2,3-Dimethylhydroquinone

Product Information

Molecular Formula:
C8H10O2
Molecular Weight:
138.16
Description
Antioxidant
Synonyms
1,4-Benzenediol, 2,3-dimethyl-; Hydroquinone, 2,3-dimethyl-; o-Xylene-3,6-diol; o-Xylohydroquinone; 2,3-XYLOHYDROQUINONE; 2,3-DIMETHYLHYDROQUINONE; 2,3-DIMETHYLBENZENE-1,4-DIOL; 2,3-DIMETHYL-1,4-BENZENEDIOL
IUPAC Name
2,3-dimethylbenzene-1,4-diol
Canonical SMILES
CC1=C(C=CC(=C1C)O)O
InChI
InChI=1S/C8H10O2/c1-5-6(2)8(10)4-3-7(5)9/h3-4,9-10H,1-2H3
InChI Key
BXJGUBZTZWCMEX-UHFFFAOYSA-N
Boiling Point
170-175 °C/1 mmHg(lit.)
Flash Point
235.4 °F
Purity
98%
Appearance
powder
Refractive Index
n20/D 1.479 (lit.)

Computed Properties

XLogP3
1.2
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
138.068079557 g/mol
Monoisotopic Mass
138.068079557 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
99.8
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113956889-A Colored polysilsesquioxane liquid crystal film and preparation method and application thereof 2021-09-27
CN-113249116-A Fluorescent organic-inorganic silicon oxide liquid crystal material and preparation method thereof 2021-05-20
CN-113234193-A Self-supporting liquid crystal film and preparation method thereof 2021-05-20
CN-113249116-B Fluorescent organic-inorganic silicon oxide liquid crystal material and preparation method thereof 2021-05-20
KR-102242940-B1 Method for preparing a non-reducing cleaning composition containing vegetable extracts and a non-reducing cleaning composition prepared thereby 2021-01-19
CN-112500349-A Synthetic method of benzo lactam compound 2021-01-12
JP-2022036643-A Method for manufacturing polyarylene ether ketone 2020-08-24
CN-111848361-A Novel cyclotri-veratrum hydrocarbon analogue and derivative, preparation method and application thereof 2020-08-14
CN-111848361-B Novel cyclotri-veratrum hydrocarbon analogue and derivative, preparation method and application thereof 2020-08-14
WO-2022024054-A1 Odorants and compositions comprising odorants 2020-07-31

Literatures

PMID Publication Date Title Journal
21963628 2011-01-01 A new way for synthesis of phenoxazine and diphenoxazine derivatives via electrochemical method Chemical & pharmaceutical bulletin
21588235 2010-07-03 1,7-Dimethyl-penta-cyclo-[5.4.0.0.0.0]undecane-8,11-dione Acta crystallographica. Section E, Structure reports online
20052974 2010-02-05 Enantioselective total synthesis of the natural gamma-tocopherol metabolite (S)-gamma-CEHC [(S)-LLU-alpha] Organic letters
16497004 2006-03-03 Electrochemical oxidation of 2,3-dimethylhydroquinone in the presence of 1,3-dicarbonyl compounds The Journal of organic chemistry
12495212 2002-07-01 Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds Antiviral chemistry & chemotherapy
11767888 2001-11-01 An N,N'-dialkyl-4,4'-bipyridinium-modified titanium-dioxide photocatalyst for water remediation--observation and application of supramolecular effects in photocatalytic degradation of pi-donor organic compounds Fresenius' journal of analytical chemistry
11202369 2001-01-01 Studies of all-trans-retinal as a photooxidizing agent Photochemistry and photobiology
10994872 2000-01-01 Oxidation of hydroquinone, 2,3-dimethylhydroquinone and 2,3,5-trimethylhydroquinone by human myeloperoxidase Redox report : communications in free radical research
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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