3,5-Di-t-butylcatechol

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Names

[ CAS No. ]:
1020-31-1

[ Name ]:
3,5-Di-t-butylcatechol

[Synonym ]:
4,6-Di-tert-butylpyrocatechol
3,5-Di-tert-butylpyrocatechol
3,5-DI-TERT-BUTYCATECHOL
3,5-DI-TERTIO-BUTYLCATECHOL
3,5-di-tert-butyl-catechol
MFCD00008819
1,2-Benzenediol, 3,5-di(1,1-dimethylethyl)-
3,5-Bis(2-methyl-2-propanyl)-1,2-benzenediol
3,5-di-tert-butyl-pyrocatechin
1,2-Benzenediol, 3,5-bis(1,1-dimethylethyl)-
3,5-Di-tert-butylcatechol
DI-3,5-TERT-BUTYLCATECHOL
1,2-dihydroxy-3,5-di-tert-butyl benzene
3,5-Di-tert-butylbenzene-1,2-diol
Pyrocatechol, 3,5-di-tert-butyl-
3,5-DI-TERT-BUTYHLCATECHOL
3,5-DTBC
3,5-DTBC-H2
3,5-Di-t-butylcatechol
EINECS 213-816-9

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
309.7±37.0 °C at 760 mmHg

[ Melting Point ]:
95-100 °C(lit.)

[ Molecular Formula ]:
C14H22O2

[ Molecular Weight ]:
222.323

[ Flash Point ]:
136.5±21.1 °C

[ Exact Mass ]:
222.161987

[ PSA ]:
40.46000

[ LogP ]:
4.26

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.520

[ Storage condition ]:
2~8℃

[ Stability ]:
Stable. Combustible. Incompatible with strong oxidizing agents.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29072900

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1,2-Benzenediol
  • tert-Butanol
  • 1,3,5-Tri-tert-butylbenzene
  • 2,4,6,8-tetraiodo-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione
  • Isobutylene
  • 2-Bromo-2-methylpropane
  • 3,5-DI-TERT-BUTYL-O-BENZOQUINONE
  • 2,4-Di-t-butylphenol
  • 7,9-di-tert-butyl-2,5-epoxybenzo[e][1,2,4,7]tetraoxocine

DownStream

  • 5,7-ditert-butyl-1,4-benzodioxine
  • 4,6-ditert-butyl-1,3-benzodioxole
  • 5,7-ditert-butyl-2,3-dihydro-1,4-benzodioxine
  • 2,7-Oxepindione,3,5-bis(1,1-dimethylethyl)-
  • 3,5-DI-TERT-BUTYL-O-BENZOQUINONE
  • 3,5-ditert-butyl-4-hydroxycyclohexa-3,5-diene-1,2-dione
  • 3,5-di-tert-butyl-5-(formyl)-2-furanone
  • 3,5-ditert-butylpyran-2-one
  • tert-Butylmaleinsaeureanhydrid

Customs

[ HS Code ]: 2907299090

[ Summary ]:
2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0%

Articles

Catechol oxidase activity of a series of new dinuclear copper(II) complexes with 3,5-DTBC and TCC as substrates: syntheses, X-ray crystal structures, spectroscopic characterization of the adducts and kinetic studies.

Inorg. Chem. 47(16) , 7083-93, (2008)

A series of dinuclear copper(II) complexes has been synthesized with the aim to investigate their applicability as potential structure and function models for the active site of catechol oxidase enzym...

3,5-Di-t-butyl catechol is a potent human ryanodine receptor 1 activator, not suitable for the diagnosis of malignant hyperthermia susceptibility.

Pharmacol. Res. 66(1) , 80-7, (2012)

3,5-Di-t-butyl catechol (DTCAT) releases Ca(2+) from rat skeletal muscle sarcoplasmic reticulum (SR) vesicles. Hence, it is a candidate for use as a substitute for halothane or caffeine in the in vitr...

A novel tripodal ligand containing three different N-heterocyclic donor functions and its application in catechol dioxygenase mimicking.

Chemistry 15(22) , 5567-76, (2009)

We describe a novel chiral ligand, L, in which three different N-donor functions are linked to a methoxymethine unit: a methylpyrazole derivative, a methylimidazole unit, and a pyridyl residue. Comple...


More Articles

Related Compounds

  • 3,5-Di-t-butylcatechol
  • 3,5-di-t-butylcatechol
  • sodium 3,5-di-t-butylcatecholate
  • 3,5-di-t-butyl-1,2-benzoquinone 1-monoxime
  • 3,5-di-t-Butyl-4-hydroxyanisole
  • 3,5-Di-t-butyl-2,4-dinitroanilin
  • 4-[4-(3-Bromophenyl)piperazin-1-yl]pyridine-2-carboxamide
  • N-tert-butyl-1-(9H-purin-6-yl)pyrrolidine-3-carboxamide
  • 5-fluoro-N-(1-methyl-1H-pyrazol-3-yl)pyridine-3-carboxamide
  • 5-Methyl-4-(4-{[2-(trifluoromethyl)phenyl]methyl}piperazin-1-yl)pyrimidine
  • 3-(2-Methoxyethyl)-1-[1-(quinoxalin-2-yl)piperidin-4-yl]imidazolidine-2,4-dione
  • 2-cyclopropyl-N-[(2-fluorophenyl)methyl]-6-(oxan-4-yl)pyrimidin-4-amine
  • 2-Tert-butyl-4,5-dimethyl-6-({1-[(3-methyl-1,2,4-oxadiazol-5-yl)methyl]piperidin-4-yl}methoxy)pyrimidine
  • 1-[1-(6-Chloro-1,3-benzothiazol-2-yl)piperidin-4-yl]-3-(2-methoxyethyl)imidazolidine-2,4-dione
  • N-methyl-N-[1-[(3-methyl-1,2,4-oxadiazol-5-yl)methyl]pyrrolidin-3-yl]-1,1-dioxo-1,2-benzothiazol-3-amine
  • 2-[3-(Fluoromethyl)piperidin-1-yl]-4-methyl-1,3-benzothiazole
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