InventoryRef 7430215/10/2010
ANETHOLE
Benzene, 1-methoxy-4-(1-propenyl)-
ANETHOLE is linked to 1 EU annex record on this page.
Regulatory evidence by market
This matrix separates verified ingredient rules from sources that are mapped but not yet imported. No imported rule does not mean the ingredient is permitted.
Swipe or scroll horizontally to see every column.
| Market | Evidence status | Records | Source language |
|---|---|---|---|
| European Union | Evidence linked Restricted entry found Open this evidence | 1 | English and EU languages |
| Great Britain | Source mapped Official source mapped; ingredient rule not imported | 0 | English |
| Canada | Source mapped Official source mapped; ingredient rule not imported | 0 | English and French |
| New Zealand | Source mapped Official source mapped; ingredient rule not imported | 0 | English |
| ASEAN | Source mapped Official source mapped; ingredient rule not imported | 0 | English and national languages |
| China | Source mapped Official source mapped; ingredient rule not imported | 0 | Chinese with selected English material |
| Japan | Source mapped Official source mapped; ingredient rule not imported | 0 | Japanese; official English translation available |
| South Korea | Source mapped Official source mapped; ingredient rule not imported | 0 | Korean with some English names |
| United States | Source mapped Official source mapped; ingredient rule not imported | 0 | English |
| Australia | Source mapped Official source mapped; ingredient rule not imported | 0 | English |
| Brazil | Source mapped Official source mapped; ingredient rule not imported | 0 | Portuguese with INCI crosswalks |
| India | Source mapped Official source mapped; ingredient rule not imported | 0 | English and Hindi |
| Saudi Arabia | Evidence linked Restricted Open this evidence | 1 | Arabic and English |
Chemical identity and properties
CAS 104-46-1PubChem CID 637563
Anethole
Anethole is a monomethoxybenzene that is methoxybenzene substituted by a prop-1-en-1-yl group at position 4. It has a role as a plant metabolite. — ChEBI
- IUPAC name
- 1-methoxy-4-[(E)-prop-1-enyl]benzene
- Molecular formula
- C10H12O
- Molecular weight
- 148.20 g/mol
- Exact mass
- 148.088815002 Da
- XLogP3
- 3.3
- Topological polar surface area
- 9.2 Ų
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 1
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
Anise camphorMonasirupAnethol4-PropenylanisoleAnisole, p-propenyl-trans-p-Propenylanisolep-Anethole1-Methoxy-4-(1-propenyl)benzene
16 more reported names
Aniskampfertrans-1-p-AnisylpropeneAnethole, transp-1-Propenylanisole1-Methoxy-4-propenylbenzene4-MethoxypropenylbenzeneBenzene, 1-methoxy-4-(1-propenyl)-p-Propenylphenyl methyl etherFEMA No. 20864-Methoxy-1-propenylbenzeneAcintene OPropene, 1-(p-methoxyphenyl)-1-Propene, 1-(4-methoxyphenyl)-FEMA Number 2086Q3JEK5DO4Kp-Methoxy-beta-methylstyrene
External database identifiers
- ChEBI:CHEBI:2716
- ChEBI:CHEBI:35616
- ChEMBL:CHEMBL452630
- EPA DTXSID:DTXSID9020087
- PubMed:40796067
- PubMed:39029857
- PubMed:37987213
- PubMed:35430261
- PubMed:29191726
- PubMed:27420082
- PubMed:26795242
- PubMed:22317828
- PubMed:21212515
- PubMed:20171274
- PubMed:17709257
- PubMed:16573833
Evidence from additional scientific databases
NIH PubChem PUG-View
Exact identifier match637563
Attributed physical-property, hazard, environmental and use annotations.
