high quality Pentyltrichlorosilane 99% transparent liquid KANBEI

Trichloropentylsilane

Silane,trichloropentyl-;Trichloropentylsilane;Amyltrichlorosilane;Pentylsilicon trichloride;Trichloroamylsilane;Pentyltrichlorosilane;n-Pentyltrichlorosilane

107-72-2

C5H11Cl3Si

InChIKey=KWDQAHIRKOXFAV-UHFFFAOYSA-N

205.59

205.59

203-515-0

N9GP7288ZP

1728

COLORLESS TO YELLOW LIQUID

2931900090

Silane Reagent

0

6.32

Amyltrichlorosilane appears as a colorless to yellow liquid with a pungent odor. It is combustible and has a flash point of 145°F. Corrosive to metals and tissue.

1.1330 g/cm³ @ Temp: 20 °C

-30 °C

172 °C

30°C

1.448

All containers, pipes, apparatus, installations, and structures used for manufacture, storage, transport, or use of these substances must be of material resistant to corrosive substances or be protected by suitable coatings ... All containers or receptacles should be clearly labelled to indicate their contents and should bear the danger symbol for corrosives. /Corrosive substances/

Lower explosive limit: 3.4%; Upper explosive limit: > or = 9.5%

SHARP, LIKE HYDROCHLORIC ACID; PUNGENT

A MIXTURE OF ISOMERS|Readily hydrolzed by moisture with the liberation of hydrogen chloride.|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/

Reacts with water to form hydrogen chloride (hydrochloric acid). Amyltrichlorosilane reacts with water to generate gaseous HCl. Based on a scenario where the chemical is spilled into an excess of water (at least 5 fold excess of water), half of the maximum theoretical yield of Hydrogen Chloride gas will be created in 3.2 minutes. After mixing particular chemicals into water, there may be a delay of <1-10 minutes before gas generation may be observed. For this chemical, a 27 second induction time was observed. Experimental details are in the following: "Development of the Table of Initial Isolation and Protective Distances for the 2008 Emergency Response Guidebook", ANL/DIS-09-2, D.F. Brown, H.M. Hartmann, W.A. Freeman, and W.D. Haney, Argonne National Laboratory, Argonne, Illinois, June 2009.

Chlorosilanes

Water-Reactive

Chlorosilanes, such as AMYLTRICHLOROSILANE, are compounds in which silicon is bonded to from one to four chlorine atoms with other bonds to hydrogen and/or alkyl groups. Chlorosilanes react with water, moist air, or steam to produce heat and toxic, corrosive fumes of hydrogen chloride. They may also produce flammable gaseous H2. They can serve as chlorination agents. Chlorosilanes react vigorously with both organic and inorganic acids and with bases to generate toxic or flammable gases.

-6,630 BTU/LB = -3,680 CAL/G = -154X10+5 J/Kg (EST)

Corrodes metals

86.8 BTU/LB = 48.2 CAL/G = 2.02X10+5 J/KG (EST)