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Tri-o-tolylphosphat

Tri-o-cresyl Phosphate Struktur
78-30-8
CAS-Nr.
78-30-8
Bezeichnung:
Tri-o-tolylphosphat
Englisch Name:
Tri-o-cresyl Phosphate
Synonyma:
TOCP;Tofk;TOTP;NCLC61041;Plastic X;phosflex179c;tri-o-cresyl;Phosflex 179C;Tri-2-cresyl p;triorthocresyl
CBNumber:
CB3466623
Summenformel:
C21H21O4P
Molgewicht:
368.36
MOL-Datei:
78-30-8.mol

Tri-o-tolylphosphat Eigenschaften

Schmelzpunkt:
-25 °C
Siedepunkt:
410 °C
Dichte
1.2
Dampfdruck
0.195 at 50 °C (Carré and Bertrans, 1998)
Brechungsindex
1.558-1.561
Flammpunkt:
225 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
L?slichkeit
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)
Aggregatzustand
Viscous Liquid
Farbe
Clear colorless to yellow
Merck 
14,9764
Expositionsgrenzwerte
TLV-TWA skin 0.1 mg/m3 (ACGIH and OSHA); IDLH 40 mg/m3 (NIOSH).
CAS Datenbank
78-30-8(CAS DataBase Reference)
EPA chemische Informationen
Tri-o-cresyl phosphate (78-30-8)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher N-T,N,T
R-S?tze: 51/53-39/23/24/25
S-S?tze: 61-45-28A-20/21-28
OEB D
OEL TWA: 0.1 mg/m3 [skin]
RIDADR  3082
RTECS-Nr. TD0350000
HazardClass  6.1(a)
PackingGroup  II
HS Code  29199000
Giftige Stoffe Daten 78-30-8(Hazardous Substances Data)
Toxizit?t Acute oral LD50 for rats 160 mg/kg (quoted, RTECS, 1985).
IDLA 40 mg/m3
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H370 Sch?digt die Organe. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P307+P311, P321,P405, P501
H411 Giftig für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gew?ssergef?hrdend Kategorie 2
Sicherheit
P260 Dampf/Aerosol/Nebel nicht einatmen.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P307+P311 BEI Exposition: GIFTINFORMATIONSZENTRUM oder Arzt anrufen.
P321 Besondere Behandlung
P405 Unter Verschluss aufbewahren.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Tri-o-tolylphosphat Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

FARBLOSE ODER SCHWACH GELBE FLüSSIGKEIT

CHEMISCHE GEFAHREN

Zersetzung beim Erhitzen unter Bildung giftiger Rauche mit Phosphoroxiden. Reagiert mit Oxidationsmitteln.

ARBEITSPLATZGRENZWERTE

TLV: 0.1 mg/m?(als TWA); Hautresorption; BEI vorhanden; Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); (ACGIH 2006).
MAK nicht festgelegt (DFG 2006).

AUFNAHMEWEGE

Aufnahme in den K?rper durch Inhalation und über die Haut sowie durch Verschlucken.

INHALATIONSGEFAHREN

Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitssch?dliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
M?glich sind Auswirkungen auf das Zentralnervensystem und das periph?re Nervensystem. Exposition oberhalb des Arbeitsplatzgrenzwertes kann zu Degeneration des Nervensystems führen. Die Auswirkungen treten u.U. verz?gert ein. ?rztliche Beobachtung notwendig.

WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION

M?glich sind Auswirkungen auf das Nervensystem.

LECKAGE

Chemikalienschutzanzug mit umgebungsluftunabh?ngigem Atemschutzger?t. Ausgelaufene Flüssigkeit in abdichtbaren Beh?ltern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Umwelt gelangen lassen.

R-S?tze Betriebsanweisung:

R51/53:Giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.

S-S?tze Betriebsanweisung:

S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S20/21:Bei der Arbeit nicht essen, trinken,rauchen.
S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).

Chemische Eigenschaften

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℃).

Physikalische Eigenschaften

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).

Verwenden

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.

Vorbereitung Methode

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)..

Brandgefahr

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

Industrielle Verwendung

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.

Sicherheitsprofil

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

m?gliche Exposition

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).

Versand/Shipping

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

Inkompatibilit?ten

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-tolylphosphat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Tri-o-tolylphosphat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 100)Lieferanten
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Hebei Mojin Biotechnology Co., Ltd
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Jinan Carbotang Biotech Co.,Ltd.
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78-30-8(Tri-o-tolylphosphat)Verwandte Suche:


  • 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
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