- Boiling Point: 454.1 °F at 760 mmHg (NTP, 1992) Source: CAMEO Chemicals
- Boiling Point: 234 °C Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 234-239.5 °C Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Color/Form: White crystals Source: Hazardous Substances Data Bank (HSDB)
- Density: 0.9882 (NTP, 1992) - Less dense than water; will float Source: CAMEO Chemicals
- Density: 0.9878 @ 20 °C/4 °C Source: Hazardous Substances Data Bank (HSDB)
- Density: 0.983-0.988 Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Flash Point: 195 °F (NTP, 1992) Source: CAMEO Chemicals
- Flash Point: 90.1 °C Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Melting Point: 70.4 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: 21.3 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: Liquid Molar Volume = 0.1507 cu m/kmol; Heat of Fusion @ Melting Point = 1.60E+7 J/kmol Source: Hazardous Substances Data Bank (HSDB)
- Odor: ANISE OIL ODOR Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: Anethole appears as white crystals or a liquid. Odor of anise oil and a sweet taste. (NTP, 1992) Source: CAMEO Chemicals
- Physical Description: Liquid Source: EPA Chemical Data Reporting (CDR)
- Physical Description: Liquid; CBI Source: EPA Chemical Data Reporting (CDR)
- Physical Description: White solid with an odor of anise; Affected by light; [Hawley] Colorless liquid with a sweet odor of aniseed; [Merck Index] Colorless crystalline solid or liquid; mp = 20-23 deg C; [MSDSonline] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: Colourless to faintly yellow liquid with an aniseed-like odour Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Refractive Index: 1.559-1.562 Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Solubility: Slightly soluble (NTP, 1992) Source: CAMEO Chemicals
- Solubility: 1:8 IN 80% ALCOHOL; 1:1 IN 90% ETHANOL Source: Hazardous Substances Data Bank (HSDB)
- Solubility: ALMOST WATER INSOL; MISCIBLE WITH CHLOROFORM & ETHER Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Water solubility = 1.110E-1 g/l @ 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Slightly soluble in water; miscible with chloroform and ether Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Solubility: 1 ml in 2 ml 96% alcohol (in ethanol) Source: Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Vapor Pressure: 0.05 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: 5.45 Pa @ 294 deg K Source: Hazardous Substances Data Bank (HSDB)
- Viscosity: 2.45X10-3 Pa.s Source: Hazardous Substances Data Bank (HSDB)
- 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. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.; 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. Whenever possible, Self-Contained Breathing Apparatus (SCBA) shou Source: CAMEO Chemicals
- Note: This chemical does not meet GHS hazard criteria for 2.9% (55 of 1880) of reports. Source: European Chemicals Agency (ECHA)
- Signal: Warning Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H317 (95.3%): May cause an allergic skin reaction [Warning Sensitization, Skin] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P261, P272, 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: Aggregated GHS information provided per 1880 reports by companies from 19 notifications to the ECHA C&L Inventory.; Reported as not meeting GHS hazard criteria per 55 of 1880 reports by companies.; There are 18 notifications provided by 1825 of 1880 reports by companies with hazard statement code(s).; 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)
- Note: This chemical does not meet GHS hazard criteria for 6.2% (20 of 321) of reports. Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H317 (93.8%): May cause an allergic skin reaction [Warning Sensitization, Skin]; H412 (36.4%): 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: Aggregated GHS information provided per 321 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Reported as not meeting GHS hazard criteria per 20 of 321 reports by companies.; There are 4 notifications provided by 301 of 321 reports by companies with hazard statement code(s).; 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: Hazardous Chemical Information System (HCIS), Safe Work Australia
- GHS Hazard Statements: H317: May cause an allergic skin reaction [Warning Sensitization, Skin] Source: Hazardous Chemical Information System (HCIS), Safe Work Australia
- Precautionary Statement Codes: P261, P272, P280, P302+P352, P321, P333+P317, P362+P364, and P501 (click each P-code to see the statement) Source: Hazardous Chemical Information System (HCIS), Safe Work Australia
- Environmental Bioconcentration: Based upon an experimental water solubility of 111 mg/l(1), the BCF of anethole can be estimated to be approximately 43.4 from a regression-derived equation(2). This estimated BCF value suggests that bioconcentration in aquatic organisms is not expected to be an important fate process(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: TERRESTRIAL FATE: Anethole will have a medium to low mobility(3) in soil based on estimated Koc values ranging from 327 to 680(1,2). Insufficient data are available to predict the relative importance or rate of biodegradation in soil conditions(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Volatilization of anethole from water is not rapid but could possibly be significant based upon estimated Henry's Law constant of 7.18X10-5 atm cu m/mol(1,2,SRC). Volatilization half-lives from a model river (1 m deep flowing 1 m/sec with a wind velocity of 3 m/sec) and a model lake (1 meter