Pyrocatechol (Catechol)
The consolidated GB Cosmetics Regulation lists this record in Annex II.
Regulatory decision and full conditions
- Status
- Prohibited
- Legal role
- Binding rule
- Regulatory summary
- The consolidated GB Cosmetics Regulation lists this record in Annex II.
- Conditions and restrictions
- A prohibition entry may contain no separate condition text because the regulatory outcome is the prohibition itself. Open the cited source and apply the market-wide requirements below.
Substance identity
- Official source name
- Pyrocatechol (Catechol)
- CAS
- 120-80-9
- EC
- 204-427-5
- Identity mapping
- cas_number
- Linked ingredient
- PYROCATECHOL
Linked CosIng identity data
Names and aliases
CosIng description: 1,2-Benzenediol
EU inventory restriction note: II/408
Recorded cosmetic function: HAIR DYEING
Function pages:HAIR DYEING
View the complete ingredient profileCross-market snapshot for this identity
Exact linked records currently present in this site. An absent market means no imported exact match, not permission to use the substance.
European Union
1 linked record
Open supporting recordGreat Britain
Current record1 linked record
Open supporting recordCanada
1 linked record · 1 with specific conditions
Open supporting recordNew Zealand
1 linked record
Open supporting recordASEAN
1 linked record
Open supporting recordChina
1 linked record · 1 with specific conditions
Open supporting recordSouth Korea
1 linked record
Open supporting recordBrazil
1 linked record · 1 with specific conditions
Open supporting recordIndia
1 linked record · 1 with specific conditions
Open supporting recordSaudi Arabia
1 linked record
Open supporting recordVerified chemistry for CAS 120-80-9
Catechol
Catechol is a benzenediol comprising of a benzene core carrying two hydroxy substituents ortho to each other. It has a role as a genotoxin, an allelochemical and a plant metabolite. It is a conjugate acid of a catecholate(1-). — ChEBI
- IUPAC name
- benzene-1,2-diol
- Molecular formula
- C6H6O2
- Molecular weight
- 110.11 g/mol
- Exact mass
- 110.036779430 Da
- Monoisotopic mass
- 110.036779430 Da
- XLogP3
- 0.9
- Topological polar surface area
- 40.5 Ų
- Molecular complexity
- 62.0
- Formal charge
- 0
- Hydrogen-bond donors
- 2
- Hydrogen-bond acceptors
- 2
- Rotatable bonds
- 0
- Heavy atoms
- 8
- Covalent units
- 1
Names and synonyms reported to PubChem
16 more reported names
External database identifiers
- ChEBI:CHEBI:18135
- ChEMBL:CHEMBL280998
- EPA DTXSID:DTXSID3020257
- PubMed:23122078
- PubMed:23107737
- PubMed:23101658
- PubMed:23084066
- PubMed:23081836
- PubMed:23079526
- PubMed:23071683
- PubMed:23071628
- PubMed:23054709
- PubMed:23035942
- PubMed:23022512
- PubMed:23022412
Advanced structure statistics
- Defined atom stereocentres
- 0
- Undefined atom stereocentres
- 0
- Defined bond stereocentres
- 0
- Undefined bond stereocentres
- 0
- 3D pharmacophore features
- 3
- 3D rings
- 1
- 3D hydrophobes
- 0
- 3D acceptor features
- 0
- 3D donor features
- 2
- 3D anionic centres
- 0
- 3D cationic centres
- 0
- 3D conformers
- 1
- Effective 3D rotors
- 0.0
Machine-readable structure identifiers
- SMILES
C1=CC=C(C(=C1)O)O- InChI
InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H- InChIKey
YCIMNLLNPGFGHC-UHFFFAOYSA-N
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Autoignition Temperature: 510 °C Source: Hazardous Substances Data Bank (HSDB)
- Autoignition Temperature: 510 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 473 °F at 760 mmHg (sublimes) (NTP, 1992) Source: CAMEO Chemicals
- Boiling Point: 245 °C Source: DrugBank
- Boiling Point: 245.5 °C at 760 mm Hg; sublimes Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: BP: 221.5 °C at 400 mm Hg; 197.7 °C at 200 mm Hg; 176 °C at 100 mm Hg; 161.7 °C at 60 mm Hg; 134 °C at 20 mm Hg; 118.3 °C at 10 mm Hg; 104 °C at 5 mm Hg ... Volatile with steam Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 245.5 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 474 °F Source: Occupational Safety and Health Administration (OSHA)
- Boiling Point: 245 °C @760 [mm Hg] Source: PAC Chemical Database, U.S. Department of Energy
- Boiling Point: 474 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Color/Form: Monoclinic tablets, prisms from toluene ... its aqueous solutions soon turn brown Source: Hazardous Substances Data Bank (HSDB)
- Color/Form: Colorless crystals, discolors to brown on exposure to air and light, especially when moist Source: Hazardous Substances Data Bank (HSDB)
