily because of cleavage of not only the Si--H but also C--Si and C--H bonds. Direct halogenation with chlorination, bromine, and iodine proceeds smoothly, however. /Organosilanes/
Refractive Index
Index of refraction: 1.4363 at 25 °C/D
Rotatable Bond Count
2
UNII
ZQ9O7LYO00
UN Number
1747;1747;1747
Vapor Density
6.4 (Air = 1)
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