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Merck
CN

D45800

3,5-Di-tert-butylcatechol

98%

Synonym(s):

3,5-Bis(1,1-dimethylethyl)-1,2-benzenediol, 3,5-Di-tert-Butyl-1,2-Hydroxybenzene, 3,5-Di-tert-butyl-1,2-benzenediol, 3,5-Di-tert-butyl-1,2-dihydroxybenzene, 3,5-Di-tert-butyl-o-hydroquinone, 3,5-Di-tert-butylpyrocatechol, 3,5-Ditert-butylbenzene-1,2-diol, 4,6-Di-tert-butyl-1,2-benzenediol, 4,6-Di-tert-butylpyrocatechol

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About This Item

Linear Formula:
[(CH3)3C]2C6H2-1,2-(OH)2
CAS Number:
1020-31-1
Molecular Weight:
222.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893886
EC Number:
213-816-9
Beilstein/REAXYS Number:
1370212
MDL number:
MFCD00008819

Key Documents

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Product Name

3,5-Di-tert-butylcatechol, 98%

InChI

1S/C14H22O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8,15-16H,1-6H3

InChI key

PJZLSMMERMMQBJ-UHFFFAOYSA-N

SMILES string

CC(C)(C)c1cc(O)c(O)c(c1)C(C)(C)C

assay

98%

form

crystals

mp

95-100 °C (lit.)

Quality Level

100

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Application

3,5-Di-tert-butylcatechol can be used as:
  • A reactant to prepare 3,5-di-tert-butylquinone via catalytic oxidation.
  • A polymerization inhibitor in the production of monomers such as styrene and butadiene.
  • An additive in the synthesis of enantioselective 1,2-oxazinanes, and isoxazolidines via asymmetric nitroso aldol reaction using L-proline as a catalyst.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000325019
0000325019
MKCW1998
MKCT8359
MKCS8254

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Mehmet Tümer et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(3-4), 916-929 (2006-10-19)
In this study, we synthesized the amine compound 2-(2-aminoethyliminomethyl)phenol (H(3)A) as the starting material, and then we prepared the polydentate Schiff base ligands from the reactions of the amine compound (H(3)A) with phtaldialdehyde (H(2)L), 4-methyl-2,6-di-formlyphenol (H(3)L(1)) and 4-t-butyl-2,6-di-formylphenol (H(3)L(2)) in
C H Kao et al.
Journal of inorganic biochemistry, 84(3-4), 171-178 (2001-05-26)
Eight oxy-bridged dinuclear copper(II) complexes with catecholase-like sites, [Cu(L1)X]2 (HL1 = 1-diethylaminopropan-2-ol, X=N3- 1, NCO- 2, and NO2- 3), [Cu(L2)X]2 (HL2=N-ethylsalicylaldimine, X=NO3- 4, Cl- 5, N3- 6, NCS- 7), and [Cu(L3)]2(ClO4)2, 8 (HL3=N-(salicylidene)-N'-(2-pyridylaldene)propanediamine) have been prepared and characterized. The single
Apurba Biswas et al.
Inorganic chemistry, 51(15), 7993-8001 (2012-07-05)
Three double phenoxido-bridged dinuclear nickel(II) complexes, namely [Ni(2)(L(1))(2)(NCS)(2)] (1), [Ni(2)(L(2))(2)(NCS)(2)] (2), and [Ni(2)(L(3))(2)(NCS)(2)] (3) have been synthesized using the reduced tridentate Schiff-base ligands 2-[1-(3-methylamino-propylamino)-ethyl]-phenol (HL(1)), 2-[1-(2-dimethylamino-ethylamino)-ethyl]-phenol (HL(2)), and 2-[1-(3-dimethylamino-propylamino)-ethyl]-phenol (HL(3)), respectively. The coordination compounds have been characterized by X-ray structural
Christopher Grieco et al.
Faraday discussions, 216(0), 520-537 (2019-04-24)
Eumelanin is a natural pigment with photoprotective and radical scavenging characteristics, which are vital for a multitude of living organisms. However, the molecular mechanisms behind these functions remain obscure, in part because eumelanin is a heterogeneous polymer composed of a
Catalytic oxidation of 3, 5-di-tert-butylcatechol by a manganese (III) 18-azametallacrown-6 compound: Synthesis, crystal structure, fluorescence, magnetic and kinetic investigation
Majumder A, et al.
Inorganica chimica acta, 359(8), 2375-2382 (2006)
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