88-58-4,MFCD00008825
Catalog No.:AA0032XV

88-58-4 | 2,5-Di-tert-butylhydroquinone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$6.00   $4.00
- +
25g
98%
in stock  
$13.00   $9.00
- +
100g
98%
in stock  
$19.00   $13.00
- +
500g
>98.0%(GC)
in stock  
$74.00   $52.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032XV
Chemical Name:
2,5-Di-tert-butylhydroquinone
CAS Number:
88-58-4
Molecular Formula:
C14H22O2
Molecular Weight:
222.3233
MDL Number:
MFCD00008825
SMILES:
CC(c1cc(O)c(cc1O)C(C)(C)C)(C)C
Properties
Properties
 
BP:
334.4 °C at 760 mmHg  
Form:
Solid  
MP:
216-218 °C(lit.)  
Refractive Index:
1.4576 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
208  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.6  

Upstream Synthesis Route

[1]Patent:US2002/68756,2002,A1,

[1]JournalofMolecularCatalysisA:Chemical,2013,vol.380,p.84-89

[2]ChineseJournalofCatalysis,2014,vol.35,#11,p.1874-1882

[1]AppliedCatalysisA:General,2013,vol.450,p.34-41

[1]AustralianJournalofChemistry,1997,vol.50,#5,p.515-516

[1]BulletinoftheChemicalSocietyofJapan,1991,vol.64,#1,p.336-338

[2]OrganicandBiomolecularChemistry,2009,vol.7,#7,p.1445-1453

[3]Synthesis,2012,vol.44,#8,p.1183-1189

[4]Tetrahedron,1987,vol.43,#17,p.3963-3974

[5]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1981,p.2970-2973

[6]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1982,p.509-511

[7]Tetrahedron,1987,vol.43,#17,p.3963-3974

[8]SyntheticCommunications,2006,vol.36,#12,p.1751-1759

[9]JournalofOrganicChemistry,2000,vol.65,#24,p.8391-8394

[10]Tetrahedron,2013,vol.69,#40,p.8612-8617

[11]Synthesis(Germany),2015,vol.47,#20,p.3207-3211

[12]Synthesis,1985,#6/7,p.641-643

[13]Tetrahedron,1993,vol.49,#1,p.105-112

[14]AdvancedSynthesisandCatalysis,2005,vol.347,#4,p.517-520

[15]Chemistry-AEuropeanJournal,2014,vol.20,#32,p.9914-9917

[16]Tetrahedron,1987,vol.43,#8,p.1753-1758

[17]SyntheticCommunications,1980,vol.10,#8,p.615-622

[18]SyntheticCommunications,1980,vol.10,#8,p.615-622

[19]Tetrahedron,1986,vol.42,#8,p.2319-2324

[20]PolishJournalofChemistry,2007,vol.81,#5-6,p.1049-1061

[21]OrganicandBiomolecularChemistry,2006,vol.4,#2,p.200-202

[22]TetrahedronLetters,1994,vol.35,#28,p.5083-5084

[23]TetrahedronLetters,1988,vol.29,#22,p.2671-2674

[24]JournaloftheAmericanChemicalSociety,2002,vol.124,#41,p.12261-12267

[25]JournalofOrganicChemistry,1987,vol.52,#22,p.5053-5055

[26]BulletinoftheChemicalSocietyofJapan,1995,vol.68,#6,p.1655-1660

[27]Synthesis,1980,#9,p.706-708

[28]SyntheticCommunications,1989,vol.19,#7,8,p.1317-1324

[29]JustusLiebigsAnnalenderChemie,1955,vol.597,p.196,211

[30]ActaChemicaScandinavica(1947-1973),1953,vol.7,p.938,939

[31]Patent:US2577505,1950,,

[32]JournaloftheChemicalSociety,1952,p.4666,4674

[33]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1057,1063

[34]ChemistryLetters,1976,p.1293-1296

[35]JournalofOrganicChemistry,1983,vol.48,#24,p.4764-4766

[36]ZeitschriftfuerPhysikalischeChemie(Leipzig),1989,vol.270,#5,p.887-896

[37]JournalofOrganicChemistry,1981,vol.46,#22,p.4545-4551

[38]CanadianJournalofChemistry,1986,vol.64,p.225-231

[39]JournalofOrganicChemistry,1981,vol.46,#16,p.3215-3218

[40]JournalofOrganicChemistry,1981,vol.46,#16,p.3215-3218

[41]JournaloftheAmericanChemicalSociety,1980,vol.102,#15,p.4999-5004

[42]JournaloftheAmericanChemicalSociety,1980,vol.102,#15,p.4999-5004

[43]Patent:EP812816,1997,A1,

Downstream Synthesis Route
108-31-6    14296-80-1    88-58-4    71-43-2   
1,2,3,4,5,6-hexahydro-cyclobutabenzene-4<i>r</i>,5<i>c</i>-dicarboxylicacid-anhydride 

