Methyltriphenylphosphonium bromide CAS# 1779-49-3
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Chemical Name:Methyltriphenylphosphonium bromide
CAS No:1779-49-3
Molecular Formula:C19H18BrP
Molecular weight:357.22
Sample: Available
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Products Description of Methyltriphenylphosphonium bromide CAS# 1779-49-3
Methyltriphenylphosphonium bromide is a solid quaternary phosphonium salt flame retardant. At present, halogen-containing flame retardants are widely used organic flame retardants with excellent flame retardant properties. However, when a fire occurs, halogen-containing flame retardants will release a large amount of smoke and toxic hydrogen halide gas, causing secondary hazards. With the promulgation of the EU RoHs and WEEE directives, the application of organic halogen-containing flame retardants in the fields of electronic and electrical equipment has been subject to many restrictions. Therefore, the development of high-efficiency halogen-free flame retardants has become a very important topic.
Methyltriphenylphosphonium bromide Chemical Properties
Melting point | 230-234 °C (lit.) |
vapor pressure | 0.0000002 hPa |
Fp | >240°C |
storage temp. | Inert atmosphere,Room Temperature |
solubility | H2O: 0.1 g/mL, clear |
form | Powder |
color | White |
PH | 6.0-6.5 (400g/l, H2O, 20℃) |
Water Solubility | 400 g/L (25 ºC) |
Sensitive | Hygroscopic |
BRN | 3599467 |
InChIKey | LSEFCHWGJNHZNT-UHFFFAOYSA-M |
LogP | -1.18 |
CAS DataBase Reference | 1779-49-3(CAS DataBase Reference) |
NIST Chemistry Reference | Methyltriphenylphosphonium bromide(1779-49-3) |
EPA Substance Registry System | Phosphonium, methyltriphenyl-, bromide (1779-49-3) |
Safety Information
Hazard Codes | Xn,Xi |
Risk Statements | 20/21/22-36/37/38 |
Safety Statements | 36/37-36-26 |
RIDADR | UN 1390 4.3/PG 2 |
WGK Germany | 3 |
Autoignition Temperature | 410 °C |
TSCA | T |
HazardClass | 6.1 |
PackingGroup | III |
HS Code | 29310095 |
Toxicity | LD50 orally in Rabbit: 118 mg/kg |
Product Application of Methyltriphenylphosphonium bromide CAS# 1779-49-3
Methyltriphenylphosphonium bromide can be used as a Wittig reagent for the preparation of olefins and for increasing the carbon number of unsaturated carbon chains. It is a ylide precursor of the Wittig reaction and is widely used in the synthesis of unsaturated bonds in liquid crystal materials. It is also widely used in organic synthesis. It is a good cationic phase transition catalyst.
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