- Density: 1.344 at 68 °F (USCG, 1999) - Denser than water; will sink Source: CAMEO Chemicals
- Density: 1.344 Source: Hazardous Substances Data Bank (HSDB)
- Density: Density: 1.371 Source: Hazardous Substances Data Bank (HSDB)
- Density: Relative density (water = 1): 1.3 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Density: 1.34 Source: Occupational Safety and Health Administration (OSHA)
- Density: 1.344 @ 20°C Source: PAC Chemical Database, U.S. Department of Energy
- Density: 1.34 Source: The National Institute for Occupational Safety and Health (NIOSH)
- pKa: 9.45 (at 25 °C) Source: DrugBank
- Dissociation Constants: pKa1 = 9.45; pKa2 = 12.8 Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 261 °F (NTP, 1992) Source: CAMEO Chemicals
- Flash Point: 127 °C Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Flash Point: 260 °F (127 °C) (Closed cup) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 127.2 °C (open cup) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 127 °C (261 °F) (Closed cup) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 127 °C c.c. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Flash Point: 261 °F Source: Occupational Safety and Health Administration (OSHA)
- Flash Point: 261 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- LogP: 0.88 Source: DrugBank
- LogP: log Kow = 0.88 Source: Hazardous Substances Data Bank (HSDB)
- LogP: 0.88 Source: Human Metabolome Database (HMDB)
- LogP: 0.88 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: 221 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: 105 °C Source: DrugBank
- Melting Point: 105 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: 105 °C Source: Human Metabolome Database (HMDB)
- Melting Point: 105 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: 221 °F Source: Occupational Safety and Health Administration (OSHA)
- Melting Point: 104.6 °C Source: PAC Chemical Database, U.S. Department of Energy
- Melting Point: 221 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Odor: Faint characteristic odor Source: Hazardous Substances Data Bank (HSDB)
- Odor: Phenolic odor Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: Solid; white; odorless. Sinks and mixes with water. (USCG, 1999) Source: CAMEO Chemicals
- Physical Description: Large Crystals; Other Solid Source: EPA Chemical Data Reporting (CDR)
- Physical Description: Colorless, crystalline solid with a faint odor; Note: Discolors to brown in air & light; [NIOSH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: Solid Source: Human Metabolome Database (HMDB)
- Physical Description: COLOURLESS CRYSTALS WITH CHARACTERISTIC ODOUR. TURNS BROWN ON EXPOSURE TO AIR AND LIGHT. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Physical Description: Colorless, crystalline solid with a faint odor. Source: Occupational Safety and Health Administration (OSHA)
- Physical Description: Colorless, crystalline solid with a faint odor. [Note: Discolors to brown in air & light.] Source: The National Institute for Occupational Safety and Health (NIOSH)
- Refractive Index: Index of refraction: 1.604 at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: greater than or equal to 100 mg/mL at 70.7 °F (NTP, 1992) Source: CAMEO Chemicals
- Solubility: 461000 mg/L (at 25 °C) Source: DrugBank
- Solubility: In water, 4.61X10+5 mg/L at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Soluble in chloroform, ether; very soluble in pyridine, aqueous alkalis Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Very soluble in alcohol, ethyl ether, acetate Source: Hazardous Substances Data Bank (HSDB)
- Solubility: 461.0 mg/mL Source: Human Metabolome Database (HMDB)
- Solubility: Solubility in water, g/100ml at 20 °C: 43 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Solubility: 44% Source: The National Institute for Occupational Safety and Health (NIOSH)
- Vapor Pressure: 5 mmHg at 219 °F ; 10 mmHg at 244.9 °F (NTP, 1992) Source: CAMEO Chemicals
- Vapor Pressure: 0.03 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: VP: 10 mm Hg at 118.3 °C Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: 3X10-2 mm Hg at 20 °C (extrapolated) Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: Vapor pressure, Pa at 20 °C: 3 (negligible) Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Vapor Pressure: 10 mmHg at 245 °F Source: Occupational Safety and Health Administration (OSHA)
