1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether)
1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether) is listed in Annex II as a prohibited substance for cosmetic products placed on the EU market.
Chemical identity and properties

Phenyl glycidyl ether
Phenyl glycidyl ether is a colorless liquid. (NTP, 1992) — CAMEO Chemicals
- IUPAC name
- 2-(phenoxymethyl)oxirane
- Molecular formula
- C9H10O2
- Molecular weight
- 150.17 g/mol
- Exact mass
- 150.068079557 Da
- XLogP3
- 1.6
- Topological polar surface area
- 21.8 Ų
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 2
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:82367
- ChEMBL:CHEMBL1568222
- EPA DTXSID:DTXSID8021145
- PubMed:22346986
- PubMed:22290177
- PubMed:22196513
- PubMed:22012271
- PubMed:21765830
- PubMed:21751775
- PubMed:21731544
- PubMed:21567703
- PubMed:21370839
- PubMed:21361271
- PubMed:21054058
- PubMed:20471590
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Boiling Point: 473 °F at 760 mmHg (NTP, 1992) Source: CAMEO Chemicals
- Boiling Point: 245 °C Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 245 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 473 °F Source: Occupational Safety and Health Administration (OSHA)
- Boiling Point: 473 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Color/Form: Colorless liquid (Note: A solid below 38 degrees F) Source: Hazardous Substances Data Bank (HSDB)
- Density: 1.1092 at 68 °F (NTP, 1992) - Denser than water; will sink Source: CAMEO Chemicals
- Density: 1.1109 at 21 °C Source: Hazardous Substances Data Bank (HSDB)
- Density: Relative density (water = 1): 1.11 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Density: 1.11 Source: Occupational Safety and Health Administration (OSHA)
- Density: 1.11 Source: The National Institute for Occupational Safety and Health (NIOSH)
- Flash Point: greater than 200 °F (NTP, 1992) Source: CAMEO Chemicals
- Flash Point: 248 °F Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Flash Point: 248 °F (Closed Cup) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 114 °C c.c. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Flash Point: 248 °F Source: Occupational Safety and Health Administration (OSHA)
- Flash Point: 248 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- LogP: 1.12 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: 38.3 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: 3.5 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: 3.5 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: 38 °F Source: Occupational Safety and Health Administration (OSHA)
- Melting Point: 38 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Physical Description: Phenyl glycidyl ether is a colorless liquid. (NTP, 1992) Source: CAMEO Chemicals
- Physical Description: Liquid Source: EPA Chemical Data Reporting (CDR)
- Physical Description: Colorless liquid. [Note: A solid below 38 degrees F.] [NIOSH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Physical Description: Colorless liquid. Source: Occupational Safety and Health Administration (OSHA)
- Physical Description: Colorless liquid. [Note: A solid below 38 °F.] Source: The National Institute for Occupational Safety and Health (NIOSH)
- Refractive Index: Index of refraction = 1.5307 at 21 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: 1 to 5 mg/mL at 64 °F (NTP, 1992) Source: CAMEO Chemicals
- Solubility: 12.9% in octane; completely sol in acetone and toluene Source: Hazardous Substances Data Bank (HSDB)
- Solubility: In water, 2,400 mg/L at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Solubility in water, g/100ml at 20 °C: 0.24 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Solubility: 0.2% Source: The National Institute for Occupational Safety and Health (NIOSH)
- Vapor Pressure: 0.01 mmHg at 68 °F (NTP, 1992) Source: CAMEO Chemicals
- Vapor Pressure: 0.01 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: 1.0X10-2 mm Hg at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: Vapor pressure, Pa at 20 °C: 1.33 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Vapor Pressure: 0.01 mmHg Source: Occupational Safety and Health Administration (OSHA)
- Vapor Pressure: 0.01 mmHg Source: The National Institute for Occupational Safety and Health (NIOSH)
- IARC Carcinogenic Agent: Phenyl glycidyl ether 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 47: (1989) Some Organic Solvents, Resin Monomers and Related Compounds, Pigments and Occupational Exposures in Paint Manufacture and Painting; 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)
