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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