4-tert-Butylcatechol Property

Melting point:

52-55 °C(lit.)

Boiling point:

285 °C(lit.)

Density 

1.049

vapor pressure 

<1 hPa (25 °C)

refractive index 

n20/D 1.508

Flash point:

>230 °F

storage temp. 

Store below +30°C.

solubility 

methanol: soluble1g/10 mL, clear, colorless to slightly yellow

pka

9.92±0.10(Predicted)

form 

powder to lump

color 

White to Light yellow to Light red

Odor

at 10.00?%?in?dipropylene glycol. phenolic

Water Solubility 

0.2 g/100 mL (25 ºC)

Sensitive 

Hygroscopic

BRN 

2043335

Exposure limits

ACGIH: TWA 5 ppm (Skin)
NIOSH: TWA 5 ppm(20 mg/m3)

InChIKey

XESZUVZBAMCAEJ-UHFFFAOYSA-N

LogP

1.98 at 25℃

CAS DataBase Reference

98-29-3(CAS DataBase Reference)

NIST Chemistry Reference

1,2-Benzenediol, 4-(1,1-dimethylethyl)-(98-29-3)

EPA Substance Registry System

p-tert-Butylcatechol (98-29-3)

Safety

Hazard Codes 

C,N,T

Risk Statements 

22-34-43-21-51/53-21/22-39/23/24/25-20/21/22-10-50/53

Safety Statements 

26-36/37/39-45-61-24-60

RIDADR 

UN 2923 8/PG 3

WGK Germany 

2

RTECS 

UX1400000

Autoignition Temperature

160 °C

TSCA 

Yes

HazardClass 

8

PackingGroup 

III

HS Code 

29072900

Toxicity

LD50 orally in Rabbit: 815 mg/kg LD50 dermal Rat 1331 mg/kg

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H314Causes severe skin burns and eye damage

H317May cause an allergic skin reaction

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P273Avoid release to the environment.

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

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

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

4-tert-Butylcatechol Chemical Properties,Usage,Production

Description

Para-tertiary butyl catechol is specially prepared by reacting the impure catechol fraction with tertiary butyl alcohol. Used for its various properties (inhibition of polymerization and as an antioxidizing agent) in the manufacture of rubber, plastics and paints, in the preparation of petrolatum products, and as an antioxidant in oils, it may induce vitiligo.

Chemical Properties

white to cream flakes

Uses

Polymerization inhibitor for styrene-butadiene and other olefins.
Inhibitor-remover packings and ready-to-use, disposable prepacked columns offer a quick and convenient means of removing small amounts of inhibitors which are added to reagents or solvents that would otherwise be unstable (e.g., they may polymerize, oxidize or darken) on storage.
The inhibitor removers are useful in applications which require that the stabilizer or inhibitor [i.e., hydroquinone (HQ), hydroquinone monomethyl ether (MEHQ, 4-methoxyphenol) or 4-tert-butylcatechol (TBC)] be removed prior to use.

Uses

4-tert-butylcatechol (PTBC) is used as an antioxidant in fats, oils, and mineral oils, and as a stabilizer in polyester resins and polystyrene resins. A concentration of PTBC (up to 0.005%) can be found in paints, glues, thermal paper, lubricating oil, and mineral oil products.
4-tert-Butylcatechol is widely utilized as an inhibitor in polymerization of butadiene, styrene, vinyl acetate and other reactive monomers. It plays an important role in the synthesis of tungsten oxide nanoparticles by nonaqueous sol-gel process. It acts as a stabilizer in the manufacturing of polyurethane foam. It is employed as an antioxidant for synthetic rubber, polymers and oil derivatives. It is also utilized as a purification agent for aminoformate catalysts.

General Description

4-tert-Butylcatechol,in the presence of O₂ catalyzed by tyrosinase, yields 4-tert-butyl-o-benzoquinone. Electrochemical oxidation of 4-tert-Butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic voltammetry and controlled-potential coulometry. It undergoes electrochemical trimerization via anodic oxidation and mechanism of trimerization has been studied using cyclic voltammetry and controlled-potential coulometry.

Hazard

Toxic by ingestion and skin absorption.

Flammability and Explosibility

Not classified

Contact allergens

p-tert-Butyl catechol is specially prepared by reacting the impure catechol fraction with tertiary butyl alcohol. It is used for its various properties (inhibitor of polymerization and antioxidizing agent) in the manufacture of rubber, plastics, and paints, in the preparation of petrolatum products, and as an antioxidant in oils. It may induce vitiligo.

Safety Profile

A poison by intravenous route. Moderately toxic by ingestion and skin absorption. A severe skin and eye irritant. Mutation data reported. Combustible when exposed to heat or flame. To fight fire, use Con, dry chemical, fog, mist. When heated to decomposition it emits acrid and irritating fumes

Purification Methods

Distil it in a vacuum, then recrystallise it from pentane or pet ether (or *C6H6). [Beilstein