Guaiacol is a monomethoxybenzene that consists of phenol with a methoxy substituent at the ortho position.
Definition
Guaiacol is a monomethoxybenzene that consists of phenol with a methoxy substituent at the ortho position. It has a role as a disinfectant, a plant metabolite, an expectorant and an EC 1.1.1.25 (shikimate dehydrogenase) inhibitor. It is functionally related to a catechol.
Source: PubChem
US FDA substance register · UNII 6JKA7MAH9C · registered name Guaiacol · single chemical substance
Cosmetic roles
Safety & regulatory references
Not classified under Korea’s toxic-substance GHS list · existing chemical substance
More data — names, identifiers, properties, test records, literature
Names & identifiers
- CAS No.chemical registry number
- 90-05-1
- EC No.EU chemical inventory number
- 201-964-7
- DTXSIDUS EPA chemical ID
- DTXSID0023113
- DTXCIDUS EPA compound ID
- DTXCID003113
- IUPAC
- 2-Methoxyphenol
- Molecular formula
- C7H8O2
- Molecular weight
- 124.139 g/mol
Measured properties
- Appearance
- O-methoxyphenol appears as colorless to amber crystals or liquid. Density (of solid) 1.129 g / cm3. Solidifies at 28 °C (82.4 °F), but may remain liquid for a long time even at a much lower temperature. Slightly water soluble. Soluble in aqueous sodium hydroxide. Used medicinally as an expectorant. Used, because of its anti-oxidant properties, as an anti-skinning agent for paints. · Other Solid
- Odour
- Aromatic odor · CHARACTERISTIC SWEET ODOR, SLIGHTLY PHENOLIC
- Boiling point
- 399 to 403 °F at 760 mmHg (NTP, 1992) · 205 °C
- Melting point
- SOLIDIFIES at 82.4 °F (NTP, 1992) · 32 °C
- Solubility
- Slightly soluble (NTP, 1992) · Soluble in carbon tetrachloride
- Density
- 1.13 at 70.5 °F (NTP, 1992) - Denser than water, will sink · 1.1287 g/cu cm at 21 °C
- Stability
- Darkens on exposure to air and light
- Dissociation constant
- pKa = 9.98
- Colour
- WHITE OR SLIGHTLY YELLOW CRYSTALLINE MASS OR COLORLESS TO YELLOWISH
- Melting/freezing point
- 28 ℃
- Initial boiling point and range
- 205 ℃(1013 hPa)
- Flash point
- 82 ℃
- Vapour pressure
- 0.1027584 ㎜Hg (0.137 hPa at 25 deg c)
- Water solubility
- 15000 ㎎/ℓ (20 deg c)
- Relative density
- 1.097 (25 deg c(relative density))
- n-Octanol/water partition coefficient (Kow)
- 1.32
- Auto-ignition temperature
- 750 ℃
- Molecular weight
- 124.13
Values measured on the substance itself. The KOSHA data are a reference for writing and reviewing safety data sheets, not a specification for a commercial raw material.
Source: PubChem · KOSHA safety data sheets (Korea)
What products actually use it for
What the 8 products reported to the US EPA with this ingredient use it for. Products outside cosmetics are included, so the top few rows are its main uses.
- Fragrance3
- Intermediate2
- Flavouring and nutrient2
- No specific technical function1
Source: US EPA CompTox dashboard
Irritation and sensitisation studies
5 skin studies and 4 eye studies are on record.
The study conclusions largely agree (100%). These tests are on the raw material itself; irritation at the amount in a finished product is a different question.
See all 9 studies
- Not classified
Skin Irritation · Screening - Classification not possible
Skin Sensitization · Screening - Skin Irrit. 2
Skin Irritation · Authoritative - Category 6.3A (Category 2)
Skin Irritation · Read Across - Moderate or Mild Irritation
skin irritation: in vivo · Screening · OECD Guideline 404 (Acute Dermal Irritation / Corrosion) according to - Category 1
Eye Irritation · Screening - Eye Irrit. 2
Eye Irritation · Authoritative - Moderate or Mild Irritation
eye irritation: in vivo · Screening · OECD Guideline 405 (Acute Eye Irritation / Corrosion) according to - Category 6.4A (Category 2A)
Eye Irritation · Read Across
Source: US EPA CompTox dashboard
Related literature
- Orthonasal bioactive volatiles and their effects on salivation: a pilot study · 2026
- Direct Affinity-Immobilized Phenolic Acid Decarboxylase by a Linker Peptide on Zeolite for Efficient Bioconversion of Ferulic Acid into 4-Vinylguaiacol · 2020
- Analgesic Activity of Novel GABA Esters after Transdermal Delivery · 2016
- Synthesis and Pharmacological Properties of Novel Esters Based on Monocyclic Terpenes and GABA · 2016
- Outlooks on Medicinal Properties of Eugenol and its Synthetic Derivatives · 2016
Linked databases 15
- Australian Industrial Chemicals Inventory (AICIS)
- ChEBI
- ChEMBL
- EU CosIng ingredient list 2
- Korea toxic substances GHS register (NIER)
- KOSHA safety data sheets (Korea)
- NIST Chemistry WebBook
- PubChem 2
- Tlooto literature search 2 3 4 5
- US EPA CompTox dashboard 2
- US EPA DSSTox chemical database
- US FDA substance registration (GSRS)
- US FDA Unique Ingredient Identifier (UNII)
- Wikidata
- Wikipedia · English · Japanese · Chinese