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3,5-Di-tert-butylcatechol

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3,5-Di-tert-butylcatechol Basic information

Product Name:
3,5-Di-tert-butylcatechol
Synonyms:
  • 1,2-Dihydroxy-3,5-di(tert-butyl)benzene, 3,5-Di(tert-butyl)catechol
  • 3,5-Di-tert-butylcatechol, 99% 25GR
  • 3,5-Di-tert-butylcatechol, 99% 5GR
  • 3,5-bis(1,1-dimethylethy
  • 1,5-Bis(tert-butyl)-2,3-dihydroxybenzene, 3,5-Bis(tert-butyl)catechol
  • 3,5-Bis(tert-butyl)benzene-1,2-diol
  • 3,5-Di-tert-butylcatechol
  • 1,2-Benzenediol, 3,5-di(1,1-dimethylethyl)-
CAS:
1020-31-1
MF:
C14H22O2
MW:
222.32
EINECS:
213-816-9
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Organic Building Blocks
  • Oxygen Compounds
  • Aromatic Phenols
  • Aromatic Ethers
  • Naphthyridine,Quinoline
  • Polyols
Mol File:
1020-31-1.mol
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3,5-Di-tert-butylcatechol Chemical Properties

Melting point:
95-100 °C(lit.)
Boiling point:
145 °C / 5mmHg
Density 
1.0200 (rough estimate)
refractive index 
1.4576 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
form 
Solid
pka
10.04±0.15(Predicted)
color 
White to pale brown
Water Solubility 
Insoluble in water.
BRN 
1370212
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference
1020-31-1(CAS DataBase Reference)
NIST Chemistry Reference
1,2-Benzenediol, 3,5-bis(1,1-dimethylethyl)-(1020-31-1)
EPA Substance Registry System
1,2-Benzenediol, 3,5-bis(1,1-dimethylethyl)- (1020-31-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
10-23
TSCA 
Yes
HS Code 
29072900

MSDS

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3,5-Di-tert-butylcatechol Usage And Synthesis

Chemical Properties

white to pale brown solid

Uses

It is an important raw material and intermediate used in organic synthesis, Pharmaceuticals, agrochemicals and dyestuffs.

Purification Methods

Recrystallise the catechol from pet ether. [ Ley & Müller Chem Ber 89 1402 1956, UV Flaig et al. Z Naturforschung 10b 668 1955.] Also purify it by crystallising three times from pentane [Funabiki et al. J Am Chem Soc 108 2921 1986].

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