Guaiacol

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Suppliers

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  1 Kg
  $29.00

  5 Kg
  $116.00

Most-cited Publications

• Catechol-O-Methyl Transferase: Pharmacological Aspects and Physiological Role (Pharmacological Reviews, 1975)
• Separate Assays Specific for Ascorbate Peroxidase and Guaiacol Peroxidase and for the Chloroplastic and Cytosolic Isozymes of Ascorbate Peroxidase in Plants (Plant and Cell Physiology, 1994)
• Hydrodeoxygenation of guaiacol as model compound for pyrolysis oil on transition metal phosphide hydroprocessing catalysts (Applied Catalysis A-general, 2011)
• Hydrodeoxygenation of guaiacol on noble metal catalysts (Catalysis Today, 2009)
• Influence of the Support of CoMo Sulfide Catalysts and of the Addition of Potassium and Platinum on the Catalytic Performances for the Hydrodeoxygenation of Carbonyl, Carboxyl, and Guaiacol-Type Molecules (Journal of Catalysis, 1995)
• Hydrodeoxygenation of guaiacol with CoMo catalysts. Part I: Promoting effect of cobalt on HDO selectivity and activity (Applied Catalysis B-environmental, 2011)

Areas of Application

Safety

• Request a Demo
  Predict GHS Hazards for Any Chemical in silico.
  Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.
• H302: Harmful if swallowed
  Warning Acute toxicity, oral - Category 4
• H319: Causes serious eye irritation
  Warning Serious eye damage/eye irritation - Category 2A
• H332: Harmful if inhaled
  Warning Acute toxicity, inhalation - Category 4
• H350: May cause cancer
  Danger Carcinogenicity - Category 1A, 1B
• H402: Harmful to aquatic life
  Hazardous to the aquatic environment, acute hazard - Category 3

Trends

Alternate Names

• Methyl Catechol
• Guaicol
• 2-Hydroxyanisole
• 2-Hydroxy-Anisole
• 2-Methoxyphenol
• 2-Methoxy-Phenol
• SMILES
  COC1=CC=CC=C1O
• InChIKey
  LHGVFZTZFXWLCP-UHFFFAOYSA-N

External Links

• Pubchem - Guaiacol
• Wikipedia - guaiacol
  Guaiacol is a naturally occurring organic compound with the formula C6H4(OH)(OCH3), first isolated by Otto Unverdorben in 1826. Although it is biosynthesized by a variety of organisms, this yellowish aromatic oil is usually derived from guaiacum or wood creosote. Samples darken upon exposure to air and light.

Synthesis

SALICYLALDEHYDE  +  Methyl hydroperoxide (Dakin oxidation)

Synthesis of Guaiacol ›

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2-Ethoxyphenol (94-71-3)

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2,6-DIMETHOXYPHENOL (91-10-1)

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2,3-Dimethoxyphenol (25155-26-4, 5150-42-5)

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3,4-DIMETHOXYPHENOL (2033-89-8)

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1,2,3-TRIMETHOXYBENZENE (634-36-6, 63744-60-5)

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1,3-BENZODIOXOLE (274-09-9)

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1,3,5-Trimethoxybenzene (621-23-8)

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2-(2-Ethoxyphenoxy)-N-methylethanamine (6660-49-7)

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1-(2-Chloroethoxy)-2-isopropoxybenzene (915921-87-8)

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PHENETOLE (103-73-1)

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3,4-Dimethoxyaniline (6315-89-5)

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DIBENZO-18-CROWN-6 (14187-32-7)

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[3-(2-methoxyphenoxy)propyl]methylamine hydrochloride (1609407-81-9)

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2-(2-CHLOROETHOXY)-1,3-DIMETHOXYBENZENE (24251-50-1)

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4-Ethoxyphenol (622-62-8)

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2-Methoxy-6-methylphenol (2896-67-5)

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1-(2-methoxyphenoxy)-2-propanamine (6505-08-4)

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2,3-dihydrobenzo[b][1,4]dioxin-6-ol (10288-72-9)

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2,3-Dihydro-1,4-benzodioxin-5-ol (10288-36-5)

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2,6-Dimethoxynaphthalene (5486-55-5)

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Phenoxyacetonitrile (3598-14-9)

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Guaiacol

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