95-71-6 | Methylhydroquinone

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$16.00	$11.00
5g	95%	in stock	$20.00	$14.00
25g	95%	in stock	$25.00	$17.00
100g	95%	in stock	$38.00	$26.00
500g	95%	in stock	$185.00	$130.00

Description

• Catalog Number: AB62718
• Chemical Name: Methylhydroquinone
• CAS Number: 95-71-6
• Molecular Formula: C7H8O2
• Molecular Weight: 124.13722000000001
• MDL Number: MFCD00002345
• SMILES: Oc1ccc(c(c1)C)O
• NSC Number: 4962

Computed Properties

• Complexity: 92.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1

Literature

• Methanogenic toluene metabolism: community structure and intermediates.

  Environmental microbiology 20120301

• Metabolism of 2-chloro-4-nitrophenol in a gram negative bacterium, Burkholderia sp. RKJ 800.

  PloS one 20120101

• Solar photoelectro-Fenton degradation of the herbicide 4-chloro-2-methylphenoxyacetic acid optimized by response surface methodology.

  Journal of hazardous materials 20111030

• Formation of efficient catalytic silver nanoparticles on carbon nanotubes by adenine functionalization.

  Angewandte Chemie (International ed. in English) 20111010

• Natural compounds containing a catechol group enhance the formation of Nε-(carboxymethyl)lysine of the Maillard reaction.

  Free radical biology & medicine 20110401

• Genopal™: a novel hollow fibre array for focused microarray analysis.

  DNA research : an international journal for rapid publication of reports on genes and genomes 20101201

• Theoretical study on the thermodynamic properties and self-decomposition of methylbenzenediol isomers.

  The journal of physical chemistry. A 20101104

• Gentisides C-K: nine new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch.

  Bioorganic & medicinal chemistry 20101001

• The redox-sensing regulator YodB senses quinones and diamide via a thiol-disulfide switch in Bacillus subtilis.

  Proteomics 20100901

• Biosynthesis and toxicological effects of patulin.

  Toxins 20100401

• Gentisides A and B, two new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch.

  Bioorganic & medicinal chemistry 20100315

• Genotoxic and Cytotoxic Safety Evaluation of Papain (Carica papaya L.) Using In Vitro Assays.

  Journal of biomedicine & biotechnology 20100101

• Differences in defensive volatiles of the forked fungus beetle, Bolitotherus cornutus, living on two species of fungus.

  Journal of chemical ecology 20091101

• Synthesis, characterization and texture observations of calamitic liquid crystalline compounds.

  International journal of molecular sciences 20091101

• [Decolorization of azo dyes using quinone reductase and quinoid compounds].

  Huan jing ke xue= Huanjing kexue 20090615

• Acceleration of azo dye decolorization by using quinone reductase activity of azoreductase and quinone redox mediator.

  Bioresource technology 20090601

• Molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus.

  Microbiology (Reading, England) 20090501

• Electrochemical incineration of cresols: a comparative study between PbO2 and boron-doped diamond anodes.

  Chemosphere 20090301

• Complementary cooperation between two syntrophic bacteria in pesticide degradation.

  Journal of theoretical biology 20090221

• Simple ortho- and para-hydroquinones as compounds neuroprotective against oxidative stress in a manner associated with specific transcriptional activation.

  Biochemical and biophysical research communications 20090206

• Transcriptome and proteome analyses of adaptive responses to methyl methanesulfonate in Escherichia coli K-12 and ada mutant strains.

  BMC microbiology 20090101

• Regulation of quinone detoxification by the thiol stress sensing DUF24/MarR-like repressor, YodB in Bacillus subtilis.

  Molecular microbiology 20080301

• Proteomic signatures uncover thiol-specific electrophile resistance mechanisms in Bacillus subtilis.

  Expert review of proteomics 20080201

• 2,5-dihydroxybenzyl and (1,4-dihydroxy-2-naphthyl)methyl, novel reductively armed photocages for the hydroxyl moiety.

  The Journal of organic chemistry 20071123

• The MarR-type repressor MhqR (YkvE) regulates multiple dioxygenases/glyoxalases and an azoreductase which confer resistance to 2-methylhydroquinone and catechol in Bacillus subtilis.

  Molecular microbiology 20071001

• Transcriptome and proteome analyses in response to 2-methylhydroquinone and 6-brom-2-vinyl-chroman-4-on reveal different degradation systems involved in the catabolism of aromatic compounds in Bacillus subtilis.

  Proteomics 20070501

• Pharmacologically active natural products in the defence secretion of Palembus ocularis (Tenebrionidae, Coleoptera).

  Journal of ethnopharmacology 20060615

• Isolation of fenitrothion-degrading strain Burkholderia sp. FDS-1 and cloning of mpd gene.

  Biodegradation 20060601

• p-hydroxylation reactions catalyzed by naphthalene dioxygenase.

  FEMS microbiology letters 20060201

• Alanine 101 and alanine 110 of the alpha subunit of Pseudomonas stutzeri OX1 toluene-o-xylene monooxygenase influence the regiospecific oxidation of aromatics.

  Biotechnology and bioengineering 20051205

• Characterization of methylhydroquinone-metabolizing oxygenase genes encoded on plasmid in Burkholderia sp. NF100.

  Journal of bioscience and bioengineering 20051101

• Nitric oxide promotes strong cytotoxicity of phenolic compounds against Escherichia coli: the influence of antioxidant defenses.

  Free radical biology & medicine 20031201

• Oxidative DNA damage induced by toluene is involved in its male reproductive toxicity.

  Free radical research 20030101

• Vibrational analysis of substituted phenols: part I. Vibrational spectra, normal coordinate analysis and transferability of force constants of some formyl-, methoxy-, formylmethoxy-, methyl- and halogeno-phenols.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20021201

• Characterization of manganese-dependent peroxidase isoenzymes from the ligninolytic fungus Phanerochaete flavido-alba.

  Research in microbiology 20021001

• Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds.

  Antiviral chemistry & chemotherapy 20020701

• Volatile components in dorsal gland secretions of the white-lipped peccary, Tayassu pecari, from Bolivia.

  Journal of chemical ecology 20011201

• Dioxygenative cleavage of C-methylated hydroquinones and 2,6-dichlorohydroquinone by Pseudomonas sp. HH35.

  Biochimica et biophysica acta 20011107

• Studies of all-trans-retinal as a photooxidizing agent.

  Photochemistry and photobiology 20010101

• Selective inhibitory activity of polyhydroxycarboxylates derived from phenolic compounds against human immunodeficiency virus replication.

  Journal of acquired immune deficiency syndromes 19910101

• Patulin biosynthesis: epoxidation of toluquinol and gentisyl alcohol by particulate preparations from Penicillium patulum.

  Biochemistry 19891114