INDOLE
Indole
INDOLE is listed in the EU CosIng inventory, but no direct annex records are linked on this page yet.
Regulatory evidence by market
No rule for this ingredient has been imported for any of the 13 markets tracked here.
That describes this inventory, not the law. No imported rule is not evidence that an ingredient is permitted: a rule may exist under another name or identifier, or in a dataset not yet imported here.
Chemical identity and properties

Indole
1H-indole is an indole and a polycyclic heteroarene. It has a role as an Escherichia coli metabolite. It is a tautomer of a 3H-indole. — ChEBI
- IUPAC name
- 1H-indole
- Molecular formula
- C8H7N
- Molecular weight
- 117.15 g/mol
- Exact mass
- 117.057849228 Da
- XLogP3
- 2.1
- Topological polar surface area
- 15.8 Ų
- Hydrogen-bond donors
- 1
- Hydrogen-bond acceptors
- 0
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:16881
- ChEMBL:CHEMBL15844
- EPA DTXSID:DTXSID0020737
- PubMed:23449869
- PubMed:23125706
- PubMed:23122407
- PubMed:23114508
- PubMed:23109863
- PubMed:23106081
- PubMed:23094066
- PubMed:23090023
- PubMed:23079493
- PubMed:23074901
- PubMed:23072812
- PubMed:23065612
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Boiling Point: 254 °C Source: DrugBank
- Boiling Point: 253 °C @ 762 mm Hg; 128-133 °C @ 28 mm Hg Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 253.00 to 254.00 °C. @ 760.00 mm Hg Source: Human Metabolome Database (HMDB)
- Color/Form: LEAFLETS (WATER, PETROLEUM), CRYSTALS (ETHER) Source: Hazardous Substances Data Bank (HSDB)
- Color/Form: Colorless to yellowish scales, turning red on exposure to light and air. Source: Hazardous Substances Data Bank (HSDB)
- Color/Form: WHITE CRYSTALLINE SOLID Source: Hazardous Substances Data Bank (HSDB)
- Color/Form: Colorless, shiny flakes Source: Hazardous Substances Data Bank (HSDB)
- Density: 1.22 g/cu cm at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Dissociation Constants: pKa (basic)= -2.4 Source: Hazardous Substances Data Bank (HSDB)
- LogP: 2.14 Source: DrugBank
- LogP: Log P= 2.14 Source: Hazardous Substances Data Bank (HSDB)
- LogP: 2.14 Source: Human Metabolome Database (HMDB)
- Melting Point: 52.5 °C Source: DrugBank
- Melting Point: 52 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: Heat of Formation= 1.5660X10+8 J/kmol; Heat of Fusion at the Melting Point= 9.0000X10+6 J/kmol Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: 52.5 °C Source: Human Metabolome Database (HMDB)
- Odor: ALMOST FLORAL ODOR WHEN HIGHLY PURIFIED, OTHERWISE EXHIBITS CHARACTERISTIC ODOR OF FECES Source: Hazardous Substances Data Bank (HSDB)
- Odor: Unpleasant odor in high concentration but pleasant in dilute solution. Source: Hazardous Substances Data Bank (HSDB)
- Odor: Light jasmine odor Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: Dry Powder; Liquid Source: EPA Chemical Data Reporting (CDR)
- Physical Description: White to yellowish solid with an unpleasant odor; Pleasant odor in dilute solutions; Turns red when exposed to light or air; [Hawley] White or yellow crystalline powder; [MSDSonline] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: Solid Source: Human Metabolome Database (HMDB)
- Physical Description: White lustrous, flakey crystalline solid; Unpleasant odour at high concentration, odour becomes floral at higher dilutions Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Solubility: 3560 mg/L (at 25 °C) Source: DrugBank
- Solubility: SOL IN HOT WATER, HOT ALC, ETHER, BENZENE Source: Hazardous Substances Data Bank (HSDB)
- Solubility: 1 G IN 2 ML OF 70% ALC Source: Hazardous Substances Data Bank (HSDB)
- Solubility: SOL IN TOLUENE Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Soluble in fixed oils; insoluble in mineral oil and glycerol. Source: Hazardous Substances Data Bank (HSDB)
- Solubility: For more Solubility (Complete) data for INDOLE (6 total), please visit the HSDB record page. Source: Hazardous Substances Data Bank (HSDB)
- Solubility: 3.56 mg/mL Source: Human Metabolome Database (HMDB)
- Solubility: Soluble in fixed oils and propylene glycol; Insoluble in glycerol Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Solubility: Soluble (in ethanol) Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Vapor Pressure: 0.01 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: 0.0122 mm Hg at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Signal: Danger Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]; H311 (99%): Toxic in contact with skin [Danger Acute toxicity, dermal]; H318 (11.6%): Causes serious eye damage [Danger Serious eye damage/eye irritation] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P262, P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P354+P338, P316, P317, P321, P330, P361+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 1996 reports by companies from 22 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: Danger Source: NITE-CMC
- GHS Hazard Statements: H302: Harmful if swallowed [Warning Acute toxicity, oral]; H311: Toxic in contact with skin [Danger Acute toxicity, dermal]; H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation] Source: NITE-CMC
