4-tert-Butylphenol Property

Melting point:

96-101 °C (lit.)

Boiling point:

236-238 °C (lit.)

Density 

0.908 g/mL at 25 °C (lit.)

vapor pressure 

1 mm Hg ( 70 °C)

refractive index 

1.4787

FEMA 

3918 | P-TERT-BUTYLPHENOL

Flash point:

113 °C

storage temp. 

Store below +30°C.

solubility 

ethanol: soluble50mg/mL, clear, colorless

form 

Flakes or Pastilles

pka

10.23(at 25℃)

color 

White to light beige

Specific Gravity

0.908

Odor

at 1.00 % in propylene glycol. oakmoss leather

PH

7 (10g/l, H2O, 20℃)

explosive limit

0.8-5.3%(V)

Odor Type

leathery

Water Solubility 

8.7 g/L (20 ºC)

JECFA Number

733

Merck 

14,1585

BRN 

1817334

Stability:

Stable. Incompatible with copper, steel, bases, acid chlorides, acid anhydrides, oxidizing agents.

InChIKey

QHPQWRBYOIRBIT-UHFFFAOYSA-N

LogP

3 at 23℃

CAS DataBase Reference

98-54-4(CAS DataBase Reference)

NIST Chemistry Reference

Phenol, p-tert-butyl-(98-54-4)

EPA Substance Registry System

p-tert-Butylphenol (98-54-4)

Safety

Hazard Codes 

Xi,N

Risk Statements 

37/38-41-51/53-62-38-37-34

Safety Statements 

26-39-61-36/37/39-45

RIDADR 

UN 3077 9/PG 3

WGK Germany 

2

RTECS 

SJ8925000

TSCA 

Yes

HazardClass 

8

PackingGroup 

III

HS Code 

29071900

Hazardous Substances Data

98-54-4(Hazardous Substances Data)

Toxicity

LD50 orally in rats: 3.25 ml/kg (Smyth)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H315Causes skin irritation

H318Causes serious eye damage

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

4-tert-Butylphenol Chemical Properties,Usage,Production

Description

Para-tertiary-butylphenol formaldehyde resin (PTBPF- R) is a polycondensate of para-tertiary-butylphenol and formaldehyde. Major occupational sources are neoprene glues and adhesives in industry, in the shoemaking and leather industry or in car production. It is also used as a box preservative in box and furniture manufacture, and in the production of casting moulds, car-brake linings, insulated electrical cables, adhesives, printing inks and paper laminates. Para-tertiary-butyl-phenol is the sensitizer.

Chemical Properties

4-tert-Butylphenol is a white to pale yellow crystalline solid at room temperature and is sold in solid form as flakes or briquettes. 4-tert-butylphenol is employed in coating products, polymers, adhesives, sealants and for the synthesis of other substances.
The major use is as a monomer in chemical synthesis, e.g. for the production of polycarbonate, phenolic resins, epoxy resins. PtBP is used as a chain terminator in the synthesis of polycarbonate polymers. The main uses of polycarbonate are in compact discs, DVD and CD Rom manufacture.

Occurrence

Reported found in origanum (Coridothymus cap. (L.) Richb.)

Uses

4-tert-butylphenol on condensation with formaldehyde gives calix[5]arene which is used in enzyme mimetics.

Uses

4-tert-Butylphenol is a phenol derivative. Its contact with skin may lead to leukoderma. It is widely used in the polymer industry. Reaction of 4-tert-Butylphenol with mushroom tyrosinase has been reported to afford 4-t-butyl-o-benzoquinone and kinetics of this enzymatic reaction has been investigated.

Uses

Polycarbonate Chain Terminator, Glycidyl Ethers; Phosphate Esters, Fragrances, Oil Field Chemicals-Demulsifiers; Plasticizer for cellulose acetate; intermediate for antioxidants, special starches, oil-soluble phenolic resins; pour-point depressors and emulsion breakers for petroleum oils and some plastics; synthetic lubricants; insecticides; industrial odorants; motor-oil additives.

Preparation

Prepared by heating phenol with isobutanol in the presence of zinc chloride; also from phenol, tert- butyl chloride and excess alkali in alcohol

Application

4-tert-Butylphenol may be employed as carbon and energy supplement in the culture medium of Sphingobium fuliginis strains.
4-tert-Butylphenol is suitable reagent used in kinetic study of hydroxylation of 4-tert-butylphenol by mushroom tyrosinase. It may be used in the synthesis of calix[7]arene.

Definition

ChEBI: 4-tert-butylphenol is a member of the class of phenols that is phenol substituted with a tert-butyl group at position 4. It has a role as an allergen.

Synthesis Reference(s)

The Journal of Organic Chemistry, 22, p. 988, 1957 DOI: 10.1021/jo01359a609

General Description

Crystals or practically white flakes. Has a disinfectant-like odor. May float or sink in water. Insoluble in water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Phenols, such as 4-tert-Butylphenol, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

Hazard

Irritant to eyes and skin.

Fire Hazard

Combustible.

Contact allergens

Para-tert-butylphenol is used with formaldehyde to produce the polycondensate p-tert-butylphenol-formaldehyde resins (PTBPFR). Major occupational sources are neoprene glues and adhesives in industry, in the shoemaking and leather industries or in car production. It is also used as a box preservative in box and furniture manufacture and in the production of casting molds, car brake linings, insulated electrical cables, adhesives, printing inks, and paper laminates. Para-tertbutylphenol seems to be the sensitizer

Safety Profile

Poison by intraperitoneal route. Moderately toxic by skin contact and ingestion. A skin and severe eye irritant. Questionable carcinogen with experimental neoplastigenic data. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid and irritating fumes. See also PHENOL and other butyl phenols.

Potential Exposure

Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a germicidal agent in detergent disinfectants; as a pour point depressant, in motor-oil additives; de-emulsifier for oil; soap-antioxidant, plasticizer, fumigant, and insecticide

Shipping

UN2430 Alkylphenols, solid, n.o.s. (including C2-C12 homologues), Hazard class: 8; Labels: 8— Corrosive material

Purification Methods

Crystallise the phenol to constant melting point from pet ether (b 60-80o). It sublimes in vacuo. Also purify it via the benzoate, as for phenol. The salicylate ester [87-18-30] has m 63-64o (from aqueous EtOH, or EtOH). [Beilstein 6 IV 3296.]

Incompatibilities

Vapors may form explosive mixture with air. These phenol/cresol materials can react with oxidizers; reaction may be violent. Incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may cause the gas to ignite and explode. Heat is also generated by the acid-base reaction with bases; such heating may initiate polymerization of the organic compound. React with boranes, alkalies, aliphatic amines, amides, nitric acid, sulfuric acid. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). These reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid and can explode when heated. Many phenols form metal salts that may be detonated by mild shock