- Exposure Routes: The substance can be absorbed into the body by inhalation of its aerosol and through the skin. 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. IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop. Provide proper respiratory protection to rescuers entering an unknow 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: Soap wash promptly - If this chemical contacts the skin, promptly wash the contaminated skin with soap and water. If this chemical penetrates the clothing, promptly remove the clothing and wash the skin with soap and water. Get medical attention promptly.; 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: H315: Causes skin irritation [Warning Skin corrosion/irritation]; H317: May cause an allergic skin reaction [Warning Sensitization, Skin]; H332: Harmful if inhaled [Warning Acute toxicity, inhalation]; H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]; H341: Suspected of causing genetic defects [Warning Germ cell mutagenicity]; H350: May cause cancer [Danger Carcinogenicity]; H412: Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Precautionary Statement Codes: P203, P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P317, P318, P319, P321, P332+P317, P333+P317, P362+P364, P403+P233, 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: H312+H332 (15.6%): Harmful in contact with skin or if inhaled [Warning Acute toxicity, dermal; acute toxicity, inhalation]; H312 (24.6%): Harmful in contact with skin [Warning Acute toxicity, dermal]; H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]; H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]; H319 (18.7%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H332 (99.8%): Harmful if inhaled [Warning Acute toxicity, inhalation]; H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]; H341 (100%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]; H350 (100%): May cause cancer [Danger Carcinogenicity]; H412 (98.4%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P203, P261, P264, P264+P265, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P317, P318, P319, P321, P332+P317, P333+P317, P337+P317, P362+P364, P403+P233, 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 627 reports by companies from 27 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: H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H315: Causes skin irritation [Warning Skin corrosion/irritation]; H317: May cause an allergic skin reaction [Warning Sensitization, Skin]; H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H336: May cause drowsiness or dizziness [Warning Specific target organ toxicity, single exposure; Narcotic effects]; H351: Suspected of causing cancer [Warning Carcinogenicity]; H361: Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]; H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure]; H402: Harmful to aquatic life [Hazardous to the aquatic environment, acute hazard] Source: NITE-CMC
- Precautionary Statement Codes: P203, P260, P261, P264, P264+P265, P270, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P308+P316, P317, P318, P319, P321, P332+P317, P333+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- GHS Hazard Statements: H303: May be harmful if swallowed [Warning Acute toxicity, oral]; H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H315: Causes skin irritation [Warning Skin corrosion/irritation]; H317: May cause an allergic skin reaction [Warning Sensitization, Skin]; H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]; H336: May cause drowsiness or dizziness [Warning Specific target organ toxicity, single exposure; Narcotic effects]; H351: Suspected of causing cancer [Warning Carcinogenicity]; H361: Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]; H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure] Source: NITE-CMC
- Precautionary Statement Codes: P203, P260, P261, P264, P264+P265, P270, P271, P272, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P318, P319, P321, P332+P317, P333+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- Target Organs: Eyes, skin, central nervous system, hematopoietic system, reproductive system Source: The National Institute for Occupational Safety and Health (NIOSH)
- Environmental Bioconcentration: An estimated BCF of 8 was calculated for phenyl glycidyl ether(SRC), using a water solubility of 2,400 mg/L(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), an estimated Koc value of 60(SRC), determined from a water solubility of 2,400 mg/L(2) and a regression-derived equation(3), indicates that phenyl glycidyl ether is expected to have high mobility in soil(SRC). Volatilization of phenyl glycidyl ether from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 8.2X10-7 atm-cu m/mole(SRC), derived from its vapor pressure, 1.0X10-2 mm Hg(2), and water solubility(2). Phenyl glycidyl ether is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(2). A theoretical BOD range from 0 to 6% after 5 days using activated sludge(4,5) indicates that biodegradation may not be an important fate process in soil(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 60(SRC), determined from a water solubility of 2,400 mg/L(2) and a regression-derived equation(3), indicates that phenyl glycidyl ether 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 8.2X10-7 atm-cu m/mole(SRC), derived from its vapor pressure, 1.0X10-2 mm Hg(2), and water solubility(2). Epoxides in general hydrolyze rapidly at 25 °C and pH 7(4) through neutral, acid, or base-mediated reactions(5). Hydrolysis products are usually the corresponding diol and sometimes re-arranged