- Precautionary Statement Codes: P262, P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P351+P338, P316, P321, P330, P337+P317, P361+P364, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- Environmental Bioconcentration: An estimated BCF value of 25 was calculated for indole(SRC), using a measured log Kow of 2.14(1) and a recommended regression-derived equation(2). According to a classification scheme(3), this BCF value suggests that bioconcentration in aquatic organisms is low(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: TERRESTRIAL FATE: Based on a recommended classification scheme(1), an estimated Koc value of 350(SRC), determined from a measured log Kow(2) and a recommended regression-derived equation(3), and a measured Koc of 187 from a synthetic soil with 0-2% added humic acid(4), indicate that indole will have moderate mobility in soil(SRC). Volatilization of indole should not be important from moist soil surfaces(SRC) given an estimated Henry's Law constant of 5.3X10-7 atm-cu m/mole(SRC), calculated from experimental values for vapor pressure(5) and water solubility(6). Indole is expected to readily biodegrade under both aerobic and anaerobic conditions in soil(SRC). Indole, added to Chernozem soil at 1 and 10 g/kg soil, was completely biodegraded in 19 and 135 days, respectively(7). Indole was completely biodegraded by suspensions of an organic soil (Carlisle muck) under methanogenic and denitrifying conditions within 67 and 144 days, respectively; oxindole was reported as a metabolite of this process(8). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a recommended classification scheme(1), an estimated Koc value of 350(SRC), determined from a measured log Kow(2) and a recommended regression-derived equation(1), and a measured Koc value of 187(3) indicate that indole may adsorb to suspended solids and sediment in water(SRC). Indole is not expected to volatilize from water surfaces(1,SRC) based on an estimated Henry's Law constant of 5.3X10-7 atm-cu m/mole(SRC), calculated from experimental values for vapor pressure(4) and water solubility(5). According to a classification scheme(6), an estimated BCF value of 25(1,SRC), from a measured log Kow(2), suggests that bioconcentration in aquatic organisms is low(SRC). Indole is expected to readily biodegrade under both aerobic and anaerobic conditions in water(SRC). At 10 °C, aerobic groundwater containing a mixture of aromatic compounds completely biodegraded indole in 310 hours, including an acclimation period of 130 hours(7). Complete metabolism of indole by methanogenic sediments from the shore, edge, and bottom of Buffalo Run stream, PA, occurred within 33 days; oxindole was formed during this process(8). Indole was completely biodegraded under denitrifying c 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), indole, which has a measured vapor pressure of 0.0122 mm Hg at 25 °C(2), will exist solely as a vapor in the ambient atmosphere. Vapor-phase indole is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals, nitrate radicals, and ozone(SRC); the half-lives for these reactions in air are estimated to be about 2 to 3 hours, < 1 minute, and 6 hours, respectively(3,SRC). Source: Hazardous Substances Data Bank (HSDB)
- Consumer Uses: Fragrance Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Laboratory chemicals Source: EPA Chemical Data Reporting (CDR)
- Sources/Uses: Found in feces, neroli oil, jasmine oil, orange-blossom oil, certain flowers, tobacco smoke, and coal tar; Used in perfumery, flavoring, and as chemical reagent, intermediate, and feedstock; [HSDB] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: USED IN PERFUMERY Source: Hazardous Substances Data Bank (HSDB)
- Uses: SYNTHETIC FLAVOR Source: Hazardous Substances Data Bank (HSDB)
- Uses: Chemical reagent Source: Hazardous Substances Data Bank (HSDB)
- Uses: Used as a chemical intermediate for the synthesis of indol-3-ylacetic acid; 4-indol-3-ylbutyric acid; L-tryptophan. Source: Hazardous Substances Data Bank (HSDB)
- Uses: For more Uses (Complete) data for INDOLE (6 total), please visit the HSDB record page. Source: Hazardous Substances Data Bank (HSDB)
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.
Inventory details for INDOLE
INCI name
INDOLE
Description
Indole
Record provenance
- Inventory reference
- 40299
- Imported identity
- INDOLE
- Source update
- 02/03/2011
Annex records for INDOLE
Key data
Related inventory evidence
Ingredients with overlapping formulation functions
Additional official and scientific sources
11 external databases to check this identity in
Each link searches that source for this identity. What each source is, and its legal weight
How INDOLE appears in the CosIng inventory
The CosIng inventory lists INDOLE as a cosmetic ingredient and this page links it to 0 annex records. The inventory entry captures names and identifiers, while the annex records show where the substance is prohibited, restricted or positively listed in EU cosmetics law.
INDOLE is also tagged with 1 cosmetic function in the official data. Function labels describe intended use, but they do not replace regulatory review of linked annex records before formulation or labelling work.
Frequently asked questions
Source note for INDOLE
This page reproduces the CosIng inventory entry for INDOLE from public European Commission cosmetic ingredient materials and shows linked identifiers even when no direct annex match is currently attached.
Use this inventory page to research INDOLE and compare linked records, but verify restrictions and legal status against the current official source text and law before making regulatory decisions.
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