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Diisopropyl phosphite

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Diisopropyl phosphite Basic information

Product Name:
Diisopropyl phosphite
Synonyms:
  • Diisopropyl hydrogen phosphonate
  • Diisopropylphosphine oxide
  • Isopropyl phosphonate
  • Isopropyl phosphonate ((C3H7O)2HPO)
  • isopropylphosphonate
  • O,O-Diisopropyl phosphonate
  • o,o-diisopropylphosphite
  • o,o-diisopropylphosphonate
CAS:
1809-20-7
MF:
C6H15O3P
MW:
166.16
EINECS:
217-317-7
Product Categories:
  • organophosphorus compound
  • Miscellaneous Reagents
  • bc0001
Mol File:
1809-20-7.mol
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Diisopropyl phosphite Chemical Properties

Boiling point:
71 °C (8 mmHg)
Density 
0.997
refractive index 
1.4065-1.4085
Flash point:
69°C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Sparingly), Methanol (Sparingly)
form 
Liquid
Specific Gravity
1
color 
Clear colorless
Water Solubility 
soluble
Sensitive 
Moisture Sensitive
CAS DataBase Reference
1809-20-7(CAS DataBase Reference)
NIST Chemistry Reference
Phosphonic acid, di-isopropyl ester(1809-20-7)
EPA Substance Registry System
Phosphonic acid, bis(1-methylethyl) ester (1809-20-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26
RIDADR 
3265
RTECS 
SZ7660000
TSCA 
Yes
HS Code 
29209085
Toxicity
guinea pig,LC50,inhalation,9010mg/m3 (9010mg/m3),LUNGS, THORAX, OR RESPIRATION: OTHER CHANGESGASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDSBEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD,Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 29(11), Pg. 51, 1985.

MSDS

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Diisopropyl phosphite Usage And Synthesis

Chemical Properties

clear colourless liquid, corrosive, soluble in organic solvents such as ethanol.

Uses

Diisopropyl phosphite is used as antiwear lubricant additive together with triphenyl thiophosphate on T8 steel/Al2O3 ceramics.

Preparation

Diisopropyl phosphite is prepared by directly reacting isopropanol with phosphorus trichloride.
3(CH3)2CHOH+PCl3→[(CH3)2CHO]2POH+2HCl↑+(CH3)2CHCl
At a ratio of 3:1 (mol), continuously feed 215kg/h of isopropanol and 150kg/h of phosphorus trichloride. When mixed, this results in a violent reaction that generates hydrogen chloride gas. This gas is quickly removed from the mixing pot using vacuum mercury. The crude ester produced is then heated in a falling film type spinner deacidification device and further deacidified. The resulting product is then cooled to below 40°C and obtained with a content of 92%-95% and a yield of 95%~98%.

Synthesis Reference(s)

Tetrahedron Letters, 29, p. 3327, 1988 DOI: 10.1016/0040-4039(88)85153-0

Diisopropyl phosphite Preparation Products And Raw materials

Raw materials

Preparation Products

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