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Tri-o-cresyl Phosphate

Tri-o-cresyl Phosphate Structure
CAS No.
78-30-8
Chemical Name:
Tri-o-cresyl Phosphate
Synonyms
TOCP;Tofk;TOTP;NCLC61041;Plastic X;phosflex179c;tri-o-cresyl;Phosflex 179C;Tri-2-cresyl p;triorthocresyl
CBNumber:
CB3466623
Molecular Formula:
C21H21O4P
Molecular Weight:
368.36
MOL File:
78-30-8.mol
Modify Date:
2023/7/4 17:14:15

Tri-o-cresyl Phosphate Properties

Melting point -25 °C
Boiling point 410 °C
Density 1.2
vapor pressure 0.195 at 50 °C (Carré and Bertrans, 1998)
refractive index 1.558-1.561
Flash point 225 °C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility sparingly soluble in water; soluble in acetic acid; freely soluble in alcohol, benzene, ether; very soluble in carbon tetrachloride, toluene.
maximum allowable concentration: 0.1 mg/m3 (TLV-TWA) (ACGIH 1986)
form Viscous Liquid
color Clear colorless to yellow
Merck 14,9764
Exposure limits TLV-TWA skin 0.1 mg/m3 (ACGIH and OSHA); IDLH 40 mg/m3 (NIOSH).
CAS DataBase Reference 78-30-8(CAS DataBase Reference)
EPA Substance Registry System Tri-o-cresyl phosphate (78-30-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08,GHS09
Signal word  Danger
Hazard statements  H370-H411
Precautionary statements  P260-P264-P270-P307+P311-P321-P405-P501
Hazard Codes  N-T,N,T
Risk Statements  51/53-39/23/24/25
Safety Statements  61-45-28A-20/21-28
RIDADR  3082
OEB D
OEL TWA: 0.1 mg/m3 [skin]
RTECS  TD0350000
HazardClass  6.1(a)
PackingGroup  II
HS Code  29199000
Toxicity Acute oral LD50 for rats 160 mg/kg (quoted, RTECS, 1985).
IDLA 40 mg/m3
NFPA 704
1
2 0

Tri-o-cresyl Phosphate price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) P1331 Tri-o-cresyl Phosphate min. 97.0 % 78-30-8 5G ₹8800 2022-05-26 Buy
TCI Chemicals (India) P1331 Tri-o-cresyl Phosphate min. 97.0 % 78-30-8 25G ₹25600 2022-05-26 Buy
Product number Packaging Price Buy
P1331 5G ₹8800 Buy
P1331 25G ₹25600 Buy

Tri-o-cresyl Phosphate Chemical Properties,Uses,Production

Chemical Properties

Tricresyl phosphates are available as the o-isomer (TOCP), the m-isomer (TMCP), and p-isomer (TPCP). The ortho-isomer is the most toxic of the three; the meta-and para-isomers are relatively inactive. The commercial product may contain the ortho-isomer as a contaminant unless special precautions are taken during manufacture. Pure tri-para-cresyl phosphate is a solid, and ortho-and meta-are liquids (see below). The tri-o-cresyl phosphate will be discussed here as the specific example of these compounds because it is the most toxic of the tricresyl phosphates and specifically regulated by OSHA. TOCP is a colorless to pale yellow, odorless liquid or solid (below 52/F/11℃).

Physical properties

Tri-o-cresyl phosphate is a colorless to pale yellow, odorless to faint aromatic-like liquid, and it is a solid below the 25.6 °C melting point. It is sparingly soluble in water, but is slightly soluble in ethanol and very soluble in ethyl ether (Budavari, 1996). The vapor pressure of TOCP is 0.00002mm Hg at room temperature, but is 10mm Hg at 265 °C (Bisesi, 1994). It decomposes slightly upon boiling (bp 410 °C) (Budavari, 1996).

Uses

Tri-o-cresyl phosphate is used widely as a gasoline additive, plasticizer, fire retardant, solvent, extreme pressure additive, intermediate in pharmaceutical manufacturing, water-proofing agent, heat exchange medium, and as a lead scavenger in gasoline.

