TETRAETHYLLEAD Chemical Properties

Melting point:

−136 °C(lit.)

Boiling point:

84-85 °C15 mm Hg(lit.)

Density 

1.653 g/mL at 25 °C(lit.)

refractive index 

n20/D 1.519(lit.)

Flash point:

84 °F

form 

liquid

Specific Gravity

1.653

Water Solubility 

insoluble H2O; soluble benzene, petroleum ether, gasoline [MER06]

Hydrolytic Sensitivity

4: no reaction with water under neutral conditions

Merck 

13,9277

Exposure limits

TLV-TWA 0.1 mg (Pb)/m³ (skin) (ACGIH)
PEL-TWA 0.075 mg (Pb)/m³ (skin) (OSHA).

Stability:

Stable. Highly flammable. Incompatible with strong oxidizing agents, concentrated acids. May dissolve some types of rubber. May be light sensitive. May detonate if confined at temperatures above 110 C.

CAS DataBase Reference

78-00-2(CAS DataBase Reference)

EPA Substance Registry System

Tetraethyllead (78-00-2)

Safety Information

Hazard Codes 

T+,N

Risk Statements 

61-26/27/28-33-50/53-62-38-10

Safety Statements 

53-45-60-61-36/37-26-28

RIDADR 

UN 1649 6.1/PG 1

OEB

D

OEL

TWA: 0.075 mg/m3 [skin]

WGK Germany 

3

RTECS 

TP4550000

TSCA 

Yes

HazardClass 

6.1(a)

PackingGroup 

I

Hazardous Substances Data

78-00-2(Hazardous Substances Data)

Toxicity

LD50 orally in rats: 12.3 mg/kg (Schroeder)

IDLA

40 mg Pb/m3

MSDS

• Language:English Provider:SigmaAldrich

TETRAETHYLLEAD Usage And Synthesis

Toxicity

Tetraethyl lead is a highly toxic compound manifesting both acute and chronic effects. These effects are insomnia, hypotension, hypothermia, tremor,weight loss, hallucination, nausea, convulsion and coma. LD50 oral (rats): 12 mg/kg.

Chemical Properties

colourless to yellow liquid

Chemical Properties

Tetraethyl lead is a colorless oily liquid. Sweet, slight musty odor. In commerce it is usually dyed red, orange or blue. Tetraethyl lead will decompose in bright sunlight yielding needlelike crystals of tri-, di-, and mono-ethyl lead compounds, which have a garlic odor.

Physical properties

Colorless liquid; burns with orange flame with green margin; refractive index 1.5198; density 1.653 g/mL at 20°C; insoluble in water; slightly soluble in ethanol; soluble in benzene, toluene, gasoline, and petroleum ether.

Uses

As a gasoline additive to prevent "knocking" in motors.Its use, however, is reduced drastically because of environmental pollution.

Uses

Anti-knock motor fuel additive

Uses

Tetraethyllead is used as an additive to gasolineto prevent knocking in motors. However,because of its high toxicity and the pollutionproblem, its use in gasoline has been drasticallycurtailed.

Production Methods

These compounds were, at one time, the major industrial use of lead and source of environmental pollution of inorganic lead combustion products. However, the addition of these compounds to gasoline in the major industrialized countries of the world has been discontinued because of the use of catalysts for the control of the amount of nitrogen oxides in automobile exhaust. Organolead additives are still being phased out in many underdeveloped countries, although the United Nations has called for a global phaseout of lead in gasoline.

Definition

A poisonous liquid that is insoluble in water but soluble in organic solvents. It is manufactured by the reaction of an alloy of sodium and lead with 1-chloroethane. The product is obtained by steam distillation. Lead tetraethyl is used as an additive in internal-combustion engine fuel to increase its octane number and thus prevent preignition (knocking).

Definition

ChEBI: An organolead compound consisting of four ethyl groups joined to a central lead atom.

Preparation

Lead tetraethyl is prepared by heating ethyl chloride in the presence of a catalyst in an autoclave at 40 to 60°C with an alloy of lead and sodium:
Pb + 4Na + 4C₂H₅Cl → Pb(C₂H₅)₄ + 4NaCl
Also, it can be prepared by the reaction of lead with ethylene and hydrogen in the presence of Ziegler catalyst, triethylaluminum:
Pb + 4C₂H₄ + 2H₂ → Pb(C₂H₅)₄

General Description

A colorless liquid with a characteristic odor. Flash point 200°F. Density 14 lb / gal. Insoluble in water. Toxic by inhalation and by skin absorption.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

TETRAETHYL LEAD decomposes under UV light. Reacts with fats; reacts violently with oxidizing agents, causing fire and explosion hazards. Attacks rubber [Handling Chemicals Safely 1980. p. 890].