- Vapor Pressure: (244 °F): 10 mmHg Source: The National Institute for Occupational Safety and Health (NIOSH)
- IARC Carcinogenic Agent: Catechol Source: International Agency for Research on Cancer (IARC)
- IARC Carcinogenic Classes: Group 2B: Possibly carcinogenic to humans Source: International Agency for Research on Cancer (IARC)
- IARC Monographs: Volume 15: (1977) Some Fumigants, the Herbicides 2,4-D and 2,4,5-T, Chlorinated Dibenzodioxins and Miscellaneous Industrial Chemicals; Volume Sup 7: Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42, 1987; 440 pages; ISBN 92-832-1411-0 (out of print); Volume 71: (1999) Re-evaluation of Some Organic Chemicals, Hydrazine and Hydrogen Peroxide (Part 1, Part 2, Part 3) Source: International Agency for Research on Cancer (IARC)
- Publication Year: 1999 Source: International Agency for Research on Cancer (IARC)
- Evaluation Year: 1998 Source: International Agency for Research on Cancer (IARC)
- Carcinogen Classification: 2B, possibly carcinogenic to humans. (L135) Source: Toxin and Toxin Target Database (T3DB)
- Exposure Routes: The substance can be absorbed into the body by inhalation of its aerosol, through the skin and by ingestion. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Exposure Routes: inhalation, skin absorption, ingestion, skin and/or eye contact Source: The National Institute for Occupational Safety and Health (NIOSH)
- First Aid: EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.; SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. IMMEDIATELY call a hospital or poison control center even if no symptoms (such as redness or irritation) develop. IMMEDIATELY transport the victim to a hospital for treatment after washing the affected areas.; INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whene Source: CAMEO Chemicals
- First Aid: (General first aid procedures); Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.; Skin: Water wash immediately - If this chemical contacts the skin, immediately wash the contaminated skin with water. If this chemical penetrates the clothing, immediately remove the clothing and wash the skin with water. If symptoms occur after washing, get medical attention immediately.; Breathing: Respiratory support; Swallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately. Source: The National Institute for Occupational Safety and Health (NIOSH)
- Signal: Danger Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- GHS Hazard Statements: H301: Toxic if swallowed [Danger Acute toxicity, oral]; H311: Toxic in contact with skin [Danger Acute toxicity, dermal]; H315: Causes skin irritation [Warning Skin corrosion/irritation]; H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H341: Suspected of causing genetic defects [Warning Germ cell mutagenicity]; H350: May cause cancer [Danger Carcinogenicity] Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Precautionary Statement Codes: P203, P262, P264, P264+P265, P270, P280, P301+P316, P302+P352, P305+P351+P338, P316, P318, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P405, and P501 (click each P-code to see the statement) Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Signal: Danger Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H301 (16.4%): Toxic if swallowed [Danger Acute toxicity, oral]; H302 (83.6%): Harmful if swallowed [Warning Acute toxicity, oral]; H311 (16.4%): Toxic in contact with skin [Danger Acute toxicity, dermal]; H312 (83.6%): Harmful in contact with skin [Warning Acute toxicity, dermal]; H315 (> 99.9%): Causes skin irritation [Warning Skin corrosion/irritation]; H317 (12.6%): May cause an allergic skin reaction [Warning Sensitization, Skin]; H319 (94.6%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H341 (16.4%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]; H350 (11.4%): May cause cancer [Danger Carcinogenicity] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P203, P261, P262, P264, P264+P265, P270, P272, P280, P301+P316, P301+P317, P302+P352, P305+P351+P338, P316, P317, P318, P321, P330, P332+P317, P333+P317, P337+P317, P361+P364, P362+P364, P405, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
- ECHA C&L Notifications Summary: Aggregated GHS information provided per 2962 reports by companies from 34 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
- Signal: Warning Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]; H412 (100%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P261, P272, P273, P280, P302+P352, P321, P333+P317, P362+P364, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