[1]JournaloftheAmericanChemicalSociety,1956,vol.78,p.109,111

[1]JournalofOrganicChemistry,2019,vol.84,p.13655-13664

[2]JournaloftheAmericanChemicalSociety,1980,vol.102,p.3774-3783

[3]Tetrahedron,1993,vol.49,p.105-112

[4]AsianJournalofChemistry,2010,vol.22,p.2549-2553

[5]Polyhedron,2018,vol.143,p.209-214

[6]JournaloftheAmericanChemicalSociety,1952,vol.74,p.4087

[1]BulletinoftheChemicalSocietyofJapan,1991,vol.64,p.336-338

[2]OrganicandBiomolecularChemistry,2009,vol.7,p.1445-1453

[3]Synthesis,2012,vol.44,p.1183-1189

[4]Tetrahedron,1987,vol.43,p.3963-3974

[5]JournaloftheChemicalSociety.PerkintransactionsI,1981,p.2970-2973

[6]JournaloftheChemicalSociety.PerkintransactionsI,1982,p.509-511

[7]Tetrahedron,1987,vol.43,p.3963-3974

[8]SyntheticCommunications,2006,vol.36,p.1751-1759

[9]JournalofOrganicChemistry,2000,vol.65,p.8391-8394

[10]Tetrahedron,2013,vol.69,p.8612-8617

[11]Synthesis,2015,vol.47,p.3207-3211

[12]Synthesis,1985,p.641-643

[13]Tetrahedron,1993,vol.49,p.105-112

[14]AdvancedSynthesisandCatalysis,2005,vol.347,p.517-520

[15]Chemistry-AEuropeanJournal,2014,vol.20,p.9914-9917

[16]Tetrahedron,1987,vol.43,p.1753-1758

[17]SyntheticCommunications,1980,vol.10,p.615-622

[18]SyntheticCommunications,1980,vol.10,p.615-622

[19]Tetrahedron,1986,vol.42,p.2319-2324

[20]PolishJournalofChemistry,2007,vol.81,p.1049-1061

[21]OrganicandBiomolecularChemistry,2006,vol.4,p.200-202

[22]TetrahedronLetters,1994,vol.35,p.5083-5084

[23]TetrahedronLetters,1988,vol.29,p.2671-2674

[24]JournaloftheAmericanChemicalSociety,2002,vol.124,p.12261-12267

[25]JournalofOrganicChemistry,1987,vol.52,p.5053-5055

[26]BulletinoftheChemicalSocietyofJapan,1995,vol.68,p.1655-1660

[27]Synthesis,1980,p.706-708

[28]SyntheticCommunications,1989,vol.19,p.1317-1324

[29]JustusLiebigsAnnalenderChemie,1955,vol.597,p.196,211

[30]ActaChemicaScandinavica(1947),1953,vol.7,p.938,939

[31]JournaloftheChemicalSociety,1952,p.4666,4674

[32]JournaloftheAmericanChemicalSociety,1947,vol.69,p.1057,1063

[33]ChemistryLetters,1976,p.1293-1296

[34]JournalofOrganicChemistry,1983,vol.48,p.4764-4766

[35]ZeitschriftfurPhysikalischeChemie(Leipzig),1989,vol.270,p.887-896

[36]JournalofOrganicChemistry,1981,vol.46,p.4545-4551

[37]CanadianJournalofChemistry,1986,vol.64,p.225-231

[38]JournalofOrganicChemistry,1981,vol.46,p.3215-3218

[39]JournalofOrganicChemistry,1981,vol.46,p.3215-3218

[40]JournaloftheAmericanChemicalSociety,1980,vol.102,p.4999-5004

[41]JournaloftheAmericanChemicalSociety,1980,vol.102,p.4999-5004

[42]Patent:EP812816,1997,A1

[43]DaltonTransactions,2019,vol.48,p.6445-6454

[1]JournalofChemicalPhysics,1958,vol.28,p.774

[2]JournaloftheAmericanChemicalSociety,2003,vol.125,p.8318-8329

[3]JournaloftheAmericanChemicalSociety,2003,vol.125,p.8318-8329