Hazard

Toxic by ingestion, inhalation, and skin absorption. Central nervous system impairment. Questionable carcinogen.

Health Hazard

Extremely poisonous; may be fatal if inhaled, swallowed, or absorbed from the skin. Contact may cause burns to skin and eyes. Most symptoms of poisoning are due to the effects of tetraethyllead on the nervous system.

Health Hazard

Tetraethyllead is highly toxic by oral route.The LD50 values for rats, mice, andrabbits were all found to be <15 mg/kgwhen administered by the oral, intravenous,subcutaneous, intraperitoneal, and parenteralroutes. It may be absorbed through theskin causing lead poisoning. It is toxic tothe central nervous system. The toxicity,however, is low to moderate by dermal route.It is an acute as well as chronic toxicant.The toxic effects are insomnia, hypotension,tremor, hypothermia, pallor, weight loss,hallucination, nausea, convulsion, and coma.The toxicity of this compound by inhalationroute is also low to moderate. Because of itslow vapor pressure, 0.2 torr at 20°C (68°F),inhalation hazard is relatively low.
LD50 oral (rat): 12 mg/kg
Oral lethal dose (rabbit): 30 mg/kg
LC50 inhalation (rat): 850 mg/m³/1h.

Fire Hazard

May explode in fires. Decomposes slowly at room temperature and more rapidly at elevated temperatures.

Safety Profile

Human poison by an unspecified route. Experimental poison by ingestion, intraperitoneal, intravenous, subcutaneous, and parented routes. Moderately toxic by inhalation and skin contact. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic data. Mutation data reported. Lead compounds are particularly toxic to the central nervous system. It is a solvent for fatty materials and has some solvent action on rubber as well. The fact that it is a lipoid solvent makes it an industrial hazard because it can cause intoxication not only by inhalation but also by absorption through the skin. Decomposes when exposed to sunlight or allowed to evaporate; forms triethyl lead, which is also a poisonous compound, as one of its decomposition products. May cause elemental lead intoxication by coming in contact with the skin. A combustible liquid when exposed to heat, flame, or oxidizers. Can react vigorously with oxidzing materials. Exposure to air for several days may cause explosive decomposition. To fight fire, use dry chemical, CO2, mist, foam. When heated to decomposition it emits toxic fumes of Pb. See also LEAD COMPOUNDS.

Potential Exposure

Tetraethyl lead is used as a component of antiknock mixes for gas and as an intermediate in making fungicides; Tetraethyl lead (used as an antiknock compound in gasoline) can also contains impurities, such as ethylene dibromide and ethylene dichloride.

Carcinogenicity

A case-control study of former workers in a TEL-producing plant found a strong association between exposure to the TEL manufacturing process and rectal cancer (the odds ratio was 3.7 with 90% confidence limits of 1.3–10.2 for the analysis of ever/never exposed to TEL). An exposure–response relationship was noted with a fourfold elevation in the odds ratio at the high–very high cumulative exposure level. Similar results were obtained for cancers of the sigmoid colon. These results suggest to the authors that exposure to the TEL manufacturing process may have played a causal role in the colorectal cancer findings in this plant. However, IARC in 2006 has included organolead compounds (TEL and TML), with Lead and its Compounds in Group 3, not classifiable as to its carcinogenicity to humans.

Shipping

UN1649 Motor fuel antiknock mixtures, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

Its more volatile contaminants can be removed by exposure to a low pressure (by continuous pumping) for 1hour at 0o. Purify it by stirring with an equal volume of H2SO4 (d 1.40), keeping the temperature below 30o, repeating this process until the acid layer is colourless. It is then washed with dilute Na2CO3 and distilled water, dried with CaCl2 and fractionally distilled at low pressure under H2 or N2 [Calingaert Chem Rev 2 43 1926]. It prevents “knocking” in petrol combustion engines. [Milde & Beatty Adv Chem Res 23 306-318 1959, Beilstein 4 H 639.] VERY POISONOUS.

Incompatibilities

Vapors may form explosive mixture with air. A strong reducing agent. Violent reaction with strong oxidizers, sulfuryl chloride; halogens, oils and fats; rust, potassium permanganate. Decomposes slowly in light and at room temperature, and more rapidly at temperatures above 110C. Attacks rubber and some plastics and coatings.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥ 100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Controlled incineration with scrubbing for collection of lead oxides which may be recycled or land filled. It is also possible to recover alkyl lead compound from wastewaters as an alternative to disposal.

TETRAETHYLLEAD(78-00-2)Related Product Information

• Carbon tetrachloride
• Naphtha (petroleum), light alkylate
• Sodium nitrite
• Lead
• Tetramethyllead
• TETRAETHYLLEAD
• TETRA-N-BUTYLLEAD
• trimethyllead