Description
p-tert-Butyltoluene is a colorless liquid withan aromatic gasoline-like odor. Molecular weight = 148.18;Boiling point = 193-194℃; Boiling point = 193℃;Freezing/Melting point = - 52℃; Vapor pressure =0.68 mmHg at 20℃; Flash point = 68℃. HazardIdentification (based on NFPA-704 M Rating System):Health 2, Flammability 2, Reactivity 0. Insoluble in water.
Chemical Properties
colourless liquid
Uses
4-tert-Butyltoluene is used as pharmaceutical intermediate, Solvent for resins, intermediate in organic synthesis. It is an intermediate for the production of the acaricide pyridaben.
Preparation
Synthesis of 4-tert-butyltoluene: Put toluene in the reaction kettle, add catalyst, then add tert-butane chloride, after the reaction, wash with water and layer, and the organic layer is distilled to obtain the product. Alkylation of isobutylene and toluene in the presence of sulfuric acid can also be used to produce 4-tert-butyltoluene.
General Description
Clear colorless liquid with an aromatic gasoline-like odor.
Air & Water Reactions
Flammable. Insoluble in water.
Reactivity Profile
4-tert-Butyltoluene may react with oxidizing materials.
Hazard
Toxic by inhalation, ingestion, and skin
absorption. Eye and upper respiratory tract irritant.
Health Hazard
p-tert-Butyl toluene is an irritant
of the mucous membranes, a central nervous
system depressant and may cause cardiovascular
and hematologic disturbances; chronic
exposure in animals causes lung, brain, liver,
and kidney damage.
Fire Hazard
4-tert-Butyltoluene is combustible.
Safety Profile
Moderately toxic by
inhalation and ingestion. A skin and human
eye irritant. Human systemic effects by
inhalation: nausea or vomiting, conjunctiva
irritation, unspecified effects on the sense of
taste. Inhalation of vapors causes irritation
of lungs and depression of central nervous
system. Prolonged exposure may result in
damage to liver and kidneys. Flammable
when exposed to heat or flame.
Incompatible with oxidizing materials.
When heated to decomposition it emits
acrid smoke and fumes.
Potential Exposure
Human Data;Primary Irritant. This material is used as a solvent for resinsand as an intermediate in organic synthesis.
First aid
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seekmedical attention immediately. If this chemical contactsthe skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove fromexposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing hasstopped and CPR if heart action has stopped. Transferpromptly to a medical facility. When this chemical hasbeen swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.
Carcinogenicity
p-tert-Butyl toluene was not mutagenic in
a number of bacterial strains in the Ames assay
with or without metabolic activation.
storage
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, wellventilated area. Sources of ignition, such as smoking andopen flames, are prohibited where this chemical is used,handled, or stored in a manner that could create a potentialfire or explosion hazard.
Shipping
Butyltoluenes require a “POISONOUS/TOXICMATERIALS” label. They fall in Hazard Class 6.1 andPacking Group III.[19, 20]
Purification Methods
A sample containing 5% of the meta-isomer is purified by selective mercuration. Fractional distillation of the solid arylmercuric acetate, after removal from the residual hydrocarbon, gives pure p-tert-butyltoluene [Stock & Brown J Am Chem Soc 81 5615 1959]. [Beilstein 5 H 439, 5 III 1003, 5 IV 1079.]
Incompatibilities
Forms explosive mixture with air. Reactswith strong oxidizers. May accumulate static electricalcharges and may cause ignition of its vapors