[4]AngewandteChemie-InternationalEdition,2009,vol.48,p.8348-8351

[1]JournaloftheAmericanChemicalSociety,1980,vol.102,p.4999-5004

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SDS
Tags:88-58-4 Molecular Formula|88-58-4 MDL|88-58-4 SMILES|88-58-4 2,5-Di-tert-butylhydroquinone
Catalog No.: AA0032XV
88-58-4,MFCD00008825
88-58-4 | 2,5-Di-tert-butylhydroquinone
Pack Size: 100mg
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 25g
Purity: 98%
in stock
$13.00 $9.00
Pack Size: 100g
Purity: 98%
in stock
$19.00 $13.00
Pack Size: 500g
Purity: >98.0%(GC)
in stock
$74.00 $52.00
Quantity
- +
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Technical Information
Catalog Number: AA0032XV
Chemical Name: 2,5-Di-tert-butylhydroquinone
CAS Number: 88-58-4
Molecular Formula: C14H22O2
Molecular Weight: 222.3233
MDL Number: MFCD00008825
SMILES: CC(c1cc(O)c(cc1O)C(C)(C)C)(C)C
Properties
BP: 334.4 °C at 760 mmHg  
Form: Solid  
MP: 216-218 °C(lit.)  
Refractive Index: 1.4576 (estimate)  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 208  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.6  
Upstream Synthesis Route
637-81-0    88-58-4    6630-33-7    103858-52-2 

[1]Patent:US2002/68756,2002,A1,

123-31-9    75-65-0    6669-13-2    2460-77-7    88-58-4    1948-33-0 

[1]JournalofMolecularCatalysisA:Chemical,2013,vol.380,p.84-89

[2]ChineseJournalofCatalysis,2014,vol.35,#11,p.1874-1882

1634-04-4    123-31-9    2444-28-2    88-58-4    2460-87-9    1948-33-0 

[1]AppliedCatalysisA:General,2013,vol.450,p.34-41

123-31-9    115-11-7    88-58-4    2467-52-9    1948-33-0 

[1]AustralianJournalofChemistry,1997,vol.50,#5,p.515-516

88-58-4    2460-77-7 

[1]BulletinoftheChemicalSocietyofJapan,1991,vol.64,#1,p.336-338

[2]OrganicandBiomolecularChemistry,2009,vol.7,#7,p.1445-1453

[3]Synthesis,2012,vol.44,#8,p.1183-1189

[4]Tetrahedron,1987,vol.43,#17,p.3963-3974

[5]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1981,p.2970-2973

[6]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1982,p.509-511

[7]Tetrahedron,1987,vol.43,#17,p.3963-3974

[8]SyntheticCommunications,2006,vol.36,#12,p.1751-1759

[9]JournalofOrganicChemistry,2000,vol.65,#24,p.8391-8394

[10]Tetrahedron,2013,vol.69,#40,p.8612-8617

[11]Synthesis(Germany),2015,vol.47,#20,p.3207-3211

[12]Synthesis,1985,#6/7,p.641-643

[13]Tetrahedron,1993,vol.49,#1,p.105-112

[14]AdvancedSynthesisandCatalysis,2005,vol.347,#4,p.517-520

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[16]Tetrahedron,1987,vol.43,#8,p.1753-1758

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Downstream Synthesis Route
108-31-6    14296-80-1    88-58-4    71-43-2   
1,2,3,4,5,6-hexahydro-cyclobutabenzene-4<i>r</i>,5<i>c</i>-dicarboxylicacid-anhydride 

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