products(5). According to a classification scheme(6), an estimated BCF of 8(SRC), from its water solubility(2) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low(SRC). A theoretical BOD range from 0 to 6% after 5 days using activated sludge(7,8) indicates that biodegradation may not be an important 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), phenyl glycidyl ether, which has a vapor pressure of 1.0X10-2 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase phenyl glycidyl ether 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 13 hrs(SRC), calculated from its rate constant of 2.9X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Phenyl glycidyl ether does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(4). Source: Hazardous Substances Data Bank (HSDB)
- Consumer Uses: Not Known or Reasonably Ascertainable Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Viscosity modifiers Source: EPA Chemical Data Reporting (CDR)
- Sources/Uses: Glycidyl ethers are used as reactive diluents in epoxy resins. [LaDou, p. 550] Allergic contact dermatitis in shoemakers; [Marks] As a reactive diluent in uncured epoxy resins, it reduces viscosity in casting , adhesive and laminating applications; [ACGIH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Industrial Processes with risk of exposure: Plastic Composites Manufacturing [Category: Industry] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: As an acid acceptor it is very effective as a stabilizer of halogenated compounds. Its high solvency for halogenated materials offers many possibilities as an intermediate. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Plasticizer for epoxy resins Source: Hazardous Substances Data Bank (HSDB)
- Uses: Monomer for photoreactive polymers /from table/ Source: Hazardous Substances Data Bank (HSDB)
- Uses: PGE is used as a reactive diluent in uncured epoxy resins to reduce the viscosity of the uncured system for ease in casting, adhesives and laminating applications. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Component of epoxy resins 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 2026-09-02 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Record details
Chemical name
1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether)
Chemical / IUPAC name
Phenylglycidyl ether
Regulatory information
SCCS opinions
- Opinion concerning Chemical Ingredients in Cosmetic Products classified as Carcinogenic, Mutagenic or Toxic to Reproduction according to the Chemicals Directive 67/548/EECC
- Opinion concerning Chemical Ingredients in Cosmetic Products classified as Carcinogenic, Mutagenic or Toxic to Reproduction according to the Chemicals Directive 67/548/EEC
CMR
| Category | Carcinogenic | Mutagenic | Reprotoxic |
|---|---|---|---|
| Cat. 1B | ✓ | — | — |
| Cat. 2 | — | ✓ | — |
Key data
Related records for 1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether)
Direct matches are limited for this record, so nearby entries from Annex II are shown as well.
R-1-Chloro-2,3-epoxypropane
2,3-Epoxypropan-1-ol (Glycidol)
1-Chloro-2,3-epoxypropane (Epichlorohydrin)
(Epoxyethyl)benzene (Styrene oxide)
2,2'-Bioxirane (1,2:3,4-Diepoxybutane)
Methyloxirane (Propylene oxide)
(2RS,3RS)-3-(2-Chlorophenyl)-2-(4-fluorophenyl)-[1H-1,2,4-triazol-1-yl)methyl]oxirane; Epoxiconazole
Bromoethylene (Vinyl bromide)
2-Methoxyethanol [1] and its acetate (2-Methoxyethyl acetate) [2]
What Annex II means for 1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether)
1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether) is listed as a prohibited substance under Annex II of EU Cosmetics Regulation 1223/2009 and must not be intentionally added. Article 17 separately addresses unintended small quantities that are technically unavoidable under good manufacturing practice and compatible with the Article 3 safety requirement.
Formulators must screen their ingredients and raw materials to ensure none contain this substance. Suppliers should provide documentation confirming absence when requested.
The page also surfaces 12 related annex records with overlapping identifiers, annex logic or naming patterns.
Compliance checklist
- Verify this substance is absent from all raw materials and finished formulations.
- Request absence confirmation or CoA from raw material suppliers.
- Document the screening result in the Product Information File (PIF).
- This substance has CMR classification. Review the CMR table above and verify current Annex II/III status before use.
Frequently asked questions
Source note for Annex II record 1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether)
This page summarizes one Annex II record for 1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether) from public European Commission cosmetic materials and adds linked inventory or identifier matches when available.
Use this record page to review Annex II conditions for 1,2-Epoxy-3-phenoxypropane (Phenylglycidyl ether), but confirm any final regulatory decision against the current official annex wording and source files.
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