Production Methods

Prepared from cresol and phosphorus oxychloride, phosphoric acid, or phosphorus pentachloride. The grades of cresol commonly used are the isomeric (o-, m-, /p-), and meta-para mixtures from coal tar and cresylic acid from petroleum. Purification of the product is based on the intended use; the commercial product is generally obtained as a mixture. A 'refined grade' of tricresyl phosphate is prepared by vacuum distillation, or alternatively by washing with 2% NaOH and water (Lowenheim and Moran 1975).

Hazard

Toxic by ingestion and skin absorption. The oisomer is highly toxic. TLV: 0.1 mg/m3 (skin); not classifiable as a Human Carcinogen.

Health Hazard

TOCP is a highly poisonous compound. Its toxicity is greater than that of the meta- or para-isomer. The toxic routes are inhalation, ingestion, and absorption through the skin; and the symptoms varied with the species and the route of admission.
Ingestion of 40–60 mL of the liquid can be fatal to humans. An oral dose of 6–7 mg/kg has produced serious paralysis in humans (Patty 1949). The toxic symptoms from oral intake can be gastrointestinal pain, diarrhea, weakness, muscle pain, kidney damage, and paralysis. The target organs are the gastrointestinal tract, kidney, central nervous system, and neuromuscular system.
LD50 value, oral (rabbits): 100 mg/kg
Somkuti et al. (1987) reported testicular toxicity of TOCP in adult leghorn roosters. Birds dosed with 100 mg/kg/day exhibited limb paralysis in 7–10 days. Such symptoms are characteristics of delayed neurotoxicity caused by organophosphorus compounds. Analysis at the termination of 18 days indicated a significant inhibition of neurotoxic esterase activity in both brain and testes, and a decrease in sperm motility and brain acetylcholinesterase activity.
TOCP caused adverse reproductive effects in mice, such as increased maternal mortality and a decreased number of viable litters. An LD50 value of 515 mg/kg/day is reported
(Environmental Health Research and Testing 1987)..

Fire Hazard

Noncumbustible solid; vapor pressure 0.02 torr at 150°C (302°F); fire retardant.

Industrial uses

1. As additive to extreme pressure lubricants.
2. As a non-flammable fluid in hydraulic systems.
3. As plasticizer in lacquers and varnishes.
4. As plasticizer in vinyl plastics manufacture.
5. As flame retardant.
6. As lead scavenger in gasoline.
7. As solvent for nitrocellulose, in cellulosic molding compositions.

Safety Profile

Poison by subcutaneous, intramuscular, intravenous, and intraperitoneal routes. Moderately toxic by ingestion. Most of the cases of tri-o-cresyl phosphate poisoning have followed its ingestion. In 1930, some 15,000 persons were affected in the United States, and of these, 10 died. The responsible material was found to be an alcoholic drink known as Jamaica ginger, or "jake." This beverage had been adulterated with about 2% of tri-o-cresyl phosphate. The affected persons developed a polyneuritis, which progressed, in many cases, with degeneration of the peripheral motor nerves, the anterior horn cells, and the pyramidal tracts. Sensory changes were absent. Since 1930 there have been several other outbreaks of poisoning following ingestion of the material. Tri-ocresyl phosphate is more toxic than the mform, and much more so than tri-p-cresyl phosphate or triphenyl phosphate. Experimental reproductive effects. flame. Can react with oxidizing materials. To fight fire, use CO2, dry chemical. When heated to decomposition it emits highly toxic fumes of POx. See also PHOSPHATES. Combustible when exposed to heat or

Potential Exposure

Tricresyl phosphate is used as an additive in hydraulic fluids; as a plasticizer; pigment dispersant; flame retardant; as a plasticizer for chlorinated rubber; vinyl plastics; polystyrene, polyacrylic, and polymethacrylic esters; as an adjuvant in milling of pigment pastes; as a solvent and as a binder in nitrocellulose and various natural resins, and as an additive to synthetic lubricants and gasoline. It is also used in the recovery of phenol in coke-oven wastewaters.