deep) can be estimated to be about 18 hours and 9 days respectively(2). Insufficient data are available to predict the relative importance or rate of biodegradation from natural waters(SRC). Aquatic bioconcentration is not expected to be an important fate process, however, based on a Koc value of 680(3), some absorption to sediment may occur(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: ATMOSPHERIC FATE: Based on an extrapolated vapor pressure of approximately 0.005 mm Hg at 25 °C(1), anethole will exist in the atmosphere in the vapor phase(2). It will degrade in the atmosphere by reaction with photochemically produced hydroxyl radicals with estimated half-lives of 4.9 and 4.5 hrs for the cis and trans isomers, respectively(3). Anethole will also degrade in the atmosphere by reaction with atmospheric ozone with estimated half-lives of 4.03 and 2.02 hrs for the cis and trans isomers, respectively(3). Source: Hazardous Substances Data Bank (HSDB)
- Consumer Uses: Fragrance Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Intermediate Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Other; Intermediates; Fragrance Source: EPA Chemical Data Reporting (CDR)
- Sources/Uses: Chief constituent of anise, star anise, and fennel oils; Used as a flavoring agent (foods, beverages, and drugs) and fragrance (soaps and dentifrices); [Merck Index] Used to make anisaldehyde, as a sensitizer in bleaching colors in photography, an embedding material in microscopy, and an insect attractant; [HSDB] 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
- Uses: The active ingredient is no longer contained in any registered pesticide products ... "cancelled." Source: Hazardous Substances Data Bank (HSDB)
- Uses: MFR ANISALDEHYDE; IN PERFUMERY, SOAP & DENTIFRICES; SENSITIZER IN BLEACHING COLORS IN COLOR PHOTOGRAPHY; AS EMBEDDING MATERIAL IN MICROSCOPY; PHARMACEUTIC AID (FLAVOR); VET: HAS BEEN USED AS A CARMINATIVE & AS A FLAVORING AGENT Source: Hazardous Substances Data Bank (HSDB)
- Uses: AS FLAVOR INGREDIENT Source: Hazardous Substances Data Bank (HSDB)
- Uses: IN LICORICE CANDIES Source: Hazardous Substances Data Bank (HSDB)
- Uses: For more Uses (Complete) data for ANETHOLE (6 total), please visit the HSDB record page. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Use (kg; approx.) in Germany (2009): >25; Consumption (g per capita; approx.) in Germany (2009): 0.000305; Calculated removal (%): 96.6 Source: NORMAN Suspect List Exchange
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 |
|---|---|---|
| EMBL-EBI ChEBI | Needs review | 2026-08-31 |
| 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 2026-09-02 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Inventory details for ANETHOLE
INCI name
ANETHOLE
Description
Benzene, 1-methoxy-4-(1-propenyl)-
Record provenance
- Inventory reference
- 74302
- Imported identity
- ANETHOLE
- Source update
- 15/10/2010
Annex records for ANETHOLE
Key data
CAS
EC
Restriction
—
Function
- DENATURANT
- Rendering cosmetics unpalatable. Mostly added to cosmetics containing ethyl alcohol to make it unsuitable for ingestion.
- FRAGRANCE
- Imparting an odour or taste. Creating a perceivable pleasant smell and/or masking a bad smell.
Official EU ingredient-name evidence
The ingredient name exactly matches the official 2025 EU glossary of common ingredient names.
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
ECHA CHEM / Information on chemicalsPubChem PUG RESTEU Safety Gate cosmetic product alertsECHA CHEMUS EPA CompToxCosmetic Ingredient Review safety assessmentsFDA Global Substance Registration SystemILO/WHO International Chemical Safety CardsJapan NITE-CHRIPNIOSH Pocket Guide to Chemical HazardsOECD eChemPortal
How ANETHOLE appears in the CosIng inventory
The CosIng inventory lists ANETHOLE as a cosmetic ingredient and this page links it to 1 annex record. The inventory entry captures names and identifiers, while the annex record shows where the substance is prohibited, restricted or positively listed in EU cosmetics law.
ANETHOLE is also tagged with 2 cosmetic functions 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
ANETHOLE appears in the EU CosIng inventory and has linked annex records. Check the annex records above for applicable restrictions, concentration limits and conditions of use. Annex II listing means prohibited; Annex III means restricted; Annexes IV, V and VI mean permitted under specified conditions.
According to the EU CosIng inventory, ANETHOLE carries the following function designation(s):
CAS 104-46-1 may appear across multiple EU annex records. Viewing the CAS lookup page shows all Annex II–VI entries sharing this identifier, which is useful for identifying cross-annex regulatory status of the same chemical substance.
Use the INCI Checker to screen a full ingredient list across selected markets, or compare this substance across all supported market datasets.
Source note for ANETHOLE
This page combines the CosIng inventory entry for ANETHOLE with 1 linked Annex II–VI record from the local dataset built from public European Commission cosmetic ingredient materials.
Use this inventory page to research ANETHOLE and compare linked records, but verify restrictions and legal status against the current official source text and law before making regulatory decisions.
Tools & next steps
Check your formula
Scan a full INCI list to detect ANETHOLE and any linked EU annex restrictions or allergen flags.
INCI CheckerSearch similar ingredients
Find other inventory ingredients and annex entries related to ANETHOLE, its identifiers or nearby name variants.
Search