- ECHA C&L Notifications Summary: The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]; H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H412 (100%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: European Chemicals Agency (ECHA)
- NFPA Health Rating: 3 - Materials that, under emergency conditions, can cause serious or permanent injury. Source: Hazardous Substances Data Bank (HSDB)
- NFPA Fire Rating: 1 - Materials that must be preheated before ignition can occur. Materials require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur. Source: Hazardous Substances Data Bank (HSDB)
- NFPA Instability Rating: 0 - Materials that in themselves are normally stable, even under fire conditions. Source: Hazardous Substances Data Bank (HSDB)
- Target Organs: Eyes, skin, respiratory system, central nervous system, kidneys Source: The National Institute for Occupational Safety and Health (NIOSH)
- Cosmetic Ingredient Review Conclusion: The CIR Expert Panel concludes that Pyrocatechol is unsafe for use in leave-on products, and that the available data are insufficient to support the safety of Pyrocatechol as used in hair dyes. Source: Cosmetic Ingredient Review (CIR)
- Cosmetic Ingredient Review Finding(s): The ingredient is unsafe for use in cosmetics; Ingredients for which the data are insufficient and their use in cosmetics is not supported Source: Cosmetic Ingredient Review (CIR)
- Toxicity Summary: IDENTIFICATION AND USE: Catechol is a tablet or colorless crystal, prism or aqueous solution, which discolors to brown on exposure to air and light. It has a faint characteristic odor. It is used as antioxidant in the rubber, chemical, photographic, dye, fat, and oil industries. It was formerly used as an antiseptic. Catechol was found unsafe for use in cosmetics. HUMAN EXPOSURE AND TOXICITY: Catechol contact with the skin has been known to cause an eczematous dermatitis. It is highly irritating upon direct contact; severe eye and deep skin burns result. Well absorbed by skin. Systemic toxicity similar to that of phenol however, catechol may be more likely to cause convulsions and hypertension. At high doses, renal and liver injury may occur. Absorption through the skin, in a few instances, has resulted in symptoms of illness resembling closely those induced by phenol, except for certain central effects (convulsions) that were more marked. Death apparently is initiated by respiratory failure. Catechol was found to be a more harmful toxin than phenol in human blood cells in vitro, since it provokes statistically significant changes in the function of erythrocytes even at low doses. Source: Hazardous Substances Data Bank (HSDB)
- Environmental Bioconcentration: An estimated BCF of 3 was calculated for catechol(SRC), using a log Kow of 0.88(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: TERRESTRIAL FATE: Based on a classification scheme(1), a Koc value of 118(2), indicates that catechol is expected to have high mobility in soil(SRC). Volatilization of catechol from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.2X10-9 atm-cu m/mole(SRC), based upon its vapor pressure, 3.66X10-3 mm Hg(3), and water solubility, 4.61X10+5 mg/L(4). Catechol is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). The percent biodegradation after 6 months in various loam soils ranged from 24 to 50%(5), indicating that biodegradation is a moderate environmental fate process in soil(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a classification scheme(1), a Koc value of 118(2), indicates that catechol is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 1.20X10-9 atm-cu m/mole(SRC), derived from its vapor pressure, 3.66X10-3 mm Hg(4), and water solubility, 4.61X10+5 mg/L(5). According to a classification scheme(6), an estimated BCF of 3(SRC), from its log Kow of 0.88(7) and a regression-derived equation(8), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Utilizing the Japanese MITI test, 83% of the Theoretical BOD was reached in 2 weeks(9) indicating that biodegradation is an important environmental fate process in water(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), catechol, which has a vapor pressure of 3.66X10-3 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase catechol is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 2.8 hrs(SRC), calculated from its rate constant of 1.04X10-10 cu