- Product Name:
- Silane, phenyltrichloro-
- Silane, trichlorophenyl-
- Silicon phenyl trichloride
- Product Categories:
- organosilicon compounds
- Functional Materials
- Si (Classes of Silicon Compounds)
- Si-Cl Compounds
- Silane Coupling Agents
- Silane Coupling Agents (Intermediates)
- Phenyl Silanes
- Mol File:
Phenyltrichlorosilane Chemical Properties
- Melting point:
- Boiling point:
- 201 °C(lit.)
- 1.321 g/mL at 25 °C(lit.)
- vapor pressure
- 44.3Pa at 20℃
- refractive index
- n20/D 1.523(lit.)
- Flash point:
- 196 °F
- soluble in Chloroform,Benzene,Ether
- Specific Gravity
- explosive limit
- Water Solubility
- Moisture Sensitive
- Hydrolytic Sensitivity
- 8: reacts rapidly with moisture, water, protic solvents
- CAS DataBase Reference
- 98-13-5(CAS DataBase Reference)
- NIST Chemistry Reference
- Phenyl trichlorosilane(98-13-5)
- EPA Substance Registry System
- Trichlorophenylsilane (98-13-5)
- Hazard Codes
- Risk Statements
- Safety Statements
- UN 1804 8/PG 2
- WGK Germany
- HS Code
- Hazardous Substances Data
- 98-13-5(Hazardous Substances Data)
- LD50 orl-rat: 2390 mg/kg AMIHBC 10,61,54
Phenyltrichlorosilane Usage And Synthesis
Phenyl trichlorosilane is a colorless to light yellow liquid.
Phenyltrichlorosilane can be used in the development of high-capacitance polymer dielectric for low-voltage organic transistors.
The high-temperature condensation (HTC) technique proved to be very convenient and economical for the production of phenyltrichlorosilane and in recent years has become one of the main industrial techniques for its synthesis.
The synthesis of phenyltrichlorosilane by HTC technique is conducted according to the reaction:
HSiCI3 + C6H5CI →（HCI）→ C6H5SiCI3
In this case, similarly to the vinyltrichlorosilane case, in the conditions of synthesis (600-640 °C) there is a secondary reaction of reduction, which forms silicon tetrachloride and benzene. However, if the process is conducted in the presence of an initiator (5% of diazomethane), it is possible to reduce the temperature down to 500-550 °C. Then the secondary reaction proceeds very slowly, which increases the yield of phenyltrichlorosilane by 1.5 times. To suppress the reduction process, one can also add benzene and silicon tetrachloride into the reactive mixture. It is also possible to boost the yield of phenyltrichlorosilane and increase the degree of the chlorobenzene transformation by using two subsequent reactors.
A colorless liquid with a pungent odor. Flash point 91°F. Decomposed by moisture or water to hydrochloric acid with evolution of heat. Corrosive to metals and tissue.
Chlorosilanes, such as Phenyltrichlorosilane 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.
Highly toxic; may cause death or permanent injury after short inhalation exposure to small quantity. Chemical burns to all exposed membranes and tissues with severe tissue destruction. Inhalation -- lungs may fill up with fluid or throat may swell causing suffocation. Eyes -- damage to corneas may cause blindness. Delayed: after oral exposure stomach and intestines may perforate or be obstructed by scar tissue.
Flammability and Explosibility
Phenyl trichlorosilane is used to make silicones for water repellants, insulating resins; heat resistant paints; and as a laboratory reagent
UN1804 Phenyltrichlorosilane, Hazard class: 8; Labels: 8-Corrosive material.
- 010-82848833 400-666-7788
- PHENYLSELENENYL CHLORIDE
- Phenyltrichlorosilane,phenylmethyldichlorosilane polymer,Phenyltrichlorosilane, phenylmethyldichlorosilane polymer