Tricresyl phosphate

Tri-ortho-cresyl phosphate
Names
Preferred IUPAC name
Tris(2-methylphenyl) phosphate
Other names
tri-o-cresyl phosphate
TOCP
tritolyl phosphate, ortho-isomer
tri-o-tolyl ester of phosphoric acid
triorthocresyl phosphate (TOCP)
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.014.136
PubChem CID
RTECS number
  • o-: TD0350000
UNII
UN number 2574
InChI
  • InChI=1S/C21H21O4P/c1-16-10-4-7-13-19(16)23-26(22,24-20-14-8-5-11-17(20)2)25-21-15-9-6-12-18(21)3/h4-15H,1-3H3 Y
    Key: YSMRWXYRXBRSND-UHFFFAOYSA-N Y
  • o-: InChI=1/C21H21O4P/c1-16-10-4-7-13-19(16)23-26(22,24-20-14-8-5-11-17(20)2)25-21-15-9-6-12-18(21)3/h4-15H,1-3H3
    Key: YSMRWXYRXBRSND-UHFFFAOYAP
SMILES
  • o-: Cc3ccccc3OP(=O)(Oc1ccccc1C)Oc2ccccc2C
Properties
Chemical formula
C21H21O4P
Molar mass 368.37 g/mol
Appearance colourless liquid
Melting point −40 °C (−40 °F; 233 K)
Boiling point 255 °C (491 °F; 528 K) (10 mmHg)
Hazards
GHS labelling:
Pictograms
Signal word
Danger
Hazard statements
H370, H411
Precautionary statements
P260, P264, P270, P273, P307+P311, P321, P391, P405, P501
NFPA 704 (fire diamond)
1
1
0
Flash point > 225 °C (437 °F; 498 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Tricresyl phosphate (TCP), is a mixture of three isomeric organophosphate compounds most notably used as a flame retardant.[1] Other uses include as a plasticizer in manufacturing for lacquers and varnishes and vinyl plastics and as an antiwear additive in lubricants. Pure tricresyl phosphate is a colourless, viscous liquid, although commercial samples are typically yellow. It is virtually insoluble in water, but easily soluble in organic solvents like toluene, hexane, and diethyl ether among others. It was synthesized by Alexander Williamson in 1854 upon reacting phosphorus pentachloride with cresol (a mixture of para-, ortho-, and meta- isomers of methylphenol), though today's manufacturers can prepare TCP by mixing cresol with phosphorus oxychloride or phosphoric acid as well. TCP, especially the all-ortho isomer, is the causative agent in a number of acute poisonings. Its chronic toxicity is also of concern. The ortho-isomer is rarely used on its own outside of laboratory studies that require isomeric purity, due to its extremely toxic nature, and is generally excluded from commercial products where TCP is involved.

  1. ^ Weil, Edward D. (1978). "Phosphorus-Based Flame Retardants". Flame - Retardant Polymeric Materials. pp. 103–131. doi:10.1007/978-1-4684-6973-8_4. ISBN 978-1-4684-6975-2.