cm/molecule-sec at 25 °C(3). Catechol in its nonionized form will not be subject to direct photolysis since this form does not absorb light above 300 nm in methanol solution(4). Reaction of catechol with nitrate radicals during nighttime may be an important removal process based on a rate constant of 3.8X10-12 cu cm/molecule sec for the reaction of phenol with nitrate radicals(2) which corresponds to a half-life of 15 minutes at an atmospheric concentration of 2X10+8 nitrate radicals per cu cm(SRC). The ionized form of catechol may photolyze based on an absorption maximum at 313 nm in basic aqueous solution(6) and at 289 nm in basic methanol solution(4). Therefore, catechol may be susceptible Source: Hazardous Substances Data Bank (HSDB)
- Consumer Uses: Intermediate Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Intermediate Source: EPA Chemical Data Reporting (CDR)
- Cosmetic Ingredient Review Link: CIR ingredient: Pyrocatechol Source: Cosmetic Ingredient Review (CIR)
- Uses: Catechol is used as a photographic developer, a developer for fur dyes, as an intermediate for antioxidants in rubber and lubricating oils, in polymerization inhibitors, and in pharmaceuticals. Source: EPA Hazardous Air Pollutants
- Sources/Uses: Used in the photography, rubber, dye, and oil industries as an antioxidant; also used to produce cosmetics and pharmaceuticals; [ACGIH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Industrial Processes with risk of exposure: Photographic Processing [Category: Other] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Activities with risk of exposure: Smoking cigarettes [Category: Food & Drugs] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: Antiseptic /former US/, photography, dyestuffs, electroplating, specialty inks, antioxidants and light stabilizers, organic synthesis. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Antioxidant in the rubber, chemical, photographic, dye, fat, and oil industries. It is also employed in cosmetics as couplers in oxidative hair dyes, but is no longer used as an antiseptic. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Synthesis of food, pharmaceutical and agricultural products Source: Hazardous Substances Data Bank (HSDB)
- Uses: The Cosmetic Ingredient Review Panel concludes that pyrocatechol is unsafe for use in leave-on products and that the available data are insufficient to support the safety of pyrocatechol as used in hair dyes. This conclusion supersedes the earlier conclusion issued by the Expert Panel in 1985. Source: Hazardous Substances Data Bank (HSDB)
- Uses: For more Uses (Complete) data for CATECHOL (7 total), please visit the HSDB record page. Source: Hazardous Substances Data Bank (HSDB)
- Uses: This is a man-made compound that is used as a pesticide. Source: Toxin and Toxin Target Database (T3DB)
Mapped by: Existing checksum-valid CAS to unique PubChem CID match. Retrieved: 2026-08-31. Open source record
Scientific classifications and hazard annotations provide context and do not replace the market-specific regulatory decision shown above.
Additional source coverage and match status
| Source | Result | Checked |
|---|---|---|
| NIH PubChem PUG-View | Exact match | 2026-08-31 |
A recorded no-match is useful evidence that the source was checked; it is not a claim that the substance does not exist elsewhere.
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Official source and provenance
- Registered source
- Great Britain Cosmetics Regulation — consolidated Annexes II–VI and amendments
- Source reference
- GB Cosmetics Regulation, Annex II, entry 408
- Source record ID
II-408- Source version
- 2026-08-15
- Source language
- English
- Translation status
- Original is English
- Effective date
- 2026-08-15
- Source updated
- 2026-08-19
- Snapshot checked
- 2026-08-30 04:51 UTC
- Validation method
- legislation.gov.uk XML table parse; {'II': 1758, 'III': 326, 'IV': 154, 'V': 57, 'VI': 34}
- SHA-256
e3a386d950f54c6e7a7f9e784d1bd46e52de725137e89d5630709824475215d8
Registered dataset notes
- Dataset coverage
- Complete consolidated GB Annexes II–VI, with later amendments versioned separately
- Authority note
- Binding GB schedules and versioned amendments to retained Regulation 1223/2009; applies to England, Wales and Scotland, not Northern Ireland
- Source licence
- Open Government Licence v3.0 / Crown copyright
- Attribution
- Contains public sector information licensed under the Open Government Licence v3.0.