Environmental Fate

Biological. A commercial mixture containing tricresyl phosphates was completely degraded by indigenous microbes in Mississippi River water to carbon dioxide. After 4 wk, 82.1% of the theoretical carbon dioxide had evolved (Saeger et al., 1979).
Chemical/Physical. Tri-o-cresyl phosphate hydrolyzed rapidly in Lake Ontario water, presumably to di-o-cresyl phosphate (Howard and Doe, 1979). When an aqueous solution containing a mixture of isomers (0.1 mg/L) and chlorine (3 to 1,000 mg/L) was stirred in the dark at 20 °C for 24 h, the benzene ring was substituted with one to three chlorine atoms (Ishikawa and Baba, 1988).
Decomposes at temperatures greater than 424 °C (Dobry and Keller, 1957).

Shipping

UN2574 Tricresyl phosphate with >3% ortho (o-) isomer, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Contact with magnesium may cause explosion. Organophosphates, such as tricresyl phosphate, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrideds and active metals. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Waste Disposal

TOCP is dissolved in a combustible solvent and burned in a chemical incinerator equipped with an afterburner and scrubber.

Tri-o-cresyl Phosphate Preparation Products And Raw materials

Global( 95)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Allchem Lifescience Pvt. Ltd +919867655500 Gujarat, India 971 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +8613288715578 China 12452 58 Inquiry
Jinan Carbotang Biotech Co.,Ltd. +8615866703830 China 7513 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +86-19930503282 China 8822 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29825 58 Inquiry
Zhengzhou Alfa Chemical Co.,Ltd +8618530059196 China 13193 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
O-TOLYL PHOSPHATE PHOSPHORIC ACID TRI-O-CRESYL ESTER PHOSPHORIC ACID TRI-O-TOLYL ESTER TRI-O-CRESYL PHOSPHATE TRI-O-TOLYL PHOSPHATE NCLC61041 o-Cresyl phosphate o-cresylphosphate o-Trikesylphosphate o-trikresylphosphate o-Trioyl phosphate Phosflex 179C phosflex179c phosphatedetri-o-cresyle Phosphoric acid, tri-2-methylphenyl ester Phosphoric acid, tri-o-cresyl ether Phosphoric acid, tris(2-methylphenyl) ester phosphoricacid,tri(2-tolyl)ester Phosphoricacid,tris(2-methylphenyl)ester TriTri-o-tolyl phosphate tricresyl phosphate tritolyl phosphate o-o-o, o-o-m, o-o-p, o-m-m, o-m-p, o-p-p Phosphoric acid tris(o-tolyl) ester Tri-o-tolyl phosphate,96% Tri-o-tolyl phosphate,98% Isopropylated Triaryl Phoshate Tri-o-tolyl phosphate, 96% 100GR Phosphoric Acid Tri-o-tolyl Ester Phosphoric Acid Tri-o-cresyl Ester Tri-o-tolyl Phosphate Tri-2-cresyl p tri-2-cresyl phosphate O-TRICRESYLPHOSPHATE ORTHO-TRICRESYLPHOSPHATE TRI-ORTHO-CRESOLPHOSPHATE TRIS(2-TOLYL)-PHOSPHATE ORTHO-CRESYLPHOSPHATE TRI-ORTHO-TOLYLPHOSPHATE phosphoricacidtri(2-methylphenyl)ester Plastic X TOCP Tofk TOTP Tri-2-methylphenyl phosphate tri2-methylphenylphosphate Tri-2-tolyl phosphate tri-2-tolylphosphate tricresylphosphate(non-specificname) tri-o-cresyl Tri-o-kcresylphosphate triorthocresyl Triorthocresyl phosphate triorthocresylphosphate tri-ortho-cresylphosphate Tri-O-tolyl ester phosphoric acid Tris(2-methylphenyl) phosphate Tris(o-cresyl)-phosphate Tris(o-methylphenyl)phosphate Tris(o-tolyl) phosphate tris(o-tolyl)phosphate tris(o-tolyl)-phosphate