How this record fits the market dataset
Status distribution
Condition text is present on 517 of 2329 current records. An empty condition field is interpreted according to the record type above; it is never converted into an unrestricted-use claim.
Great Britain market context
Complete consolidated annex dataset
Coverage version: GB retained Regulation 1223/2009 schedules, effective 15 August 2026
Current consolidated Annexes II–VI for England, Scotland and Wales.
Verification checklist
- Confirm INCI/CAS/EC identity.
- Review every current GB Annex II–VI match.
- Check commencement dates and later statutory instruments.
- Verify SCPN, responsible-person, safety-report and labelling duties.
Official market sources
- Great Britain Cosmetics Regulation — consolidated Annexes II–VI and amendmentsBinding GB schedules and versioned amendments to retained Regulation 1223/2009; applies to England, Wales and Scotland, not Northern Ireland
Verification workflow and record completeness
Before using this result in a compliance decision
- Confirm that “Pyrocatechol (Catechol)” and every CAS/EC identifier refer to the material in your supplier specification.
- Confirm INCI/CAS/EC identity.
- Review every current GB Annex II–VI match.
- Check commencement dates and later statutory instruments.
- Verify SCPN, responsible-person, safety-report and labelling duties.
- Document the source version and recheck the regulator before manufacture, notification or market placement.
Fields available in this record
- Official substance nameAvailable
- CASAvailable
- ECAvailable
- Separate condition textNot present in source row
- Effective dateAvailable
- Snapshot hash and methodAvailable
Questions this page answers
Stable citation
Pyrocatechol (Catechol). GB Cosmetics Regulation, Annex II, entry 408. Great Britain. Source version 2026-08-15. CosIng Checker regulatory record: https://cosingchecker.com/regulations/gb/records/4763/
Cite the regulator as the legal authority. This page is a structured evidence index and verification aid, not a substitute for the official text or professional legal assessment.
Interpretation and limits for Great Britain
This official record identifies the substance as prohibited for cosmetic use in the stated market scope.
Do not rely on a formulation containing this identity until the cited source, effective date and exact substance match have been verified.
How to interpret the legal role
The cited row forms part of a binding rule or legally incorporated list for this market.
Evidence on this page
- Recorded outcome: Prohibited
- Legal role: Binding rule
- Source version: 2026-08-15
- Effective date: 2026-08-15
What it does not prove
No annex match is not approval and does not cover Northern Ireland, which follows the applicable EU framework.
Further authoritative substance research
These sources can add identity, safety, exposure or hazard context. A link is not evidence that the database contains this exact substance, and none of these sources overrides the market decision above.
Cosmetic Ingredient Review safety assessments
Expert Panel conclusions, assessed ingredient groups, use conditions, dates and report documents
Independent expert review considered by FDA; not a government approval or binding market rule
Research this identity at the sourceFDA Global Substance Registration System
UNII identifiers, preferred names, substance types, codes and public substance relationships
Identity registry only; UNII availability does not imply FDA review or approval
Research this identity at the sourceILO/WHO International Chemical Safety Cards
Hazards, symptoms, first aid, storage, incompatibilities and physical properties for covered chemicals
International occupational chemical-safety reference; not cosmetic-use approval
Research this identity at the sourceJapan NITE-CHRIP
Chemical identity, Japanese and foreign legal lists, GHS hazards and exposure-related information
Chemical-management evidence; cosmetic status remains governed by the applicable MHLW standard and market rules
Research this identity at the sourceNIOSH Pocket Guide to Chemical Hazards
REL, PEL, IDLH, properties, exposure routes, symptoms, target organs, first aid and measurement methods for covered workplace chemicals
US occupational-health guidance and limits; not a cosmetic ingredient decision
Research this identity at the sourceOECD eChemPortal
Gateway to authority-owned physical-property, fate, ecotoxicity, toxicity, exposure and GHS records
Discovery gateway; each linked authority remains responsible for its data
Research this identity at the sourceUS EPA CompTox CTX APIs
API key required for importDTXSID identity, experimental and predicted properties, toxicity, bioactivity, exposure and environmental data
Scientific and computational evidence; predictions must remain labelled and do not determine cosmetic legality
Research this identity at the source